IL29495A - Catechol half esters of beta-haloethylphosphonic acid - Google Patents
Catechol half esters of beta-haloethylphosphonic acidInfo
- Publication number
- IL29495A IL29495A IL29495A IL2949568A IL29495A IL 29495 A IL29495 A IL 29495A IL 29495 A IL29495 A IL 29495A IL 2949568 A IL2949568 A IL 2949568A IL 29495 A IL29495 A IL 29495A
- Authority
- IL
- Israel
- Prior art keywords
- catechol
- beta
- groups
- half esters
- compound
- Prior art date
Links
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 title description 25
- 150000002148 esters Chemical class 0.000 title description 21
- 239000002253 acid Substances 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims description 18
- 125000005843 halogen group Chemical group 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000002790 naphthalenes Chemical class 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 12
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 7
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 244000046052 Phaseolus vulgaris Species 0.000 description 5
- -1 cyclic ester Chemical class 0.000 description 5
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 244000075850 Avena orientalis Species 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 244000299507 Gossypium hirsutum Species 0.000 description 2
- 244000013123 dwarf bean Species 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000008635 plant growth Effects 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 1
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 1
- BFKXVERGWXHHIH-UHFFFAOYSA-N 2-bromoethylphosphonic acid Chemical compound OP(O)(=O)CCBr BFKXVERGWXHHIH-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 235000009432 Gossypium hirsutum Nutrition 0.000 description 1
- 241000209219 Hordeum Species 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 241000735234 Ligustrum Species 0.000 description 1
- 241000576411 Ligustrum ovalifolium Species 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 239000007866 anti-wear additive Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229940125758 compound 15 Drugs 0.000 description 1
- 235000005489 dwarf bean Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- GATNOFPXSDHULC-UHFFFAOYSA-N ethylphosphonic acid Chemical compound CCP(O)(O)=O GATNOFPXSDHULC-UHFFFAOYSA-N 0.000 description 1
- 229960004887 ferric hydroxide Drugs 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- IEECXTSVVFWGSE-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Fe+3] IEECXTSVVFWGSE-UHFFFAOYSA-M 0.000 description 1
- 235000021332 kidney beans Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 238000000954 titration curve Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4084—Esters with hydroxyaryl compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/065—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds containing sulfur
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cultivation Of Plants (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61782067A | 1967-02-23 | 1967-02-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL29495A true IL29495A (en) | 1972-08-30 |
Family
ID=24475196
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL29495A IL29495A (en) | 1967-02-23 | 1968-02-19 | Catechol half esters of beta-haloethylphosphonic acid |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3531549A (de) |
| CH (1) | CH500231A (de) |
| DE (1) | DE1668181B2 (de) |
| FR (1) | FR1556007A (de) |
| GB (1) | GB1219801A (de) |
| IL (1) | IL29495A (de) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1950100B2 (de) * | 1969-10-04 | 1976-12-02 | Bayer Ag, 5090 Leverkusen | Verwendung von 2-chloraethan-(thiono)- phosphonsaeureamido-verbindungen zur beeinflussung des pflanzenwachstums |
| US3907540A (en) * | 1969-10-04 | 1975-09-23 | Bayer Ag | Herbicidal composition and method comploying 2-chloroethane-(thiono)phosphonic acid derivatives |
| US4401454A (en) * | 1969-10-24 | 1983-08-30 | Union Carbide Corporation | Growth regulation methods |
| US3879188A (en) * | 1969-10-24 | 1975-04-22 | Amchem Prod | Growth regulation process |
| US4240819A (en) * | 1972-01-28 | 1980-12-23 | Union Carbide Agricultural Products, Inc. | Method for the inhibition of plant growth |
| US4271072A (en) * | 1977-12-20 | 1981-06-02 | American Hoechst Corporation | Azo dyestuffs containing -SO2 CH2 CH2 OSO3 H and -N(CH2 CH2 OSO3 H)2 groups |
| HU190580B (en) * | 1984-07-18 | 1986-09-29 | Nitrokemia Ipartelepek,Hu | Plant growth regulating compositions comprising phosphonic acid-esters as active substance |
| US5994272A (en) * | 1998-04-14 | 1999-11-30 | Fresh Express Incorporated | Method for inhibition of head formation in lettuce |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3118876A (en) * | 1958-07-26 | 1964-01-21 | Takeda Pharmaceutical | Process for preparing glycoside phosphates |
-
1967
- 1967-02-23 US US617820A patent/US3531549A/en not_active Expired - Lifetime
-
1968
- 1968-02-16 DE DE1668181A patent/DE1668181B2/de not_active Ceased
- 1968-02-19 CH CH234768A patent/CH500231A/de not_active IP Right Cessation
- 1968-02-19 IL IL29495A patent/IL29495A/en unknown
- 1968-02-22 GB GB8757/68A patent/GB1219801A/en not_active Expired
- 1968-02-23 FR FR1556007D patent/FR1556007A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CH500231A (de) | 1970-12-15 |
| FR1556007A (de) | 1969-01-31 |
| US3531549A (en) | 1970-09-29 |
| GB1219801A (en) | 1971-01-20 |
| DE1668181A1 (de) | 1971-08-05 |
| DE1668181B2 (de) | 1975-12-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0262209B1 (de) | Synergetische pflanzenwuchsregulatorzusammensetzung | |
| US4270948A (en) | Herbicidal compound, herbicidal composition containing the same, and method of use thereof | |
| JP2693774B2 (ja) | マロン酸誘導体化合物の植物の成長を抑制するための使用 | |
| EP0109314A1 (de) | Aluminium N-Phosphonomethylglyzin und seine Verwendung als Herbizid | |
| IE51852B1 (en) | Trialkylsulfonium and trialkylsulfoxonium salts of n-phosphonomethylglycine,production thereof,their use as plant growth regulators and herbicides and compositions containing them | |
| IL47972A (en) | N-phosphonomethylglycines and herbicidal compositions containing them | |
| US4384880A (en) | Trialkylsulfonium salts of N-phosphonomethyl-glycine and their use as plant growth regulators and herbicides | |
| US4525202A (en) | Phosphonium salts of N-phosphonomethylglycine and their use as herbicides and plant growth regulants | |
| US3531549A (en) | Catechol half esters of beta-haloethylphosphonic acid | |
| US3551528A (en) | Phosphonic acid esters and the methol for their preparation | |
| US3223514A (en) | Process for the control of plant growth | |
| US4415503A (en) | Method for preparation of N-phosphonomethylglycine | |
| US4018854A (en) | Carboxyphosphonates | |
| EP0105262A1 (de) | Tetrasubstituiertes ammoniumsalz aus n-phosphonomethylglycin und dessen verwendung als herbizide und pflanzenwachstumsregler | |
| US3562363A (en) | O-catechol o-hydrocarbyl-vinyl phosphonates and process for making same | |
| GB631549A (en) | Improvements in or relating to the manufacture of compounds containing phosphorus having insecticidal properties | |
| US4191552A (en) | Amine salts of substituted N-phosphonomethylureas and their use as plant growth regulators | |
| US4376644A (en) | Tri-mixed alkylsulfonium salts of N-phosphonomethylglycine and their use as plant growth regulators and herbicides | |
| CA1131654A (en) | Ester derivatives of n-trifluoroacetyl-n- phosphonomethylglycine and the herbicidal use thereof | |
| US3388150A (en) | Fluoroketone hemiketal esters | |
| CA1122995A (en) | Amide and hydrazide derivatives of n-trifluoroacetyl-n-phosphonomethylglycine | |
| CA1134383A (en) | Derivatives of n-trifluoroacetyl-n- phosphonomethylglycine dichloride | |
| US3432495A (en) | Aryl hydroxyalkyl arsinic acids and salts thereof | |
| EP0068732B1 (de) | Herbizid wirkende Monoester und Diester von N-alkyl substituierten Amino-Methyl Phosphonsäuren und Verfahren zu ihrer Herstellung | |
| US4328027A (en) | Di-triethylamine salt of N,N'-bis-carboethoxymethyl-N,N'-bis-phosphonomethylurea and its use as a plant growth regulator |