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850012-44-1

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850012-44-1 Usage

Uses

4-Bromo-2-tert-butylaniline is an intermediate in the synthesis of 1-(2-tert-Butyl-4-bromophenyl)pyrrolidin-2-one (T135885), which is an intermediate in the preparation of [1,1'':3'',1'''']terphenyl-4-carboxylic acid and esters as ligands modulating retinoic acid receptors (RAR).

Check Digit Verification of cas no

The CAS Registry Mumber 850012-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,0,1 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 850012-44:
(8*8)+(7*5)+(6*0)+(5*0)+(4*1)+(3*2)+(2*4)+(1*4)=121
121 % 10 = 1
So 850012-44-1 is a valid CAS Registry Number.

850012-44-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-2-tert-butylaniline

1.2 Other means of identification

Product number -
Other names 4-bromo-2-tert-butylphenylamine

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:850012-44-1 SDS

850012-44-1Relevant articles and documents

New method for the synthesis of N-tert-alkoxyarylaminyl radicals

Miura, Yozo,Muranaka, Yoshikazu,Teki, Yoshio

, p. 4786 - 4794 (2006)

The reactions of 2,4-diaryl-6-tert-butylnitrosobenzenes with 2,2′-azobis[2-(methoxycarbonyl)propane] (5a), 2,2′-azobis(2-cyano-4- methylpentane) (5b), and 2,2′-azobis(2-cyano-4-methyl-4-methoxypentane) (5c) in refluxing benzene gave stable N-tert-alkoxy-2

KRAS G12C INHIBITORS AND METHODS OF USING THE SAME

-

Paragraph 0255; 0256, (2019/11/22)

Provided herein are KRAS G12C inhibitors, composition of the same, and methods of using the same. These inhibitors are useful for treating a number of disorders, including pancreatic, colorectal, and lung cancers.

Iron-Catalyzed Intramolecular Aminations of C(sp3)?H Bonds in Alkylaryl Azides

Alt, Isabel T.,Guttroff, Claudia,Plietker, Bernd

supporting information, p. 10582 - 10586 (2017/08/22)

The nucleophilic iron complex Bu4N[Fe(CO)3(NO)] (TBA[Fe]) catalyzes the direct intramolecular amination of unactivated C(sp3)?H bonds in alkylaryl azides, which results in the formation of substituted indoline and tetrahydroquinoline derivatives.

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