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[acetoxy-(2-methyl-5-nitrophenyl)methyl] acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72005-83-5

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72005-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72005-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,0 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72005-83:
(7*7)+(6*2)+(5*0)+(4*0)+(3*5)+(2*8)+(1*3)=95
95 % 10 = 5
So 72005-83-5 is a valid CAS Registry Number.

72005-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-5-nitrobenzyliden-diacetat

1.2 Other means of identification

Product number -
Other names -

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:72005-83-5 SDS

72005-83-5Downstream Products

72005-83-5Relevant academic research and scientific papers

ISOQUINOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF DISEASES

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Paragraph 0256; 0280, (2022/02/06)

The present invention discloses compounds according to Formula (I) wherein R1, R2, R3, L1, L2, and L3 are as defined herein. The present invention relates to compounds inhibiting discoidin domain receptors (DDRs), methods for their production, pharmaceutical compositions comprising the same, and methods of treatment using the same, for the prophylaxis and/or treatment of fibrotic diseases, inflammatory diseases, respiratory diseases, autoimmune diseases, metabolic diseases, cardiovascular diseases, and/or proliferative diseases by administering a compound of the invention.

Comparative Reactivity of Substituted 4-Nitrobenzylidene Dichlorides with Alkali

Goh, Swee Hock,Kam, Toh Seok

, p. 423 - 426 (2007/10/02)

A comparative study of the reactions of substituted 4-nitrobenzylidene dichlorides ArCHCl2 (Ar = 3-Cl-4-NO2C6H3, 2-Cl-4-NO2C6H3, 4-NO2C6H4, 3,5-Me2-4-NO2C6H2, and 2-Me-4-NO2C6H3) with aqueous alcoholic alkali shows that chlorine substitution enhances the

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