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Benzoic acid, 3-amino-4,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

348165-23-1

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348165-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 348165-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,8,1,6 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 348165-23:
(8*3)+(7*4)+(6*8)+(5*1)+(4*6)+(3*5)+(2*2)+(1*3)=151
151 % 10 = 1
So 348165-23-1 is a valid CAS Registry Number.

348165-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-4,5-dimethylbenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,3-amino-4,5-dimethyl

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:348165-23-1 SDS

348165-23-1Upstream product

348165-23-1Downstream Products

348165-23-1Relevant academic research and scientific papers

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

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

, p. 825 - 828 (2002)

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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