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Benzene, pentabromo(ethoxymethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79415-46-6

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79415-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79415-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,1 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79415-46:
(7*7)+(6*9)+(5*4)+(4*1)+(3*5)+(2*4)+(1*6)=156
156 % 10 = 6
So 79415-46-6 is a valid CAS Registry Number.

79415-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5-pentabromo-6-(ethoxymethyl)benzene

1.2 Other means of identification

Product number -
Other names ethyl pentabromobenzyl ether

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:79415-46-6 SDS

79415-46-6Downstream Products

79415-46-6Relevant academic research and scientific papers

Polybromoaromatic compounds: XI. Reactions of 2,3,4,5,6-pentabromobenzyl bromide with alcohols and alkali metal alkoxides

Shishkin,Vakaeva,Butin

, p. 709 - 712 (2007/10/03)

2,3,4,5,6-Pentabromobenzyl bromide reacts with primary and secondary alcohols and also with alkali metal alkoxides derived from primary alcohols to form the corresponding pentabromobenzyl ethers in high yields. In the reactions with secondary alkoxides, c

Polybromoaromatic compounds: IX. Reactions of polybromobenzyl bromides with enolates derived from some dicarbonyl compounds

Shishkin,Vakaeva,Belozerov,Tanaseichuk,Butin

, p. 975 - 980 (2007/10/03)

The reaction of polybromobenzyl bromides RC6Br4CH2Br (R = Br, OCH3) with diethyl malonate sodium salt in ethanol and dimethylformamide leads to formation of diethyl 2-(polybromobenzyl)malonates, whereas in aqueous ethanol ethyl polybromobenzyl malonates are formed. The same polybromobenzyl bromides react with an equimolar amount of ethyl acetoacetate sodium salt or acetylacetone sodium salt to give C-alkylation products; with excess sodium enolates ethyl 3-(polybromophenyl)propionates and 4-(polybromophenyl)-2-butanones are formed, respectively.

POLYBROMO AROMATIC COMPOUNDS. I. SYNTHESIS OF SOME DERIVATIVES CONTAINING A PENTABROMOPHENYL RESIDUE

Tanaseichuk, B. S.,Rumyantseva, K. S.,Vasin, V. A.,Shishkin, V. N.,Rumyantsev, N. P.,et al.

, p. 1124 - 1128 (2007/10/02)

The synthesis of pentabromobenzyl bromide has been carried out, and its nucleophilic substitution reactions with alcohols, amines, sodium acetate, and silver nitrite have been studied.The C-Br bond in the bromomethyl group of pentabromobenzyl bromide readily undergoes homolysis, resulting in reductive dehalogenation.

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