S-Ethyl thioacetate

CAS : 625-60-5

Ref. 3D-FE35689

Informations sur le produit

• Nom: S-Ethyl thioacetate
• Synonymes: 1-(Ethylsulfanyl)ethan-1-one, Acetic acid, thio-, S-ethyl ester, Acetic acid, thio-, ethyl ester, Ethanethioic Acid S-Ethyl Ester, Ethanethioic acid, ethyl ester, Ethanethiol, acetate, Ethyl ethanethioate, Ethyl thiolacetate, O-ethyl ethanethioate, S-Ethyl thiolacetate, S-ethyl ethanethioate, S-ethyl ethanethoate, S-ethylthioacetate, Thioacetic acid S-ethyl ester
• CAS: 625-60-5

Description

S-Ethyl thioacetate is an organic compound with the molecular formula CH2SO3CH2CH3. It is a colorless liquid with a pleasant odor. S-Ethyl thioacetate has been shown to be a good nucleophile and reacts quickly with ethyl bromoacetate to form the symmetrical adduct, ethyl 2-(S-ethylthio) acetate. The reaction mechanism for this reaction is believed to involve a concerted, nucleophilic attack of the sulfur atom on the electrophilic carbonyl carbon in ethyl bromoacetate, followed by displacement of the leaving group (Br) by the oxygen atom from S-ethylthio acetate. This leads to formation of an acetic acid derivative that contains two methyl ketones in place of two hydroxyl groups. Glyceraldehyde phosphate dehydrogenase is an enzyme that catalyzes a reaction in which glyceraldehyde 3-phosphate

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 104.17 g/mol
• Formule: C₄H₈OS
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C4H8OS/c1-3-6-4(2)5/h3H2,1-2H3
• Code InChI: InChIKey=APTGPWJUOYMUCE-UHFFFAOYSA-N
• SMILES: CCSC(C)=O