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1741-83-9

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  • BEST PRICE/ Pentane,1-(methylthio)- CAS NO.1741-83-9

    Cas No: 1741-83-9

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1741-83-9 Usage

General Description

Amyl methyl sulfide is a chemical compound with the molecular formula C6H14S. It is a clear, colorless liquid with a strong, unpleasant odor. Amyl methyl sulfide is commonly used as a flavor and fragrance additive in various food and cosmetic products. It is also used as a solvent and in the production of other chemicals. In addition to its industrial applications, amyl methyl sulfide has been identified as a natural component of certain foods, such as onions and garlic, and has been found to contribute to the characteristic flavors and aromas of these products. However, it should be handled with caution, as exposure to high levels of amyl methyl sulfide can cause irritation to the eyes, skin, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 1741-83-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1741-83:
(6*1)+(5*7)+(4*4)+(3*1)+(2*8)+(1*3)=79
79 % 10 = 9
So 1741-83-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H14S2/c1-3-4-5-6-8-7-2/h3-6H2,1-2H3

1741-83-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Amyl Methyl Sulfide

1.2 Other means of identification

Product number -
Other names 1-methylsulfanylpentane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1741-83-9 SDS

1741-83-9Relevant articles and documents

Silica-promoted facile synthesis of thioesters and thioethers: A highly efficient, reusable and environmentally safe solid support

Basu, Basudeb,Paul, Susmita,Nanda, Ashis K.

experimental part, p. 767 - 771 (2010/09/05)

An efficient, mild and rapid procedure for the acylation and alkylation of aromatic and aliphatic thiols mediated on a silica gel surface at room temperature is described. The protocol allows the protection of thiols under neutral heterogeneous conditions without requiring any bases or Lewis acids, and the silica gel used as the promoter can be recycled for several runs without any loss of activity.

New Oxyfunctionalization Capabilities for ω-Hydroxylases: Asymmetric Aliphatic Sulfoxidation and Branched Ether Demethylation

Katopodis, Andreas G.,Smith, Homer A.,May, Sheldon W.

, p. 897 - 899 (2007/10/02)

Due to inherent difficulties in the chemical generation of aliphatic synthons, the stereo- and regioselective oxyfunctionalization of simple aliphatic substrates represents an area where chemical applications of biocatalysis would be particularly useful.The hydrocarbon monooxygenase from Pseudomonas oleovorans is a prototypical "ω-hydroxylase" known to carry out hydroxylation at the terminal methyl of alkanes as well as epoxidation of terminal olefins.It is now demonstrated that this enzyme system catalyzes stereoselective sulfoxidation of methyl thioether substrates, representing the first clear example of oxygenase-produced chiral aliphatic sulfoxides yet reported.In addition, it is shown that this enzyme system catalyzes oxygenative O-demethylation of branched alkyl methyl and branched vinyl methyl ethers to secondary alcohols and ketones, respectively.These findings establish new oxyfunctionalization capabilities, and thus a significantly expanded biotechnological potential, for the hydrocarbon monooxygenases.

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