1534-08-3 | S-Methyl thioacetate

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$18.00	$12.00
5g	95%	in stock	$36.00	$25.00
25g	95%	in stock	$169.00	$119.00
100g	95%	in stock	$598.00	$419.00

Description

• Catalog Number: AB79009
• Chemical Name: S-Methyl thioacetate
• CAS Number: 1534-08-3
• Molecular Formula: C3H6OS
• Molecular Weight: 90.1441
• MDL Number: MFCD00014989
• SMILES: CSC(=O)C

Computed Properties

• Complexity: 42.2
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 5
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 0.7

Literature

• Theoretical study on the alkaline hydrolysis of methyl thioacetate in aqueous solution.

  The journal of physical chemistry. A 20111124

• The relative rates of thiol-thioester exchange and hydrolysis for alkyl and aryl thioalkanoates in water.

  Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life 20111001

• HeI photoelectron and valence synchrotron photoionization studies of the thioester molecule CH3C(O)SCH3: evidence of vibronic structure.

  The journal of physical chemistry. A 20080703

• The effect of cysteine on production of volatile sulphur compounds by cheese-ripening bacteria.

  International journal of food microbiology 20080320

• Ionization of zwitterionic amine substrates bound to monomeric sarcosine oxidase.

  Biochemistry 20051227

• On the origins of cells: a hypothesis for the evolutionary transitions from abiotic geochemistry to chemoautotrophic prokaryotes, and from prokaryotes to nucleated cells.

  Philosophical transactions of the Royal Society of London. Series B, Biological sciences 20030129

• Synthesis and structure of preorganized, C(3)-symmetric trilactam scaffolds with convergently oriented (S)-acetylthiomethyl appendages.

  Organic letters 20020627

• Production of volatile compounds by cheese-ripening yeasts: requirement for a methanethiol donor for S-methyl thioacetate synthesis by Kluyveromyces lactis.

  Applied microbiology and biotechnology 20020301

• Understanding the relative acyl-transfer reactivity of oxoesters and thioesters: computational analysis of transition state delocalization effects.

  Journal of the American Chemical Society 20011107

• Organization of the multiple coenzymes and subunits and role of the covalent flavin link in the complex heterotetrameric sarcosine oxidase.

  Biochemistry 20010508