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13073-28-4

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13073-28-4 Usage

General Description

3-Bromo-2-hydroxybenzonitrile is a chemical compound with the molecular formula C7H4BrNO. It is a pale yellow solid that is mainly used in the synthesis of pharmaceutical and agrochemical products. It is also used as a building block in the production of various organic compounds. The compound is known for its strong nucleophilic properties, making it a useful reagent in organic synthesis. It is also used as a precursor in the production of dyes and pigments. Additionally, it is considered to be relatively stable under normal conditions, making it a versatile and valuable chemical in various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 13073-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,7 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13073-28:
(7*1)+(6*3)+(5*0)+(4*7)+(3*3)+(2*2)+(1*8)=74
74 % 10 = 4
So 13073-28-4 is a valid CAS Registry Number.

13073-28-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H66401)  3-Bromo-2-hydroxybenzonitrile, 97%   

  • 13073-28-4

  • 1g

  • 658.0CNY

  • Detail
  • Alfa Aesar

  • (H66401)  3-Bromo-2-hydroxybenzonitrile, 97%   

  • 13073-28-4

  • 5g

  • 3024.0CNY

  • Detail

13073-28-4Relevant articles and documents

CRYSTALLINE FORMS OF SOMATOSTATIN MODULATORS

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Paragraph 00229, (2021/02/12)

Described herein are pharmaceutically acceptable salts of a somatostatin modulator, crystalline forms of the pharmaceutically acceptable salts of the somatostatin modulator, methods of making such salts and crystalline forms, pharmaceutical compositions and medicaments comprising such salts and crystalline forms, and methods of using such salts and crystalline forms in the treatment of conditions, diseases, or disorders that would benefit from modulation of somatostatin activity.

Chromatography-free entry to substituted salicylonitriles: Mitsunobu-triggered domino reactions of salicylaldoximes

Whiting, Ellis,Lanning, Maryanna E.,Scheenstra, Jacob A.,Fletcher, Steven

, p. 1229 - 1234 (2015/01/30)

A mild and efficient one-pot procedure is described to transform salicylaldoximes into salicylonitriles using Mitsunobu chemistry. The reactions proceed through the corresponding 1,2-benzisoxazoles that undergo the Kemp elimination in situ to generate the

NOVEL COMPOUNDS AS ANTAGONISTS OR INVERSE AGONISTS AT OPIOID RECEPTORS

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, (2011/06/19)

Novel compounds which are antagonists or inverse agonists at one or more of the opioid receptors, pharmaceutical compositions containing them, to processes for their preparation.

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