53663-39-1 Usage
Description
2-Bromo-3-methylbenzoic acid is an organic compound with the molecular formula C8H7BrO2. It is an off-white powder and serves as an important intermediate in the synthesis of various organic compounds.
Uses
Used in Pharmaceutical Industry:
2-Bromo-3-methylbenzoic acid is used as a synthetic intermediate for the production of N-phenyl-3-methylanthranilic acid, which is achieved through a copper-catalyzed amination reaction with aniline. This synthesized compound has potential applications in the development of pharmaceuticals.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-Bromo-3-methylbenzoic acid is utilized as a key intermediate in the preparation of various organic compounds, contributing to the diversity of chemical products and their applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 53663-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,6 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53663-39:
(7*5)+(6*3)+(5*6)+(4*6)+(3*3)+(2*3)+(1*9)=131
131 % 10 = 1
So 53663-39-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrO2/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4H,1H3,(H,10,11)
53663-39-1Relevant articles and documents
METHOD FOR PRODUCING TETRAZOLINONE COMPOUND
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Paragraph 0142; 0143, (2017/03/21)
A tetrazolinone compound represented by formula (1): [in the formula, R1 represents an alkyl group having 1-6 carbon atoms or the like] can be produced by reacting a compound represented by formula (2): [in the formula, X1 represents
Selective Oxidation of 2-Bromo-m-xylene to 2-Bromo-3-methylbenzoic Acid or 2-Bromoisophthalic Acid
Miyano, Sotaro,Fukushima, Hiroshi,Inagawa, Hideho,Hashimoto, Harukichi
, p. 3285 - 3286 (2007/10/02)
Aqueous sodium dichromate oxidation of 2-bromo-m-xylene (1) under a carbon dioxide pressure gave 2-bromoisophthalic acid (58percent), while NBS-bromination of 1 followed by Sommelet oxidation to aldehyde and then potassium permanganate oxidation enabled t
