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74319-96-3

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74319-96-3 Usage

General Description

3,4-Dimethyl-5-nitro-benzoic acid is a compound with the chemical formula C9H9NO4. It is a yellow crystalline powder that is used in the pharmaceutical industry as an intermediate for the synthesis of various organic compounds. This chemical is known for its nitro and carboxylic acid groups, which make it useful in the development of drugs and other pharmaceutical products. It has also been studied for its potential antimicrobial and antioxidant properties, making it a versatile and important chemical in various fields of research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 74319-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,1 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74319-96:
(7*7)+(6*4)+(5*3)+(4*1)+(3*9)+(2*9)+(1*6)=143
143 % 10 = 3
So 74319-96-3 is a valid CAS Registry Number.

74319-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-Dimethyl-5-nitrobenzoesaeure

1.2 Other means of identification

Product number -
Other names 3-nitro-4,5-dimethyl benzoic acid

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:74319-96-3 SDS

74319-96-3Relevant articles and documents

An improved synthesis of 5,6-dimethylxanthenone-4-acetic acid (DMXAA)

Atwell, Graham J,Yang, Shangjin,Denny, William A

, p. 825 - 828 (2007/10/03)

5,6-Dimethylxanthenone-4-acetic acid (DMXAA) is a novel anticancer agent with a number of unique activities, and is in clinical trial. The current synthesis of DMXAA involves six steps, beginning with a heterogeneous reaction to form an isonitrosoacetanilide, and gives an overall yield of 11% from 2,3-dimethylaniline. We report an alternative synthesis of the key intermediate 3,4-dimethylanthranilic acid via nitration of 3,4-dimethylbenzoic acid and separation of the key desired isomer by ready crystallisation. This, together with improvements in the rest of the synthesis, provide a shorter and higher-yielding route to DMXAA (22% overall from 3,4-dimethylbenzoic acid).

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