5697-20-1 Usage
Description
2-Sulfanylbenzamide, also known as 2-Mercaptobenzamide or o-Mercaptobenzamide, is a chemical compound with the molecular formula C7H7NOS. It is a white to off-white crystalline powder that is widely used in various industries.
Used in Pharmaceutical Industry:
2-Sulfanylbenzamide is used as an intermediate in the production of various drugs and pharmaceuticals for its ability to be synthesized into other organic compounds.
Used in Dye and Pigment Manufacturing:
2-Sulfanylbenzamide is used as a key component in the manufacturing of dyes and pigments due to its chemical properties that contribute to color development.
Safety Note:
2-Sulfanylbenzamide is considered to be relatively stable under normal conditions, but it should be handled and stored with care due to its potential for causing irritation to the skin, eyes, and respiratory tract.
Check Digit Verification of cas no
The CAS Registry Mumber 5697-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5697-20:
(6*5)+(5*6)+(4*9)+(3*7)+(2*2)+(1*0)=121
121 % 10 = 1
So 5697-20-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NOS/c8-7(9)5-3-1-2-4-6(5)10/h1-4,10H,(H2,8,9)
5697-20-1Relevant articles and documents
PROCESS FOR PREPARING 1,2-BENZOISOTHIAZOLIN-3-ONES
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Paragraph 0024-0031, (2014/10/29)
Sodium sulfide hydrate is at least partially dehydrated by heating with N-methyl 2-pyrrolidone. 2-Chlorobenzamide is added to the mixture which is heated further. The mixture is cooled and treated with aqueous hydrogen peroxide to give the sodium salt of 1,2-benzisothiazolin-3-one in good yield. Acidification if desired gives rise to the free 1,2-benzisothiazolin-3-one.
The Stereochemistry of Organometallic Compounds. XLIV* Rhodium-Catalysed Hydroformylation of Some Alkenylthio Aromatic Compounds
Campi, Eva M.,Roy Jackson,Trnacek, Andrew E.
, p. 807 - 812 (2007/10/03)
Rhodium-catalysed reactions of o-[(allyl and butenyl)thio] benzonitriles and benzamides with H2/CO give quantitative yields of aldehydes whereas the corresponding benzylamines give only polymeric material. The results are compared with reactions of the analogous alkenylamines and alkenyloxy compounds.