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Benzoic acid, 3-amino-5-chloro-2-methyl-, methyl ester is a chemical compound with the molecular formula C9H10ClNO2. It is an ester derivative of benzoic acid, characterized by the presence of an amino group, a chloro substituent, and a methyl group on the benzene ring. Benzoic acid, 3-aMino-5-chloro-2-Methyl-, Methyl ester is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its versatile chemical properties.

294190-18-4

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294190-18-4 Usage

Uses

Used in Pharmaceutical Industry:
Benzoic acid, 3-amino-5-chloro-2-methyl-, methyl ester is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be chemically modified and incorporated into drug molecules. Its antimicrobial and antifungal properties also make it a potential candidate for the development of new antimicrobial agents to combat drug-resistant infections.
Used in Agrochemical Industry:
In the agrochemical industry, Benzoic acid, 3-amino-5-chloro-2-methyl-, methyl ester is utilized as an intermediate in the production of pesticides and other agrochemicals. Its antimicrobial properties can be harnessed to develop new compounds that protect crops from diseases and pests, thereby increasing agricultural productivity.
Used in Industrial Applications:
Benzoic acid, 3-amino-5-chloro-2-methyl-, methyl ester can be used in various industrial applications, such as in the manufacturing of plastics, resins, and other polymers. Its chemical properties allow it to be incorporated into these materials to enhance their performance characteristics, such as durability, stability, and resistance to microbial degradation.
It is important to handle Benzoic acid, 3-amino-5-chloro-2-methyl-, methyl ester with care, as it may have potential hazards if not used properly. Proper safety measures should be taken during its synthesis, storage, and application to minimize any risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 294190-18-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,4,1,9 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 294190-18:
(8*2)+(7*9)+(6*4)+(5*1)+(4*9)+(3*0)+(2*1)+(1*8)=154
154 % 10 = 4
So 294190-18-4 is a valid CAS Registry Number.

294190-18-4SDS

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 Methyl 3-amino-5-chloro-2-methylbenzoate

1.2 Other means of identification

Product number -
Other names methyl3-amino-5-chloro-2-methylbenzoate

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:294190-18-4 SDS

294190-18-4Relevant academic research and scientific papers

The Importance of Being Me: Magic Methyls, Methyltransferase Inhibitors, and the Discovery of Tazemetostat

Kuntz, Kevin W.,Campbell, John E.,Keilhack, Heike,Pollock, Roy M.,Knutson, Sarah K.,Porter-Scott, Margaret,Richon, Victoria M.,Sneeringer, Chris J.,Wigle, Tim J.,Allain, Christina J.,Majer, Christina R.,Moyer, Mikel P.,Copeland, Robert A.,Chesworth, Richard

supporting information, p. 1556 - 1564 (2016/03/05)

Posttranslational methylation of histones plays a critical role in gene regulation. Misregulation of histone methylation can lead to oncogenic transformation. Enhancer of Zeste homologue 2 (EZH2) methylates histone 3 at lysine 27 (H3K27) and abnormal methylation of this site is found in many cancers. Tazemetostat, an EHZ2 inhibitor in clinical development, has shown activity in both preclinical models of cancer as well as in patients with lymphoma or INI1-deficient solid tumors. Herein we report the structure-activity relationships from identification of an initial hit in a high-throughput screen through selection of tazemetostat for clinical development. The importance of several methyl groups to the potency of the inhibitors is highlighted as well as the importance of balancing pharmacokinetic properties with potency.

ENHANCER OF ZESTE HOMOLOG 2 INHIBITORS

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Page/Page column 108; 109, (2013/12/03)

This invention relates to novel substituted benzamide according to Formula (I) which are inhibitors of Enhancer of Zeste Homolog 2 (EZH2), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy for the treatment of cancers.

SUBSTITUTED BENZENE COMPOUNDS

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Page/Page column 264-265, (2012/11/06)

The present invention relates to substituted benzene compounds. The present invention also relates to pharmaceutical compositions containing these compounds and methods of treating cancer by administering these compounds and pharmaceutical compositions to subjects in need thereof. The present invention also relates to the use of such compounds for research or other non-therapeutic purposes.

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