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15055-81-9

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15055-81-9 Usage

Uses

5-Isoxazolecarboxylic Acid Methyl Ester is used as a reagent in the synthesis of pyridine derivatives as integrase inhibitors and antiviral agents. 5-Isoxazolecarboxylic Acid Methyl Ester is also a useful synthetic intermediate in the preparation of pyrazolopyrimidine derivatives useful in the prevention and treatment of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 15055-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,5 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15055-81:
(7*1)+(6*5)+(5*0)+(4*5)+(3*5)+(2*8)+(1*1)=89
89 % 10 = 9
So 15055-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H5NO3/c1-8-5(7)4-2-3-6-9-4/h2-3H,1H3

15055-81-9 Well-known Company Product Price

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  • Alfa Aesar

  • (B25169)  Methyl isoxazole-5-carboxylate, 97%   

  • 15055-81-9

  • 1g

  • 709.0CNY

  • Detail
  • Alfa Aesar

  • (B25169)  Methyl isoxazole-5-carboxylate, 97%   

  • 15055-81-9

  • 5g

  • 2602.0CNY

  • Detail
  • Alfa Aesar

  • (B25169)  Methyl isoxazole-5-carboxylate, 97%   

  • 15055-81-9

  • 25g

  • 10585.0CNY

  • Detail

15055-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl Isoxazole-5-Carboxylate

1.2 Other means of identification

Product number -
Other names METHYL ISOXAZOLE-5-CARBOXYLATE

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:15055-81-9 SDS

15055-81-9Relevant articles and documents

Carboxylation of C-H bonds using N -heterocyclic carbene gold(I) complexes

Boogaerts, Ine I. F.,Nolan, Steven P.

supporting information; experimental part, p. 8858 - 8859 (2010/08/21)

A highly efficient [(NHC)AuI]-based (NHC = N-heterocyclic carbene) catalytic system for the carboxylation of aromatic and heteroaromatic C-H bonds was developed. The significant base strength of the Au-OH species is at the origin of the activation process and permits the facile functionalization of C-H bonds without the use of other organometallic reagents.

INTEGRASE INHIBITORS 3

-

Page/Page column 61, (2008/06/13)

The present invention provides a method of treatment or prophylaxis of a viral infection in a subject comprising administering to said subject an effective amount of a compound of formula (I) or a pharmaceutically acceptable derivative, salt or prodrug thereof. Compounds of formula (I) are also provided.

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