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672948-03-7

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672948-03-7 Usage

Uses

2-Oxazolecarboxylic acid is used as a reagent to prepare 3-(5-Chloro-2-furoyl)-3,7-diazabicyclo[3.3.0]octane, a highly selective α4β2 nicotinic Acetylcholine (A172060) receptor agonist used in the treatment of cognitive disorders such as Alzheimer’s disease.

Check Digit Verification of cas no

The CAS Registry Mumber 672948-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,2,9,4 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 672948-03:
(8*6)+(7*7)+(6*2)+(5*9)+(4*4)+(3*8)+(2*0)+(1*3)=197
197 % 10 = 7
So 672948-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H3NO3/c6-4(7)3-5-1-2-8-3/h1-2H,(H,6,7)

672948-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Oxazole-2-Carboxylic Acid

1.2 Other means of identification

Product number -
Other names 1,3-oxazole-2-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:672948-03-7 SDS

672948-03-7Relevant articles and documents

CARBOXYLATION CATALYSTS

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Paragraph 0086; 0087, (2013/04/13)

The use of a complex of the form Z—M—OR in the carboxylation of a substrate is described. The group Z is a two-electron donor ligand, M is a metal and OR is selected from the group consisting of OH, alkoxy and aryloxy. The substrate may be carboxylated at a C—H or N—H bond. The metal M may be copper, silver or gold. The two-electron donor ligand may be a phosphine, a carbene or a phosphite ligand. Also described are methods of manufacture of the complexes and methods for preparing isotopically labelled caboxylic acids and carboxylic acid derivatives.

Carboxylation of N-H/C-H bonds using n-heterocyclic carbene copper(I) complexes

Boogaerts, Ine I. F.,Fortman, George C.,Furst, Marc R. L.,Cazin, Catherine S. J.,Nolan, Steven P.

supporting information; scheme or table, p. 8674 - 8677 (2011/01/06)

Greenhouse gas makes good: A simple copper-mediated protocol has been developed where N-H or C-H bonds can be directly functionalized using an easily prepared catalyst. The novel [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene] copper(I) hydroxide, [Cu(IPr)(OH)], permits the facile activation and carboxylation of N-H and C-H bonds with pKavalues of less than 27.7 (see scheme).

Phenyl-isoxazoles as factor XA Inhibitors

-

, (2008/06/13)

The present application describes oxygen and sulfur containing heteroaromatics and derivatives thereof of formula or pharmaceutically acceptable salt or prodrug forms thereof, wherein J is O or S and D may be C(=NH)NH2, which are useful as inhibitors of factor Xa.

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