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7510-49-8

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7510-49-8 Usage

General Description

Methyl 2-(benzoylamino)benzoate is a chemical compound with the molecular formula C15H13NO3. It is commonly used in the pharmaceutical and medical industries as a precursor for the synthesis of various drugs, particularly for the treatment of diseases such as cancer and inflammation. It is also used as an intermediate in organic synthesis for the production of other chemical compounds. Methyl 2-(benzoylamino)benzoate is known for its analgesic and anti-inflammatory properties, making it a valuable ingredient in many medications. Additionally, it has potential applications in the field of materials science for the development of new polymers and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 7510-49-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7510-49:
(6*7)+(5*5)+(4*1)+(3*0)+(2*4)+(1*9)=88
88 % 10 = 8
So 7510-49-8 is a valid CAS Registry Number.

7510-49-8SDS

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-benzamidobenzoate

1.2 Other means of identification

Product number -
Other names N-Benzoyl-anthranilsaeure-methylester

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:7510-49-8 SDS

7510-49-8Relevant articles and documents

Synthesis, structural characterization and biological evaluation of mononuclear transition metal complexes of zwitterionic dehydroacetic acid N-aroylhydrazone ligand

Kendur, Umashri,Chimmalagi, Geeta H.,Patil, Sunil M.,Gudasi, Kalagouda B.,Frampton, Christopher S.

, (2018)

Synthesis and characterization of mononuclear transition metal complexes viz., Co(II), Ni(II), Cu(II) and Zn(II) with a newly designed ligand, (E)-2-benzamido-N'-(1-(2-hydroxy-6-methyl-4-oxo-4H-pyran-3-yl) ethylidene) benzohydrazide (H2L) are r

Asymmetric Synthesis of N-N Axially Chiral Compounds by Phase-Transfer-Catalyzed Alkylations

Pan, Ming,Shao, Ying-Bo,Zhao, Qun,Li, Xin

supporting information, p. 374 - 378 (2022/01/04)

N-N axially chiral skeletons are significant structural motifs in natural products, pharmaceuticals, and functional materials. Herein we disclose a method for the asymmetric synthesis of N-N axially chiral compounds by phase-transfer catalysis. A wide range of N-N axially chiral quinazolinone derivatives were prepared in high yields with excellent stereoselectivities. Furthermore, the synthetic utility of the protocol was proved by large-scale reaction and transformation of the product. Density functional theory calculations provide insight into the mechanism.

Tunable Electrosynthesis of Anthranilic Acid Derivatives via a C-C Bond Cleavage of Isatins

Qian, Peng,Liu, Jiaojiao,Zhang, Yan,Wang, Zhiyong

, p. 16008 - 16015 (2021/07/31)

A facile and direct electrocatalytic C-C bond cleavage/functionalization reaction of isatins was developed. With isatins as the amino-attached C1 sources, a variety of aminobenzoates, and aminobenzamides were synthesized in moderate to good yields under mild conditions.

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