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1-Bromo-8-(methylthio)octane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64053-04-9

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64053-04-9 Usage

Chemical structure

A long chain of carbon atoms with a bromine substituent and a methylthio group attached to the eighth carbon atom.

Usage

Used in organic synthesis as a reagent for the introduction of the bromine atom into organic molecules.

Applications

Mainly used in the production of pharmaceuticals and agrochemicals, as well as in the synthesis of other organic compounds.

Safety precautions

Potentially hazardous chemical that can cause skin and eye irritation, and respiratory issues if inhaled.

Handling

Proper safety measures and equipment should be used when handling 1-Bromo-8-(methylthio)octane.

Check Digit Verification of cas no

The CAS Registry Mumber 64053-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,5 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64053-04:
(7*6)+(6*4)+(5*0)+(4*5)+(3*3)+(2*0)+(1*4)=99
99 % 10 = 9
So 64053-04-9 is a valid CAS Registry Number.

64053-04-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-8-methylsulfanyloctane

1.2 Other means of identification

Product number -
Other names 8-Methylthiooctylbromid

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:64053-04-9 SDS

64053-04-9Downstream Products

64053-04-9Relevant academic research and scientific papers

ω-methylsulfanylalkyl glucosinolates: A general synthetic pathway

Mavratzotis, Manolis,Cassel, Stéphanie,Montaut, Sabine,Rollin, Patrick

, (2018/04/09)

A general pathway was devised to synthesize ω-methylsulfanylalkyl glucosinolates, which represent an important class of structurally homogeneous plant secondary metabolites. The required thiofunctionalized hydroximoyl chlorides were obtained from the corresponding α,ω-nitroalkyl methylsulfide precursors, involving as the key-step, a nitronate chlorination strategy. A coupling reaction with 1-thio-beta-D-glucopyranose, followed by O-sulfation of the intermediate thiohydroximate and final deprotection of the sugar moiety afforded the target compounds.

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