7510-49-8 Usage
Description
Methyl 2-(benzoylamino)benzoate is a chemical compound with the molecular formula C15H13NO3. It is a valuable ingredient in the pharmaceutical and medical industries, known for its analgesic and anti-inflammatory properties. methyl 2-(benzoylamino)benzoate is also utilized as a precursor for the synthesis of various drugs, particularly for the treatment of diseases such as cancer and inflammation. Furthermore, it serves as an intermediate in organic synthesis for the production of other chemical compounds and has potential applications in materials science for the development of new polymers and coatings.
Uses
Used in Pharmaceutical Industry:
Methyl 2-(benzoylamino)benzoate is used as a precursor for the synthesis of various drugs for the treatment of diseases such as cancer and inflammation. Its analgesic and anti-inflammatory properties make it a valuable ingredient in many medications.
Used in Organic Synthesis:
Methyl 2-(benzoylamino)benzoate is used as an intermediate in organic synthesis for the production of other chemical compounds, contributing to the development of a wide range of products.
Used in Materials Science:
Methyl 2-(benzoylamino)benzoate has potential applications in the field of materials science, where it can be utilized in the development of new polymers and coatings, showcasing its versatility beyond the pharmaceutical domain.
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.
7510-49-8Relevant 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.
