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64141-90-8

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64141-90-8 Usage

General Description

2-BROMO-N-ISOPROPYLBENZAMIDE is a chemical compound that belongs to the class of organic compounds known as benzamides. It is a white crystalline solid that is soluble in organic solvents such as ethanol and methanol. This chemical is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been found to have potential applications in the field of medicinal chemistry as an anti-inflammatory and analgesic agent. Additionally, it is a useful building block in organic synthesis for the preparation of various heterocyclic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 64141-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,4 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64141-90:
(7*6)+(6*4)+(5*1)+(4*4)+(3*1)+(2*9)+(1*0)=108
108 % 10 = 8
So 64141-90-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12BrNO/c1-7(2)12-10(13)8-5-3-4-6-9(8)11/h3-7H,1-2H3,(H,12,13)

64141-90-8SDS

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 2-bromo-N-propan-2-ylbenzamide

1.2 Other means of identification

Product number -
Other names 2-Bromo-N-isopropylbenzamide

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:64141-90-8 SDS

64141-90-8Downstream Products

64141-90-8Relevant articles and documents

Tailoring buchwald-type phosphines with pyrimidinium betaines as versatile aryl group surrogates

Nol-Duchesneau, Ludovik,Lugan, Nol,Lavigne, Guy,Labande, Agns,Csar, Vincent

supporting information, p. 5085 - 5088 (2014/12/11)

A derivatization of dialkylbiarylphosphines consisting in the formal replacement of their distal aryl group by a pyrimidinium betaine is reported. Two achiral representatives of this new class of Buchwald-type phosphines have been successfully synthesized through two strategies. The first one is based on a last stage introduction of the phosphino moiety, and the second one consists in a modular, one-pot, three-step procedure starting from an o-bromoaryl phosphine. The resulting phosphines have been coordinated onto gold(I) and palladium(II) centers and have been employed as supporting ligands in Pd-catalyzed Suzuki-Miyaura cross-coupling of aryl halide substrates.

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