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105174-97-8

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105174-97-8 Usage

General Description

Ethyl 3-bromoisoxazole-5-carboxylate is a synthetic, organic chemical compound whose molecular structure features an isoxazole ring (a five-membered heterocyclic ring compound containing three carbon atoms, one oxygen atom, and one nitrogen atom) as well as a carboxylate group and a bromine atom. It has a molecular weight of 246.02 g/mol. Due to its intriguing molecular structure, this chemical is often used in research and development, especially in the field of medicinal chemistry where it may act as a building block in the creation of various pharmaceutical drugs. As with other chemicals, it should be handled with care, following appropriate safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 105174-97-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,1,7 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105174-97:
(8*1)+(7*0)+(6*5)+(5*1)+(4*7)+(3*4)+(2*9)+(1*7)=108
108 % 10 = 8
So 105174-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BrNO3/c1-2-10-6(9)4-3-5(7)8-11-4/h3H,2H2,1H3

105174-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3-bromoisoxazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 3-bromo-1,2-oxazole-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:105174-97-8 SDS

105174-97-8Relevant articles and documents

Process for the preparation of 3,5-disubstituted isoxazoles

-

, (2008/06/13)

A novel process for the preparation of 3-bromo- and 3-chloro-5-substituted isoxazoles is provided. Dibromo- or dichloro-formaldoxime is reacted with an excess of an 1-alkyne derivative of the formula where R is hydrogen, phenyl or 1-6 C alkyl optionally substituted by halogen, OH, OR', CHO, COR', COOR', CONH2, CONR'R" or NHCOR' where, in turn, R' and R", which may be the same or different, are a 1-6 C alkyl or haloalkyl, in the presence of (i) at least an equimolecular amount, with respect to the dibromo- or dichloro-formaldoxime, of an alkaline base selected from the class consisting of sodium and potassium carbonate and bicarbonate and (ii) an inert solvent in which the 1-alkyne is soluble at room temperature.

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