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15069-92-8

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15069-92-8 Usage

Chemical Properties

Crystalline Solid

Uses

Different sources of media describe the Uses of 15069-92-8 differently. You can refer to the following data:
1. Useful synthetic intermediate. Also intermediate for pharmaceutical application.
2. 5-Hydroxypyridine-2-carboxylic acid is a useful synthetic intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 15069-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,6 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15069-92:
(7*1)+(6*5)+(5*0)+(4*6)+(3*9)+(2*9)+(1*2)=108
108 % 10 = 8
So 15069-92-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H5NO3/c8-4-1-2-5(6(9)10)7-3-4/h1-3,8H,(H,9,10)/p-1

15069-92-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H64265)  5-Hydroxypyridine-2-carboxylic acid, 98+%   

  • 15069-92-8

  • 1g

  • 196.0CNY

  • Detail
  • Alfa Aesar

  • (H64265)  5-Hydroxypyridine-2-carboxylic acid, 98+%   

  • 15069-92-8

  • 5g

  • 706.0CNY

  • Detail
  • Alfa Aesar

  • (H64265)  5-Hydroxypyridine-2-carboxylic acid, 98+%   

  • 15069-92-8

  • 25g

  • 2940.0CNY

  • Detail

15069-92-8Relevant articles and documents

A METHOD OF PRODUCING 5-HYDROXYPYRIDINE-2-CARBOXYLIC ACID FROM ALGINATE

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Page/Page column 22-23, (2012/11/06)

The present application provides methods for converting alginate into 5-hydroxypyridine- 2-carboxylic acid (5-HPA) using an alginate lyase and a recombinant oligoalginate lyase. The alginate lyase breaks down alginate into oligoalginate. The oligoalginate lyase breaks down the oligoalginate into monomers such as 4-deoxy-L-erythro-hexoseulose uronate (DEHU), which serves as a precursor for conversion into 5-HPA. The addition of ammonia or an ammonium ion further drives the conversion of DEHU into 5-HPA.

The preparation of Some 4- and 5-Substituted Pyridine-2-carboxylic Acids as Fusaric Acid Analogues.

Oehlke, J.,Schroetter, E.,Dove, S.,Schick, H.,Niedrich, H.

, p. 591 - 596 (2007/10/02)

In view of future studies on the structure-activity relationships involved in the inhibition of dopamine β-hydroxylase, the authors synthetized 5-substituted picolinic acids and 4-substituted fusaric acids selected by means of a random sampling procedure suited for small series.On this occasion, they succeeded in improving markedly the well-known synthesis of 5-nitropicolinic acid via a Rosenmund-v.Braun reaction with 2-bromo-5-nitropyridine. 5-Hydroxypicolinic acid which is easily accessible in the same way could be converted into 5-alkyloxypicolinic acids by reaction with alkyl halides in DMSO in the presence of silver oxide. 4-Substituted fusaric acids became accessible via 5-n-butyl-2-methyl-4-nitropyridine-N-oxide.

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