3201-48-7 Usage
Uses
Used in Agricultural Industry:
BENZOYLTHIO-O-METHYL ESTER CARBAMIC ACID is used as a pesticide or herbicide for its potential to control pests and unwanted plant growth. The carbamate functional group in BENZOYLTHIO-O-METHYL ESTER CARBAMIC ACID is known to possess insecticidal and acaricidal properties, making it a valuable tool in managing agricultural pests and ensuring crop protection.
Used in Pharmaceutical Industry:
BENZOYLTHIO-O-METHYL ESTER CARBAMIC ACID is used as a precursor in the synthesis of pharmaceutical compounds. Its potential anti-fungal activity suggests that it could be a key component in developing new treatments for fungal infections, contributing to the advancement of medicine in this area.
Used in Chemical Research:
BENZOYLTHIO-O-METHYL ESTER CARBAMIC ACID serves as an important target for chemical synthesis and further research. Its unique structure and properties make it a valuable subject for exploration, with the aim of discovering additional applications in various fields, including but not limited to agriculture and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 3201-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,0 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3201-48:
(6*3)+(5*2)+(4*0)+(3*1)+(2*4)+(1*8)=47
47 % 10 = 7
So 3201-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO2S/c1-12-9(13)10-8(11)7-5-3-2-4-6-7/h2-6H,1H3,(H,10,11,13)
3201-48-7Relevant academic research and scientific papers
Ligand Properties of N-Acyl-thiocarbamic-O-alkylesters - A New Class of Aza-analogous 1,3-Thioxoketones
Schroeder, U.,Beyer, L.,Dietze, F.,Richter, R.,Schmidt, Sylke,Hoyer, E.
, p. 184 - 188 (2007/10/02)
A series of six N-benzoyl-thiocarbamic-O-alkylesters (R=Me, Et, i-Pr, Benzyl, n-Hex, n-Dodec; 1-6) has been prepared and characterized.They are weak monoprotic acids.The compounds behave as fairly stable and versatile bidentate (O,S)-chelating ligands towards multivalent metal ions e.g.Ni(II), Cu(II), Pb(II) the stability constants of which have been determined in 75 volpercent dioxane/water.The molecular structure of bis(O-ethyl-N-benzoylthiocarbamato)nickel(II) 2a is presented.The coordination of the nickel atom is square planar with the two sulphur atoms in cis position.
Synthesis of N-acyl-1,3-oxathiol-2-imines
Kulka, Marshall
, p. 1557 - 1559 (2007/10/02)
A facile synthesis of N-acyl-1,3-oxathiol-2-imines, 7, is reported.It comprises the reaction of O-alkyl acylcarbamothioates, 4, with 2-chloroketones in the presence of alcoholic sodium alkoxide.The resulting O-alkyl-S-substituted-N-acylcarbonimidothiates, 6, undergo cyclization with elimination of alcohol, spontaneously, or upon heating in boiling toluene to form 7.
