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38076-80-1

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38076-80-1 Usage

Synthesis Reference(s)

Synthetic Communications, 19, p. 553, 1989 DOI: 10.1080/00397918908050699

Check Digit Verification of cas no

The CAS Registry Mumber 38076-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,7 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38076-80:
(7*3)+(6*8)+(5*0)+(4*7)+(3*6)+(2*8)+(1*0)=131
131 % 10 = 1
So 38076-80-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClNO3/c7-3-1-4(6(10)11)5(9)8-2-3/h1-2H,(H,8,9)(H,10,11)/p-1

38076-80-1 Well-known Company Product Price

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  • Alfa Aesar

  • (B20706)  5-Chloro-2-hydroxynicotinic acid, 97%   

  • 38076-80-1

  • 1g

  • 304.0CNY

  • Detail
  • Alfa Aesar

  • (B20706)  5-Chloro-2-hydroxynicotinic acid, 97%   

  • 38076-80-1

  • 5g

  • 1127.0CNY

  • Detail
  • Alfa Aesar

  • (B20706)  5-Chloro-2-hydroxynicotinic acid, 97%   

  • 38076-80-1

  • 25g

  • 4550.0CNY

  • Detail

38076-80-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Chloro-2-hydroxynicotinic Acid

1.2 Other means of identification

Product number -
Other names 5-chloro-2-oxo-1H-pyridine-3-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:38076-80-1 SDS

38076-80-1Relevant articles and documents

SUBSTITUTED NAPHTHYRIDINE DERIVATIVES AS INHIBITORS OF MACROPHAGE MIGRATION INHIBITORY FACTOR AND THEIR USE IN THE TREATMENT OF HUMAN DISEASES

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Page/Page column 121; 186-187, (2010/02/11)

Inhibitors of MIF having a naphthyridine backbone are provided which have utility in the treatment of a variety of disorders, including the treatment of pathological conditions associated with MIF activity. The inhibitors of MIF have the following structures: (Ia), (Ib), (Ic), (Id) including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof, wherein n, R, R1, R2, X, Y and Z are as defined herein. Compositions containing an inhibitor of MIF in combination with a pharmaceutically acceptable carrier are also provided, as well as methods for use of the same.

Process for the preparation of 5-chloro and 5-bromo-2-hydroxynicotinic acids

-

, (2008/06/13)

A process for the preparation of 5-halo-2-hydroxynicotinic acids having the formula: STR1 wherein X is chlorine or bromine, Y and Z are selected from hydrogen, loweralkyl or loweralkyl, is described wherein a corresponding 2-hydroxynicotinic acid is halogenated with alkali-metal hypohalite in a strongly alkaline solution pH 12 and above. Certain aspects of the isolation of the product are directed to avoiding replacement of the carboxy group with halogen.

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