5331-30-6

Basic information

• Product Name: methyl 3-[(2-hydroxyethyl)sulfanyl]propanoate
• CAS NO: 5331-30-6
• Molecular Formula: C₆H₁₂O₃S
• Molecular Weight: 164.2227
• Mol File: 5331-30-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 276.6°C at 760 mmHg
• Flash Point: 121.1°C
• Density: 1.152g/cm³
• Vapor Pressure: 0.000593mmHg at 25°C
• Refractive Index: 1.489
• CAS DataBase Reference: methyl 3-[(2-hydroxyethyl)sulfanyl]propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-[(2-hydroxyethyl)sulfanyl]propanoate(5331-30-6)
• EPA Substance Registry System: methyl 3-[(2-hydroxyethyl)sulfanyl]propanoate(5331-30-6)

Safety Data

• Hazardous Substances Data: 5331-30-6(Hazardous Substances Data)

Upstream product

• 2935-90-2 Methyl 3-mercaptopropionate 
• 540-51-2 2-bromoethanol 
• 292638-85-8 acrylic acid methyl ester 
• 60-24-2 2-hydroxyethanethiol 
• 100-85-6 N-benzyl-trimethylammonium hydroxide 

Downstream Products

• 5323-60-4 1,6-dihydroxy-3-thiahexane 

Relevant articles and documents

NOVEL DENTAL COMPOSITES SYSTEMS AND METHODS OF MAKING THE SAME AND USING SAME

The invention includes a composition comprising a vinyl sulfone monomer, a thiol monomer, and optionally an isocyanate monomer. The invention further includes a composition comprising a composition comprising the tetra(2-mercapto)silane (SiTSH) monomer an

Synthesis of four glycosides of a disaccharide fragment representing the terminus of the O-polysaccharide of Vibrio cholerae O:1, serotype Inaba, bearing aglycons suitable for linking to proteins

Methyl 4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside was converted into the crystalline 2-(trimethylsilyl)ethyl 4-azido-2-O-benzoyl-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside. Debenzoylation of the latter, followed by glycosylation of the resulting 2-hydroxy derivative with 2-O-acetyl-4-azido-4,6-dideoxy-α-D-mannopyranosyl chloride, gave the 2-(trimethylsilyl)ethyl glycoside of the corresponding disaccharide (8). Deacetylation of 8, followed by reduction of the resulting 4-azido-2-hydroxy derivative with H2S, gave the corresponding amine 10. The latter was treated with 4-O-benzyl-3-deoxy-L-glycero-tetronic acid to give, after debenzylation and acetylation, the fully protected 2-(trimethylsilyl)ethyl α-glycoside of the disaccharide fragment of the O-PS of Vibrio cholerae O:1, serotype Inaba (13). Compound 13 was transformed into the corresponding 1-trichloroacetimidate which was treated, separately, with methyl 6-hydroxyhexanoate and 2-(2-methoxycarbonylethylthio)ethanol, to give two analogs of 13 possessing a differing linkage arm, namely the methyl esters 16 and 17. Each of 16 and 17 was treated with aqueous sodium hydroxide, followed by a cation-exchange resin, to give the two corresponding carboxylic acids (19 and 22). Alternately, treatment of 16 and 17 with hydrazine hydrate gave the acid hydrazides 20 and 23.

Immersion oil containing aliphatic thio compounds

Immersion oils containing aliphatic thio compounds are described. The oils have optical properties and are useful in immersion optics such as fluorescence microscopy.