TH1950A - Pirazine compounds, their preparations and uses, mixtures containing them and methods for stopping unwanted plant growth. - Google Patents
Pirazine compounds, their preparations and uses, mixtures containing them and methods for stopping unwanted plant growth.Info
- Publication number
- TH1950A TH1950A TH8401000194A TH8401000194A TH1950A TH 1950 A TH1950 A TH 1950A TH 8401000194 A TH8401000194 A TH 8401000194A TH 8401000194 A TH8401000194 A TH 8401000194A TH 1950 A TH1950 A TH 1950A
- Authority
- TH
- Thailand
- Prior art keywords
- atoms
- compounds
- group
- aerobic
- carbon atoms
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract 11
- 238000000034 method Methods 0.000 title claims 3
- 239000000203 mixture Substances 0.000 title claims 2
- 230000008635 plant growth Effects 0.000 title claims 2
- 238000002360 preparation method Methods 0.000 title 1
- 125000004429 atom Chemical group 0.000 claims abstract 7
- 239000000126 substance Substances 0.000 claims abstract 7
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract 4
- 125000005842 heteroatom Chemical group 0.000 claims abstract 4
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 4
- 239000001301 oxygen Substances 0.000 claims abstract 4
- 239000011593 sulfur Chemical group 0.000 claims abstract 4
- 229910052717 sulfur Chemical group 0.000 claims abstract 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract 3
- 125000005843 halogen group Chemical group 0.000 claims abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052794 bromium Inorganic materials 0.000 claims abstract 2
- 229910052799 carbon Inorganic materials 0.000 claims abstract 2
- 229910052801 chlorine Inorganic materials 0.000 claims abstract 2
- 239000000460 chlorine Substances 0.000 claims abstract 2
- 229910052731 fluorine Inorganic materials 0.000 claims abstract 2
- 239000011737 fluorine Substances 0.000 claims abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 2
- 125000001624 naphthyl group Chemical group 0.000 claims abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract 2
- 239000004009 herbicide Substances 0.000 claims 2
- JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- NYGHGTMKALXFIA-UHFFFAOYSA-N azapetine Chemical compound C1N(CC=C)CC2=CC=CC=C2C2=CC=CC=C21 NYGHGTMKALXFIA-UHFFFAOYSA-N 0.000 claims 1
- 229960004779 azapetine Drugs 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 claims 1
- 229960003495 thiamine Drugs 0.000 claims 1
- 235000019157 thiamine Nutrition 0.000 claims 1
- 239000011721 thiamine Substances 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 abstract 1
- 230000000423 heterosexual effect Effects 0.000 abstract 1
- 230000002147 killing effect Effects 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
Abstract
สารประกอบพิราซีนที่มีสูตรทั่วไป (I) (สูตรเคมี) ซึ่ง X แทนออกซิเจน หรือกำมะถัน, R แทนไฮโดรเจน อะตอม หรือแอมโมเนียม แอลคิลที่มีคาร์บอนได้สูงถึง 6 อะตอม, หมู่เฟนิล หรือ เบนซิล, และ Y แทนหมู่แอโรมาทิค ที่เลือกได้จากเฟนิล, แนฟธิล และแอนธริล, หรือหมู่เฮเทอโรแอโร แอโรมาทิคที่มีอะตอมในริง 5 ถึง 6 อะตอม ซึ่งมีเฮเทอโรอะตอมได้สูงถึง 3 อะตอม ที่เลือกได้จากไนโตรเจน, ออกซิเจน และกำมะถัน,หมู่แอโรมาทิค หรือเฮเทอโรแอโรมาทิค ดังกล่าวไม่เป็นชนิดที่ถูกแทนที่หรือเป็นชนิดที่ถูกแทนที่ ได้โดยหมู่แทนที่ 1 หรือ 2 หมู่ ที่อิสระต่อกันซึ่งเลือกได้จาก ไซแอโน, เฮโล,อะมิโน, ไบโทร, แอลคอกซิที่มีคาร์บอนได้สูงถึง 4 อะตอม,เฮโลแอลคอกซิ และเฮโลแอลคิลที่มีคาร์บอนได้สูงถึง4 อะตอม แลมีโบรมีน, คลอรีน หรือฟลูออรีนได้สูงถึง 4 อะตอม และแอลคิลที่มีคาร์บอนได้สูงถึง 4 อะตอม หรือที่ตำแหน่งอยู่ติดๆ กันโดยหมู่ชนิดไบวาเลนท์ (สูตรเคมี) ซึ่ง n เป็น 1 หรือ 2 มีคุณสมบัติฆ่าวัชพืชซึ่งใช้เป็นประโยชน์ได้ Pirazine compound with the general formula (I) (chemical formula), where X represents oxygen or sulfur, R represents the hydrogen atom or ammonium. 6 carbon atoms alkyl, phenyl or benzyl group, and Y represents the aerobic group. Selectable from phenyl, naphthyl and anthril, or heteroero Aerobic with 5 to 6 ring atoms, up to 3 heterosexual atoms, selectable from nitrogen, oxygen and sulfur, aerobic groups. Or hetero aerobic It is neither a type that is replaced nor is it a type that is replaced. Can be by either one or two independent substituting groups, which can be selected from xyano, halo, amino, bitro, alcoxin with up to 4 carbon atoms, heloalcoxin And up to 4 carbon atoms of heloalkyls and up to 4 atoms of bromine, chlorine or fluorine and 4 atoms of alkyl with carbon or adjacent positions. The bivalent group (chemical formula), where n is 1 or 2, has useful weed killing properties.
Claims (1)
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TH1950A true TH1950A (en) | 1984-11-01 |
| TH3028B TH3028B (en) | 1992-08-07 |
Family
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