benzyl thioacetate

ethanethioic acid S-(phenylmethyl) ester

CAS: 32362-99-5 C9 H10 O S MW: 166.24290000

Identification

Namebenzyl thioacetate
CAS Number32362-99-5
FDA UNIISearch
Molecular FormulaC9 H10 O S
Molecular Weight166.24290000
Nikkaji NumberJ427.447D

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 238.00 to 239.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure 0.028000 mmHg @ 25.00 °C. (est)
Flash Point 210.00 °F. TCC ( 98.80 °C. ) (est)
logP (o/w) 2.342 (est)
Soluble in alcohol
Insoluble in water

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryinformation only not used for fragrances or flavors
Recommendation for benzyl thioacetate usage levels up tonot for fragrance use.
Recommendation for benzyl thioacetate flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

S- benzyl ethane thioate S- benzyl ethanethioate S- benzylthioacetate ethanethioic acid S-(phenylmethyl) ester thio-aceticacid S-benzyl ester (6CI,7CI,8CI) PubMed: Chemotactic effect of odorants and tastants on the ciliate Tetrahymena pyriformis. PubMed: Palladium-catalyzed cross-coupling of benzyl thioacetates and aryl halides. PubMed: Competitive reaction pathways for o-anilide aryl radicals: 1,5- or 1,6-hydrogen transfer versus nucleophilic coupling reactions. A novel rearrangement to afford an amidyl radical. PubMed: Rapid proton-coupled electron-transfer of hydroquinone through phenylenevinylene bridges. PubMed: Acetyl benzyl disulfide. PubMed: Synthesis and biological activities of N-acetyl-1-thiomuramoyl-L-alanyl-D-isoglutamine and some of its lipophilic derivatives.