GB882110A - Esters of thiocarbamic acid - Google Patents

Esters of thiocarbamic acid

Info

Publication number
GB882110A
GB882110A GB6511/58A GB651158A GB882110A GB 882110 A GB882110 A GB 882110A GB 6511/58 A GB6511/58 A GB 6511/58A GB 651158 A GB651158 A GB 651158A GB 882110 A GB882110 A GB 882110A
Authority
GB
United Kingdom
Prior art keywords
formula
group
alkyl
carbon atoms
compounds
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB6511/58A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Monsanto Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Monsanto Chemicals Ltd, Monsanto Chemical Co filed Critical Monsanto Chemicals Ltd
Publication of GB882110A publication Critical patent/GB882110A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
    • C23F11/16Sulfur-containing compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/34Organic compounds containing sulfur

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A detergent composition suitable for removing or preventing the tarnish of silver plate comprises (a) a detergent such as soap, an alkali metal, ammonium, or amine alkylaryl sulphonate, e.g. ammonium dodecylbenzene sulphonate, an alkali metal alkyl sulphate, or an ethylene oxide condensate with an alkylphenol or with tall oil, and (b) thiocarbamic ester of the formula:- <FORM:0882110/III/1> in which R is an organic amino substituent, the nitrogen atom of which is directly linked to the carbonyl carbon atom and to two other carbon atoms, provided that R does not comprise more than one carbocyclic group, and R1 is an unsaturated aliphatic group which does not contain a thiocarbamyl group, but excluding compounds having the formula:- <FORM:0882110/III/2> where R1 is a 2, 3-dichloroallyl group and R2 an R3 are each C1-4 alkyl groups (see Specification 882,111), and also compounds of the formula:- <FORM:0882110/III/3> where R1 is a C2-5 alkenyl group and R2 an R3 are alkyl groups having at least 3 carbon atoms (see Specification 808,753).ALSO:The invention comprises thiocarbamic esters of the formula <FORM:0882110/IV (b)/1> in which R is an organic amino substituent the nitrogen atom of which is directly linked to the carbonyl carbon atom and to two other carbon atoms, provided that R does not comprise more then one carbocyclic group, and R1 is an unsaturated aliphatic group which does not contain a thiocarbamyl group, but excluding compounds having the formula <FORM:0882110/IV (b)/2> where R1 is a 2,3-dichloroalkyl group and R2 and R3 are each C1-4 alkyl groups (see Specification 882,111), and also compounds of the formula <FORM:0882110/IV (b)/3> where R1 is a C2-5 alkenyl group and R2 an R3 are alkyl groups having at least 3 carbon atoms (see Specification 808,753). The substituent R is preferably represented by -NR2R3, where R2 and R3 are each alkyl, cycloalkyl, alkoxy alkyl, aryl, aryloxyalkyl, aralkyl, aralkoxyalkyl, cyanoalkyl, alkenyl, cycloalkenyl or halogenated alkenyl groups, provided not more than one of R2 and R3 represents a cycloalkyl, aryl, aryloxyalkyl, aralkyl or aralkoxyalkyl group, or together represent a polymethylene group which is optionally interrupted by an oxygen or nitrogen atom. The above compounds are prepared by heating an aqueous solution of an alkali metal salt of a thiocarbamic acid of the formula R-CO-S-M (where M represents an alkali metal ion) with a halide of the formula R1-X (where X represents halogen), or by heating an alkyl thionocarbamate of the formula R-CS-O-Alkyl with a halide of the formula R1-X (rearrangement to the corresponding thiocarbamate occurring during the ester interchange. Thiocarbamates of the formula R-CO-S-M are prepared by reacting an amine of the formula R-H with carbon oxysulphide in the presence of aqueous caustic alkali.ALSO:A phytotoxicidal composition having additionally some defoliant and nematoidal activity comprises a thiocarbamic ester of the formula <FORM:0882110/VI/1> in which R is an organic amino substituent the nitrogen atom of which is directly linked to the carbonyl carbon atom and to two other carbon atoms, provided that R does not comprise more than one carbocyclic group, and R1 is an unsaturated aliphatic group which does not contain a thiocarbamyl group, but excluding compounds having the formula <FORM:0882110/VI/2> where R1 is a 2,3-dichloroallyl group and R2 and R3 are each C1-4 alkyl groups (see Specification 882,111), and also compounds of the formula <FORM:0882110/VI/3> where R1 is a C2-5 alkenyl group and R2 and R3 are alkyl groups having at least 3 carbon atoms (see Specification 808,753), together with an inert liquid or finely divided solid diluent and, if desired, a dispersing agent.
GB6511/58A 1957-02-28 1958-02-28 Esters of thiocarbamic acid Expired GB882110A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US882110XA 1957-02-28 1957-02-28

Publications (1)

Publication Number Publication Date
GB882110A true GB882110A (en) 1961-11-15

Family

ID=22210032

Family Applications (1)

Application Number Title Priority Date Filing Date
GB6511/58A Expired GB882110A (en) 1957-02-28 1958-02-28 Esters of thiocarbamic acid

Country Status (1)

Country Link
GB (1) GB882110A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3676479A (en) * 1969-11-10 1972-07-11 Gulf Research Development Co Method of manufacturing allyl n,n-dialkylthiolcarbamates
JPS5028949B1 (en) * 1970-12-12 1975-09-19
US3978107A (en) * 1970-05-09 1976-08-31 Bayer Aktiengesellschaft Novel cyclohexyl carbamates and herbicidal and acaricidal compositions
US3984450A (en) * 1973-07-07 1976-10-05 Basf Aktiengesellschaft Thiolcarbamates
FR2492222A1 (en) * 1980-10-21 1982-04-23 Hodogaya Chemical Co Ltd NEMATOCIDAL AGENTS COMPRISING THIOLCARBAMATE
RU2609122C2 (en) * 2015-07-13 2017-01-30 Общество с ограниченной ответственностью "МИРРИКО" Method of obtainment of bases for corrosion inhibitors of prolonged action for process equipment protection (versions)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3676479A (en) * 1969-11-10 1972-07-11 Gulf Research Development Co Method of manufacturing allyl n,n-dialkylthiolcarbamates
US3978107A (en) * 1970-05-09 1976-08-31 Bayer Aktiengesellschaft Novel cyclohexyl carbamates and herbicidal and acaricidal compositions
JPS5028949B1 (en) * 1970-12-12 1975-09-19
US3984450A (en) * 1973-07-07 1976-10-05 Basf Aktiengesellschaft Thiolcarbamates
FR2492222A1 (en) * 1980-10-21 1982-04-23 Hodogaya Chemical Co Ltd NEMATOCIDAL AGENTS COMPRISING THIOLCARBAMATE
US4696947A (en) * 1980-10-21 1987-09-29 Hodogaya Chemical Co., Ltd. Nematocide
RU2609122C2 (en) * 2015-07-13 2017-01-30 Общество с ограниченной ответственностью "МИРРИКО" Method of obtainment of bases for corrosion inhibitors of prolonged action for process equipment protection (versions)

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