170235-19-5 Usage
Description
Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate is a chemical compound with the molecular formula C8H7BrNO4. It is a derivative of pyridinecarboxylate and contains a bromine and a hydroxyl group in its structure. methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate is a valuable compound in organic chemistry research and is utilized in the development of various medicinal and agricultural products.
Uses
Used in Pharmaceutical Industry:
Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate is used as an intermediate in the synthesis of pharmaceuticals for its potential biological activities, including antimicrobial and antiviral properties. Its unique structure allows it to be a key component in the development of new drugs and therapies.
Used in Agrochemical Industry:
Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate is also used as an intermediate in the synthesis of agrochemicals. Its potential biological activities make it a useful compound in the development of pesticides, herbicides, and other agricultural products to improve crop yield and protect against diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 170235-19-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,2,3 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 170235-19:
(8*1)+(7*7)+(6*0)+(5*2)+(4*3)+(3*5)+(2*1)+(1*9)=105
105 % 10 = 5
So 170235-19-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BrNO3/c1-12-7(11)4-2-3-5(10)6(8)9-4/h2-3,10H,1H3
170235-19-5Relevant articles and documents
DI-MACROCYCLES
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Paragraph 00201, (2014/06/11)
The invention relates to chemical compounds and complexes that can be used in therapeutic and diagnostic applications.
Total synthesis of dimethyl sulfomycinamate
Ross Kelly,Lang, Fengrui
, p. 5319 - 5322 (2007/10/02)
The first total synthesis of dimethyl sulfomycinamate (1) is described. Highlights of the synthesis include a selective palladium-catalyzed coupling reaction on the bromotriflate 21, and a condensation reaction to form the oxazole ring.