20600-61-7

Basic information

• Product Name: (butylthio)acetic acid
• Synonyms: (butylthio)acetic acid;NSC75120;Einecs 243-907-9
• CAS NO: 20600-61-7
• Molecular Formula: C₆H₁₂O₂S
• Molecular Weight: 148.22328
• EINECS: 243-907-9
• Mol File: 20600-61-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 247.7°Cat760mmHg
• Flash Point: 103.6°C
• Appearance: /
• Density: 1.088g/cm³
• Vapor Pressure: 0.00814mmHg at 25°C
• Refractive Index: 1.49
• CAS DataBase Reference: (butylthio)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (butylthio)acetic acid(20600-61-7)
• EPA Substance Registry System: (butylthio)acetic acid(20600-61-7)

Safety Data

• Hazardous Substances Data: 20600-61-7(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 72, p. 1073, 1950 DOI: 10.1021/ja01159a005

InChI:InChI=1/C6H12O2S/c1-2-3-4-9-5-6(7)8/h2-5H2,1H3,(H,7,8)

Upstream product

• 4779-86-6 sodium 1-buthanethiolate 
• 3926-62-3 sodium monochloroacetic acid 
• 109-65-9 1-bromo-butane 
• 68-11-1 mercaptoacetic acid 
• 109-79-5 n-butanethiol 
• 144-49-0 Fluoroacetic acid 
• 109-69-3 n-Butyl chloride 
• 78651-86-2 N-pentyl-2-butylthioethanamide 
• 542-69-8 1-iodo-butane 
• 35350-46-0 2,2-dimethyl-1,3oxathiolan-5-one 
• 79-11-8 chloroacetic acid 

Downstream Products

• 58992-42-0 (C₆H₅)3Bi(OOCCH₂S(n-C₄H₉))2 
• 636-70-4 triethylamine hydrobromide 
• 10309-14-5 methyl 2-(butylthio)acetate 

Relevant articles and documents

-

-

COMPOSITIONS, SYNTHESIS, AND METHODS OF USING PHENYLCYCLOALKYLMETHYLAMINE DERIVATIVES

The present invention provides novel phenylcycloalkylmethylamme derivatives, and methods of preparing phenylcycloalkylmethylamme derivatives. The present invention also provides methods of using phenylcycloalkylmethylamme derivatives and compositions of phenylcycloalkylmethylamme derivatives. The pharmaceutical compositions of the compounds of the present invention can be used for treating and/or preventing obesity and obesity related co- morbid indications and depression and depression related co-morbid indications.

Studies on fused β-lactams: Synthesis, stereochemistry and antimicrobial activity of some new cepham analogues

β-Lactam ring has been conveniently grafted onto 2-phenyl-5,6-dihydro-1,3-thiazine 1 by annelating it with in situ prepared ketenes to furnish cepham analogues 6-9. A variety of acids such as menthoxy acetic acid 2, butylthioacetic acid 3, chloroacetic acid 4 and benzotriazole acetic acid 5 have been used as mixed sulphonic acid anhydrides for the cycloaddition reaction. All the compounds have been screened for their antibacterial activities.