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1222-42-0

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1222-42-0 Usage

General Description

2-[(2,3-Dimethylphenyl)amino]benzoic acid methyl ester is a chemical compound that is derived from benzoic acid and contains a methyl ester group. It is also known as methyl 2-[(2,3-dimethylphenyl)amino]benzoate. 2-[(2,3-Dimethylphenyl)amino]benzoic acid methyl ester is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various organic compounds. It has potential applications in the production of medicines and drugs, as well as in research and development. The presence of the dimethylphenylamino group makes this compound a useful building block for the synthesis of a wide range of compounds with diverse properties and applications. Its chemical structure and properties make it an important and versatile compound in various chemical and pharmaceutical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1222-42-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1222-42:
(6*1)+(5*2)+(4*2)+(3*2)+(2*4)+(1*2)=40
40 % 10 = 0
So 1222-42-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H17NO2/c1-11-7-6-10-14(12(11)2)17-15-9-5-4-8-13(15)16(18)19-3/h4-10,17H,1-3H3

1222-42-0SDS

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 2-(2,3-dimethylanilino)benzoate

1.2 Other means of identification

Product number -
Other names 2-[(2,3-Dimethylphenyl)amino]benzoic acid,methyl ester

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:1222-42-0 SDS

1222-42-0Relevant articles and documents

Synthesis and evaluation of some new hydrazones as corrosion inhibitors for mild steel in acidic media

Lgaz, Hassane,Chaouiki, Abdelkarim,Albayati, Mustafa R.,Salghi, Rachid,El Aoufir, Yasmina,Ali, Ismat H.,Khan, Mohammad I.,Mohamed, Shaaban K.,Chung, Ill-Min

, p. 2269 - 2286 (2019)

Mild steel corrosion in HCl solution is an example of corrosion in acidic mediums. The ongoing research efforts to develop novel environmentally friendly corrosion inhibitors raise questions regarding their ability to effectively protect steel from corros

Synthesis, experimental and theoretical characterization of (E)-2-((2,3-dimethylphenyl)amino)-N’-(furan-2-ylmethylene)benzohydrazide

Albayati, Mustafa R.,Ali, Ismat H.,Chung, Ill-Min,Dege, Necmi,Kans?z, Sevgi,Kaya, Sava?,Lgaz, Hassane,Salghi, Rachid

, (2020)

Hydrazone derivatives have drawn much attention because of their large pharmacological applications. In the present work, the compound (E)-2-((2,3-dimethylphenyl)amino)-N’-(furan-2-ylmethylene)benzohydrazide, noted C20H19N3/sub

Synthesis, analgesic and anti-inflammatory activities of chalconyl-incorporated hydrazone derivatives of mefenamic acid

Kumar, Neeraj,Chauhan, Lalit Singh,Sharma, Chandra Shekhar,Dashora, Nipun,Bera, Rajendra

, p. 2580 - 2590 (2015/02/05)

A series of chalconyl-incorporated hydrazone derivatives of mefenamic acid was synthesized in order to obtain new compounds with potential analgesic and anti-inflammatory activity having lesser side effects. The structures of all synthesized compounds were confirmed by means of elemental analysis, IR, 1H NMR, 13C NMR and mass spectra. All compounds were evaluated for their analgesic and anti-inflammatory activities by tail-flick method and carrageenan-induced rat paw edema test, respectively. Among all the synthesized compounds, compounds (4a) and (4j) exhibited the most prominent and consistent anti-inflammatory activity. In acute ulcerogenicity study, it can be concluded that compounds (4a) and (4j) are devoid of the deadlier gastrointestinal toxicities.

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