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24308-78-9

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24308-78-9 Usage

Structure

A benzene ring with two bromine atoms and an ethyl group attached via a bromo substituent

Derivative

Benzene

Functional groups

Bromine atoms, ethyl group

Uses

Intermediate in the synthesis of various organic compounds, building block for pharmaceuticals, agrochemicals, and dyes, potential applications in materials science and advanced polymers

Safety precautions

Handled and stored with proper safety due to its toxic and corrosive nature

Check Digit Verification of cas no

The CAS Registry Mumber 24308-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,0 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24308-78:
(7*2)+(6*4)+(5*3)+(4*0)+(3*8)+(2*7)+(1*8)=99
99 % 10 = 9
So 24308-78-9 is a valid CAS Registry Number.

24308-78-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-(1-bromoethyl)benzene

1.2 Other means of identification

Product number -
Other names (+)-1-(4'-bromophenyl)bromoethane

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:24308-78-9 SDS

24308-78-9Relevant articles and documents

Preparation of chiral 1-phenylethanols and bromides

Stein, Allan R.,Dawe, Robert D.,Sweet, James R.

, p. 3442 - 3448 (2007/10/02)

A fast, convenient procedure for preparing and resolving moderate to large quantities of chiral secondary alcohols is described.The general procedure involves a one-pot conversion of the ketone (various acetophenones) to the half-ester of a diacid (succinic, phthalic...) and resolution with (+)- and (-)-1-phenylethylamines.Overall yields of the enantiomeric alcohols, the variously substituted 1-phenylethanols, are generally 65-85percent with optical purities of approximately 90percent.Properties and optical rotations of a number of chiral 1-phenylethanols and of the bromides made from them are tabulated.A discussion of optical purity determinations using nmr methods is included and absolute configurations are reported.

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