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88975-09-1

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88975-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88975-09-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,7 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88975-09:
(7*8)+(6*8)+(5*9)+(4*7)+(3*5)+(2*0)+(1*9)=201
201 % 10 = 1
So 88975-09-1 is a valid CAS Registry Number.

88975-09-1SDS

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 diethyl 2-[(2-chloro-4-nitrophenyl)methyl]propanedioate

1.2 Other means of identification

Product number -
Other names Propanedioic acid,(2-chloro-4-nitrophenyl)methyl-,diethyl ester

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:88975-09-1 SDS

88975-09-1Relevant articles and documents

Bis(dealkoxycarbonylation) of nitroarylmalonates: A facile entry to alkylated nitroaromatics

Gurjar,Reddy,Murugaiah,Murugaiah

, p. 1659 - 1661 (2007/10/03)

A simple approach to alkylated nitroaromatics from substituted nitroaryl malonic esters by double decarboxylation is detailed.

Nonsteroidal antiinflammatory agents. 2. [(Heteroarylamino)phenyl]alkanoic acids

Hino,Nakamura,Nagai,Uno,Nishimura

, p. 222 - 226 (2007/10/02)

A series of [(heteroarylamino)phenyl]alkanoic acids pyridine, quinoline, or pyrimidine as the heteroaryl moiety was prepared as potential antiinflammatory agents. Among them, 2-[4-(2-pyridylamino)phenyl]propionic acid (14b) showed excellent antiinflammatory and analgesic activities with less tendency to cause gastric side effects. Structure-activity relationships are discussed.

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