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2-Chloro-3-methylbenzoic acid methyl ester is a chemical compound with the molecular formula C9H9ClO2. It is an ester derivative of 2-chloro-3-methylbenzoic acid, characterized by its white solid appearance and a molecular weight of 184.62 g/mol. With a melting point of approximately 75-78°C, this versatile building block is widely utilized in organic synthesis, chemical research, and the production of pharmaceuticals, agrochemicals, and other fine chemicals.

920759-93-9

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920759-93-9 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-3-methylbenzoic acid methyl ester is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-3-methylbenzoic acid methyl ester serves as a crucial component in the production of pesticides and other crop protection agents. Its incorporation enhances the effectiveness of these products, contributing to improved agricultural yields.
Used in Organic Synthesis:
As a versatile building block, 2-Chloro-3-methylbenzoic acid methyl ester is used in organic synthesis for the creation of a wide range of organic compounds. Its reactivity and functional groups make it a valuable precursor in the synthesis of various chemical entities.
Used in Chemical Research:
In the field of chemical research, 2-Chloro-3-methylbenzoic acid methyl ester is employed as a model compound to study various chemical reactions and mechanisms. Its properties provide insights into the behavior of similar ester derivatives and contribute to the advancement of chemical knowledge.

Check Digit Verification of cas no

The CAS Registry Mumber 920759-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,0,7,5 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 920759-93:
(8*9)+(7*2)+(6*0)+(5*7)+(4*5)+(3*9)+(2*9)+(1*3)=189
189 % 10 = 9
So 920759-93-9 is a valid CAS Registry Number.

920759-93-9SDS

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 methyl 2-chloro-3-methylbenzoate

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:920759-93-9 SDS

920759-93-9Relevant academic research and scientific papers

NITROGEN-CONTAINING HETEROCYCLIC COMPOUND AND COMPOSITION THEREOF, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF

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Paragraph 0308-0309, (2021/10/07)

Disclosed by the present invention are a nitrogen-containing heterocyclic compound, and a composition thereof, a preparation method therefor and an application thereof. The structure of the nitrogen-containing heterocyclic compound according to the presen

HETEROCYCLIC COMPOUND AND USE THEREOF

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Page/Page column 97, (2010/06/11)

Disclosed is a heterocyclic compound having a strong Raf inhibitory activity. Specifically disclosed is a compound represented by the formula (I), (II) or (III) below, or a salt thereof. (In the formulae, the symbols are as defined in the description.)

Design, synthesis and identification of novel colchicine-derived immunosuppressant

Chang, Dong-Jo,Yoon, Eun-Young,Lee, Geon-Bong,Kim, Soon-Ok,Kim, Wan-Joo,Kim, Young-Myeong,Jung, Jong-Wha,An, Hongchan,Suh, Young-Ger

scheme or table, p. 4416 - 4420 (2010/04/05)

Synthesis and biological evaluation of various colchicine analogues through the mixed-lymphocyte reaction (MLR), lymphoproliferation, and inhibitory effects on the inflammatory genes are described. In addition, a new series of immunosuppressive agents developed on the structural basis of colchicine, as well as their structure-activity relationships is reported. The most potent analogue 20a exhibited an excellent immunosuppressive activity on in vivo skin-allograft model, which is comparable to that of cyclosporin A.

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