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Benzene, 1-(1,1-dimethylethyl)-4-(tribromomethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75485-49-3

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75485-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75485-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,8 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75485-49:
(7*7)+(6*5)+(5*4)+(4*8)+(3*5)+(2*4)+(1*9)=163
163 % 10 = 3
So 75485-49-3 is a valid CAS Registry Number.

75485-49-3SDS

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-tert-butyl-4-(tribromomethyl)benzene

1.2 Other means of identification

Product number -
Other names p-tert.butylbenzotribromide

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:75485-49-3 SDS

75485-49-3Upstream product

75485-49-3Downstream Products

75485-49-3Relevant academic research and scientific papers

Preparation method of diaryl acetylene compounds

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Paragraph 0057; 0058; 0059; 0070, (2018/05/16)

The invention relates to preparation of an organic compound, and aims to provide a preparation method of diaryl acetylene compounds. The preparation method includes steps of adding associated tribromomethylarene compound and copper in a reactor to perform deoxidizing treatment; dissolving polyamine in a proper amount of anhydrous and oxygen-free solvent, and then adding to the reactor; performingcoupling reaction at 30-80DEG C for 3-12 hours; separating and purifying to obtain diaryl acetylene compounds. The preparation is gentle in synthesis condition and the reaction has good compatibilityto different functional groups; the raw material associated tribromomethylarene compound is convenient to compound and has different substituent groups and variable structure; by adopting one raw material, high-quality product can be obtained through simple treatment, and the output is high; by adopting two different raw materials, the asymmetrical diaryl acetylene compound can be prepared.

P-Tert.butylbenzotribromide and p-tert.butylbenzoyl bromide and process for their manufacture

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, (2008/06/13)

p-Tert.butylbenzotribromide and the derivatives thereof which is halogen-substituted at the nucleus are prepared under side chain halogenation conditions by bromination of p-tert.butyltoluene and its derivatives substituted at the nucleus by halogen. Prac

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