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54462-70-3

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54462-70-3 Usage

Physical state

Colorless liquid

Uses

Intermediate in the synthesis of various organic compounds

Chemical structure

Butane backbone with two methyl groups (-CH3) and two bromine atoms (Br) attached at specific carbon positions

Reactivity

Presence of bromine atoms makes it reactive and useful in organic synthesis

Applications

Production of pharmaceuticals, agrochemicals, and other specialty chemicals

Additional uses

Solvent or reagent in chemical reactions

Safety precautions

Toxic and may cause skin and eye irritation; handle with caution

Check Digit Verification of cas no

The CAS Registry Mumber 54462-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,6 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54462-70:
(7*5)+(6*4)+(5*4)+(4*6)+(3*2)+(2*7)+(1*0)=123
123 % 10 = 3
So 54462-70-3 is a valid CAS Registry Number.

54462-70-3SDS

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 1,4-dibromo-2,3-dimethylbutane

1.2 Other means of identification

Product number -
Other names Butane, 1,4-dibromo-2,3-dimethyl-

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:54462-70-3 SDS

54462-70-3Downstream Products

54462-70-3Relevant articles and documents

Selective Skeletal Rearrangement by Carbon-Carbon Bond Activation

Takahashi, Tamotsu,Fujimori, Takayasu,Seki, Takashi,Saburi, Masahiko,Uchida, Yasuzo,et al.

, p. 182 - 183 (1990)

Skeletal rearrangement of α-substituted organometallic compounds to give β-substituted compounds by carbon-carbon bond activation was performed with bis(η5-cyclopentadienyl)-2,5-dimethyl-zircona- or -hafna-cyclopentane, which were regio- and stereo-selectively converted into the corresponding 3,4-dimethylmetallacyclopentanes in high yields.

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