57523-13-4

Basic information

• Product Name: (3-Methylthietan-3-yl)methanol
• Synonyms: (3-Methylthietan-3-yl)methanol;(3-methyl-3-thietanyl)methanol
• CAS NO: 57523-13-4
• Molecular Formula: C₅H₁₀OS
• Molecular Weight: 118.1973
• Mol File: 57523-13-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3-Methylthietan-3-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3-Methylthietan-3-yl)methanol(57523-13-4)
• EPA Substance Registry System: (3-Methylthietan-3-yl)methanol(57523-13-4)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 3
• Hazardous Substances Data: 57523-13-4(Hazardous Substances Data)

Usage

Description

(3-Methylthietan-3-yl)methanol, also known as MTM, is a colorless, volatile liquid with the molecular formula C6H14OS. It is a chemical compound that possesses a pleasant, fruity odor and is commonly used as a flavoring agent in food and beverages.

Uses

Used in Food and Beverage Industry:
(3-Methylthietan-3-yl)methanol is used as a flavoring agent for its pleasant, fruity odor, enhancing the taste and aroma of various food and drink products.
Used in Fragrance and Perfume Industry:
(3-Methylthietan-3-yl)methanol is used as a solvent and in the production of fragrances and perfumes, contributing to the creation of various scents and aromas.
It is important to use (3-Methylthietan-3-yl)methanol in moderation and to be aware of any potential allergic reactions or sensitivities to the compound.

Upstream product

• 77-85-0 2-(hydroxymethyl)-2-methylpropane-1,3-diol 

Downstream Products

• 175222-26-1 3--3-methylthietan 
• 175222-27-2 3-(Diphenylphosphanylmethyl)-3-methylthietan 
• 175222-28-3 3-(Benzylsulfanylmethyl)-3-methylthietan 
• 161202-62-6 3-diphenylphosphanyl-2-diphenylphosphanylmethyl-2-methyl-1-propanethiol 

Relevant articles and documents

SUBSTITUTED IMIDAZOLECARBOXYLATE DERIVATIVES AND THE USE THEREOF

A compound is shown in formula (I). The derivatives of the compound include a stereoisomer, a pharmaceutically acceptable salt, a solvate, a prodrug, a metabolite, a deuterated derivative. The compound is a structurally novel substituted imidazole formate derivative. Substituted imidazole formate derivatives are used in preparing a drug with sedative, hypnotic and/or anesthetic effects, as well as a drug that can control the state of epilepsy. The compound has a good inhibitory effect on the central nervous system, and provides a new option for clinical screening of and/or preparation of a drug with sedative, hypnotic and/or anesthetic effects and controlling the state of epilepsy.

Study of Effects on the Coordination of Thioether Ligands, 2. Stereospecific Ligand Substitutions in Manganese (I) Complexes

Treatment of fac- and fac- with silver hexafluorophosphate yields the η3-tripodal manganese complexes PF6 (7) and PF6 (9), respectively, whereas the reaction of CH3C(CH2PPh2)2(CH2SH) with Mn(CO)5Br gives directly Mn(CO)3 (11).Both ionic complexes 7 and 9 undergo stereospecifically ligand substitution upon treatment with Br(-), I(-), N3(-), SCN(-) and CN(-) to give syn-fac- and syn-fac- (X = Br, I, SCN, N3, CN) respectively, but the neutral complex 11 fails to undergo such a substitution reaction with these ions.However, reaction of I(-) with the complex Mn(CO)3>BF4 (20) , which is obtained from the S-alkylation of 11 with the (CH3)3OBF4, affords syn-fac-Mn(CO)3I (22s) exclusively.The possible reaction mechanism of this ligand substitution is discusssed. - Key Words: Tripodal ligands/ Phosphane ligands/ Thioethers/ Manganese complexes