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3-Isoxazolecarboxylic acid, 4,5-dihydro-, methyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50491-29-7

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50491-29-7 Usage

Chemical Group

Isoxazole carboxylic acid esters

Role

Methyl ester derivative of 3-isoxazolecarboxylic acid, 4,5-dihydro-

Applications

Used in pharmaceuticals, agrochemicals, organic synthesis, and medicinal chemistry

Physical Appearance

White to off-white solid

Variability

Properties and applications may vary based on concentration and formulation.

Check Digit Verification of cas no

The CAS Registry Mumber 50491-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,9 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50491-29:
(7*5)+(6*0)+(5*4)+(4*9)+(3*1)+(2*2)+(1*9)=107
107 % 10 = 7
So 50491-29-7 is a valid CAS Registry Number.

50491-29-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 3-Isoxazolecarboxylic acid,4,5-dihydro-,methyl ester

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:50491-29-7 SDS

50491-29-7Downstream Products

50491-29-7Relevant academic research and scientific papers

REACTIONS OF DIMETHYL 2-METHOXYISOXAZOLIDINE-3,3-DICARBOXYLATE CATALYZED BY LEWIS ACIDS

Rudchenko, V. F.,Voznesenskii, V. N.,Kostyanovskii, R. G.

, p. 96 - 102 (2007/10/02)

Evidence is presented for a synchronous mechanism of the acid-catalyzed 1,2-rearrangement of 2-methoxyisoxazolidine-2,3-dicarboxylic acid ester with migration of the ester group to the N-atom.It was shown that the reaction is suppressed in the presence of an external nucleophile or a reducing agent.The regularities found were used to explain the transformations of bicyclic systems with an -ONO-fragment.

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