CAS 2432-77-1

Hexanethioic acid, S-methyl ester

Description:

Hexanethioic acid, S-methyl ester, is an organic compound characterized by its structure, which includes a hexane backbone with a thioic acid functional group and a methyl ester. This compound typically appears as a colorless to pale yellow liquid with a distinct odor. It is soluble in organic solvents and exhibits moderate polarity due to the presence of the ester and thioic acid functionalities. Hexanethioic acid, S-methyl ester is known for its reactivity, particularly in nucleophilic substitution reactions, owing to the presence of the ester group. It can participate in various chemical reactions, including hydrolysis and transesterification. The compound is utilized in organic synthesis and may serve as an intermediate in the production of other chemical entities. Safety considerations should be taken into account when handling this substance, as it may pose risks such as skin and eye irritation. Proper storage in a cool, dry place away from incompatible materials is recommended to maintain its stability and integrity.

Formula: C₇H₁₄OS

InChI: InChI=1S/C7H14OS/c1-3-4-5-6-7(8)9-2/h3-6H2,1-2H3

InChI key: InChIKey=AKGAHYLJHAOPKQ-UHFFFAOYSA-N

SMILES: C(CCCCC)(SC)=O

Synonyms:

• 1-(Methylsulfanyl)hexan-1-one
• Hexanethioic acid, S-methyl ester
• Methanethiol caproate
• S-Methyl thiohexanoate
• S-Methyl hexanethioate
• S-Methyl hexanethioate

S-Methyl hexanethioate

CAS: 2432-77-1

S-Methyl hexanethioate

Purity: 95%

Molecular weight: 146.25g/mol

Ref: 54-OR1073710

S-Methyl thiohexanoate

CAS: 2432-77-1

S-Methyl thiohexanoate is a fatty acid that is the product of the serine protease activity of the potato tuber. It has been shown to have a transcriptional regulatory effect on carbon source utilization and natural compounds production, which may be due to its ability to alter the phospholipid composition in plant cells. S-Methyl thiohexanoate can inhibit or induce natural compounds production depending on the concentration used. The effects of this compound are mediated by its ability to form hydrogen bonds with hydroxyl groups in phospholipids, altering their configuration and consequently disrupting membrane integrity. S-Methyl thiohexanoate also has been shown to act as an electron donor for covalent polymerization reactions catalyzed by DNA polymerases and reverse transcriptases. This may be due to its ability to form hydrogen bonds with phosphate groups in nucleic acids, altering their configuration and consequently disrupting DNA or RNA synthesis.

Formula: C₇H₁₄OS

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 146.25 g/mol

Ref: 3D-FM35693