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METHYL 3-BROMO-5-METHYLISOXAZOLE-4-CARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

188686-98-8

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188686-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188686-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,6,8 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 188686-98:
(8*1)+(7*8)+(6*8)+(5*6)+(4*8)+(3*6)+(2*9)+(1*8)=218
218 % 10 = 8
So 188686-98-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BrNO3/c1-3-4(6(9)10-2)5(7)8-11-3/h1-2H3

188686-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-bromo-5-methyl-1,2-oxazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names METHYL 3-BROMO-5-METHYLISOXAZOLE-4-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:188686-98-8 SDS

188686-98-8Relevant academic research and scientific papers

Efficient regioselective synthesis of 4- and 5-substituted isoxazoles under thermal and microwave conditions

Lasri, Jamal,Mukhopadhyay, Suman,Charmier, M. Adilia Januario

experimental part, p. 1385 - 1389 (2009/04/10)

(Chemical Equation Presented) The [2+3] cycloaddition reaction between nitrile oxides 2 and the captodative olefins 1 or the methyl crotonate derivatives 4 is regioselective and leads to the formation of the 5-substituted amino-isoxazole 3 or the 4-substi

An expedient synthesis of (±)-2-amino-3-(3-hydroxy-5-methylisoxazol-4-yl)propionic acid hydrobromide via a 3-bromoisoxazole intermediate

Hanson, Robert N.,Mohamed, Fand A.

, p. 345 - 348 (2007/10/03)

The excitatory, amino acid ± 2-amino-3-(3-hydroxy-5-methylisoxazol-4-yl)propionic acid hydrobromide was prepared in gram quantities in a 3.3% overall yield from methylbut 2-ynoate. The key step was the facile preparation of methyl 3-bromo-5-methylisoxazole-4-carboxylate.

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