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42899-83-2

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42899-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42899-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,8,9 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42899-83:
(7*4)+(6*2)+(5*8)+(4*9)+(3*9)+(2*8)+(1*3)=162
162 % 10 = 2
So 42899-83-2 is a valid CAS Registry Number.

42899-83-2SDS

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 4-chloro-2-phenylisoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 4-chloro-2-phenyl-isoindoline-1,3-dione

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:42899-83-2 SDS

42899-83-2Relevant articles and documents

NOVEL COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

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Paragraph 0389-0392, (2019/10/29)

The present invention relates to a novel compound capable of improving efficiency and low driving voltage and/or lifespan characteristics in an organic light emitting device; and an organic light emitting device including the same. The compound is represe

Unmasking Amides: Ruthenium-Catalyzed Protodecarbonylation of N-Substituted Phthalimide Derivatives

Yuan, Yu-Chao,Kamaraj, Raghu,Bruneau, Christian,Labasque, Thierry,Roisnel, Thierry,Gramage-Doria, Rafael

, p. 6404 - 6407 (2017/12/08)

The unprecedented transformation of a wide range of synthetically appealing phthalimides into amides in a single-step operation has been achieved in high yields and short reaction times using a ruthenium catalyst. Mechanistic studies revealed a unique, homogeneous pathway involving five-membered ring opening and CO2 release with water being the source of protons.

Insecticidal Benzenedicarboxamide Derivative

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Page/Page column 107, (2011/08/06)

The present invention relates to a novel benzenedicarboxamide derivative and the use thereof as an insecticide having the formula (I) wherein the chemical groups W1 to W9, and R1 to R3 are as defined here-in.

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