253120-47-7 Usage
Uses
Used in Flavor and Fragrance Industry:
METHYL 2-AMINO-3-CARBOXYBENZOATE is used as a flavoring agent for its distinctive fruity, grape-like aroma, adding a natural scent to foods, beverages, and perfumes, enhancing the sensory experience of consumers.
Used in Insect Repellent Production:
METHYL 2-AMINO-3-CARBOXYBENZOATE is used as an active ingredient in insect repellents, leveraging its natural properties to deter insects, offering an alternative to synthetic repellents.
Used in Natural Pesticide Development:
METHYL 2-AMINO-3-CARBOXYBENZOATE is used as a potential natural pesticide, being studied for its ability to control pests in an environmentally friendly manner, reducing the reliance on chemical pesticides.
Used in Medicinal Research:
METHYL 2-AMINO-3-CARBOXYBENZOATE is used as a subject of medicinal research for its potential anti-inflammatory and antimicrobial properties, exploring its therapeutic applications in treating various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 253120-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,1,2 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 253120-47:
(8*2)+(7*5)+(6*3)+(5*1)+(4*2)+(3*0)+(2*4)+(1*7)=97
97 % 10 = 7
So 253120-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO4/c1-14-9(13)6-4-2-3-5(7(6)10)8(11)12/h2-4H,10H2,1H3,(H,11,12)
253120-47-7Relevant academic research and scientific papers
QUINAZOLINE DERIVATIVES AS ANTIVIRAL AGENTS
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Page/Page column 31, (2010/11/26)
The present invention relates to the use of quinazoline derivatives of formula (I) wherein A, B, R1, R2, R3 and R4 are defined herein, and pharmaceutically acceptable salts thereof, for the treatment or preventi
A preparation of methyl 2-amino-3-formylbenzoate and its use in Friedlander synthesis
Bu, Xianyong,Deady, Leslie W.
, p. 4223 - 4233 (2007/10/03)
The title compound has been prepared in four steps from methyl isatin-7- carboxylate. Condensations with 1-indanone and analogs gave 11H-indeno[1,2- b]quinoline-6-carboxylic acids, and with cyclohexanones gave acridine-4- carboxylic acids.
