5363-30-4 Usage
Uses
Used in Pharmaceutical Research and Development:
2-[(2-chlorobenzyl)amino]benzoic acid is used as a compound of interest for its potential biological activity, which makes it a candidate for pharmaceutical research and development. Its complex structure with a benzene ring and a carboxylic acid group may contribute to its interactions with biological systems, offering opportunities for the creation of new therapeutic agents.
Used in Chemical Synthesis:
In the chemical industry, 2-[(2-chlorobenzyl)amino]benzoic acid may be used as a building block or intermediate in the synthesis of more complex molecules. Its unique structure with a chlorobenzyl group and a carboxylic acid group can be exploited in the creation of novel compounds with specific properties and applications.
Used in Material Science:
2-[(2-chlorobenzyl)amino]benzoic acid could also find applications in material science, where its chemical structure might be utilized to develop new materials with tailored properties. The presence of a carboxylic acid group and a chlorobenzyl group could enable the compound to form part of polymers or other materials with specific characteristics, such as improved stability or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 5363-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5363-30:
(6*5)+(5*3)+(4*6)+(3*3)+(2*3)+(1*0)=84
84 % 10 = 4
So 5363-30-4 is a valid CAS Registry Number.
5363-30-4Relevant academic research and scientific papers
Copper catalyzed C-N bond formation/C-H activation: Synthesis of aryl 4H-3,1-benzoxazin-4-ones
Munusamy, Sathishkumar,Venkatesan, Sathesh,Sathiyanarayanan, Kulathu Iyer
supporting information, p. 203 - 205 (2015/02/02)
We have developed a practical and efficient synthesis of 2-phenyl-4H-benzo[d][1,3]oxazine-4-one derivatives through copper catalyzed tandem reaction of 2-iodobenzoic acid with arylmethanamines under aerobic conditions. Compared to the literature methods toward the synthesis of 2-phenyl-4H-benzo[d][1,3]oxazine-4-one, the synthetic method reported in this Letter has broad substrate scope, mild reaction condition, and uses an inexpensive catalyst.
