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1254319-51-1

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1254319-51-1 Usage

General Description

1H-Isoindol-1-one, 6-bromo-2,3-dihydro-2-Methyl- is a chemical compound belonging to the subgroup of Isoindolines. It has a bromine substituent at position 6, a methyl group at position 2, and the 2,3-dihydroxy configuration on the isoindolone ring system. This chemical is often used in research and development for the manufacturing of a variety of products and in other chemical reactions. However, its physical properties like melting point, boiling point, density, and specific rotation, as well as safety information, could vary depending on different factors such as preparation methods and purity. Like many other chemicals, it should be handled and stored properly to ensure safety and effectiveness.

Check Digit Verification of cas no

The CAS Registry Mumber 1254319-51-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,3,1 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1254319-51:
(9*1)+(8*2)+(7*5)+(6*4)+(5*3)+(4*1)+(3*9)+(2*5)+(1*1)=141
141 % 10 = 1
So 1254319-51-1 is a valid CAS Registry Number.

1254319-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-2-methyl-3H-isoindol-1-one

1.2 Other means of identification

Product number -
Other names 6-bromo-2-methyl-2,3-dihydro-1H-isoindol-1-one

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:1254319-51-1 SDS

1254319-51-1Relevant articles and documents

Smooth isoindolinone formation from isopropyl carbamates via bischler-napieralski-type cyclization

Adachi, Satoshi,Onozuka, Masao,Yoshida, Yuko,Ide, Mitsuaki,Saikawa, Yoko,Nakata, Masaya

, p. 358 - 361 (2014/04/03)

Isopropyl carbamates derived from benzylamines provide isoindolinones by treatment with phosphorus pentoxide at room temperature. Utility of this Bischler-Napieralski-type cyclization and a new mechanism involving a carbamoyl cation for rationalization of this smooth conversion are discussed.

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