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5836-66-8

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5836-66-8 Usage

General Description

2,3-Dibromopropylmethyl ether is a chemical compound with the formula C5H10Br2O. It is a colorless liquid with a strong and pungent odor. 2,3-Dibromopropylmethyl ether is mainly used as a chemical intermediate in the synthesis of various organic compounds. It is also used as a solvent and as a reagent in chemical reactions. 2,3-Dibromopropylmethyl ether is known to be a skin and eye irritant and should be handled with care. It is important to use proper protective equipment when handling this chemical to avoid any potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 5836-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5836-66:
(6*5)+(5*8)+(4*3)+(3*6)+(2*6)+(1*6)=118
118 % 10 = 8
So 5836-66-8 is a valid CAS Registry Number.

5836-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dibromo-3-methoxypropane

1.2 Other means of identification

Product number -
Other names 1,2-Dibrom-3-methoxy-propan

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:5836-66-8 SDS

5836-66-8Relevant articles and documents

NaIO4-Mediated Selective Oxidative Halogenation of Alkenes and Aromatics Using Alkali Metal Halides

Dewkar, Gajanan K.,Narina, Srinivasarao V.,Sudalai, Arumugam

, p. 4501 - 4504 (2007/10/03)

(Equation presented) NaIO4 oxidizes alkali metal halides efficiently in aqueous medium to halogenate alkenes and aromatics and produce the corresponding halo derivatives in excellent regio and stereoselectivity. The system also demonstrates the asymmetric version of bromo hydroxylation using β-cyclodextrin complexes, resulting in moderate ee.

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