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acetic acid-(2-isopropenyl-4-nitro-anilide) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

857952-45-5

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857952-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857952-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,9,5 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 857952-45:
(8*8)+(7*5)+(6*7)+(5*9)+(4*5)+(3*2)+(2*4)+(1*5)=225
225 % 10 = 5
So 857952-45-5 is a valid CAS Registry Number.

857952-45-5SDS

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 acetic acid-(2-isopropenyl-4-nitro-anilide)

1.2 Other means of identification

Product number -
Other names Essigsaeure-(4-nitro-2-ispopropenyl-anilid)

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:857952-45-5 SDS

857952-45-5Upstream product

857952-45-5Relevant academic research and scientific papers

Novel synthesis of 2-chloroquinolines from 2-vinylanilines in nitrile solvent

Lee, Byoung Se,Lee, Jae Hak,Chi, Dae Yoon

, p. 7884 - 7886 (2007/10/03)

2-Vinyl- or heteroaryl-substituted anilines were reacted with diphosgene in acetonitrile solution via a reactive imidoyl moiety to afford the corresponding 2-chloroquinolines. Facile syntheses of nine 2-chloroquinoline derivatives from several anilines and their postulate mechanism is described. The postulate mechanism of 2-chloroquinoline formation via imidoyl moiety as a good leaving group shows that the reaction consists of the following three steps: (1) generation of phenylisocyanate, (2) quinoline ring formation, and (3) chlorination on C2 position of quinoline.

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