21702-79-4 Usage
Description
METHYL 3,5-DIBROMO-2-HYDROXYBENZOATE is a white crystalline powder that is a derivative of benzoic acid with two bromine atoms and a hydroxyl group. It is a halogenated aromatic compound that is synthesized through the halogenation of phenol derivatives.
Uses
Used in Chemical Synthesis:
METHYL 3,5-DIBROMO-2-HYDROXYBENZOATE is used as an intermediate in the preparation of Haloarenes, which are important compounds in the chemical industry. These Haloarenes have a wide range of applications, including pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
METHYL 3,5-DIBROMO-2-HYDROXYBENZOATE is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, METHYL 3,5-DIBROMO-2-HYDROXYBENZOATE is used as a starting material for the synthesis of various pesticides and other agrochemical products. Its halogenated structure contributes to the development of more effective and targeted pest control agents.
Used in Materials Science:
METHYL 3,5-DIBROMO-2-HYDROXYBENZOATE is also used in the development of new materials with specific properties, such as flame retardants, polymer additives, and specialty coatings. Its chemical structure provides unique characteristics that can enhance the performance of these materials.
Check Digit Verification of cas no
The CAS Registry Mumber 21702-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,0 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21702-79:
(7*2)+(6*1)+(5*7)+(4*0)+(3*2)+(2*7)+(1*9)=84
84 % 10 = 4
So 21702-79-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H6Br2O3/c1-13-8(12)5-2-4(9)3-6(10)7(5)11/h2-3,11H,1H3
21702-79-4Relevant articles and documents
Monoamine oxidase and succinate dehydrogenase inhibitory properties of substituted 1,3,4-oxadiazole-2-thiones
Soni,Barthwal,Saxena,et al.
, p. 29 - 32 (1982)
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Enantioselective bromolactonization of conjugated (2)-enynes
Zhang, Wei,Zheng, Suqing,Liu, Na,Werness, Jenny B.,Guzei, Llia A.,Tang, Weiplng
supporting information; experimental part, p. 3664 - 3665 (2010/05/15)
"Chemical equation presented" A catalytic enantioselective syn-1,4-bromolactonization of conjugated (Z)-enynes was reported. Diastereomeric ratios >20:1 and up to 99% enantiomeric excesses were observed. Di-, tri-, and tetra-substituted bromoallenes were prepared together with lactone heterocycles efficiently and stereoselectively. Preliminary investigations suggest that the chiral catalyst may serve as a bifunctional reagent by interacting with both a carboxylic acid nucleophile and NBS electrophile.
Halogenation using quaternary ammonium polyhalides. XX. Bromination of phenols with polymer-bound benzyltrimethylammonium tribromide
Kakinami,Suenaga,Yamaguchi,Okamoto,Kajigaeshi
, p. 3373 - 3375 (2007/10/02)
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