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5-Isoxazolepropanoic acid, b-(acetyloxy)-a-methylene-3-phenyl, ethyl ester is a complex organic compound with the chemical formula C16H15NO5. It is a derivative of isoxazolepropanoic acid, featuring an ethyl ester group, an acetyloxy group, and a methylene bridge connecting the isoxazole ring to a phenyl group. 5-Isoxazolepropanoic acid, b-(acetyloxy)-a-methylene-3-phenyl-, ethyl ester is known for its potential applications in pharmaceuticals and as a chemical intermediate in the synthesis of various drugs and agrochemicals. Its structure provides a unique set of properties that can be exploited in the design of new molecules with specific biological activities.

337356-13-5

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337356-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 337356-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,7,3,5 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 337356-13:
(8*3)+(7*3)+(6*7)+(5*3)+(4*5)+(3*6)+(2*1)+(1*3)=145
145 % 10 = 5
So 337356-13-5 is a valid CAS Registry Number.

337356-13-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[Acetoxy-(3-phenyl-isoxazol-5-yl)-methyl]-acrylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names -

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

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More Details:337356-13-5 SDS

337356-13-5Relevant academic research and scientific papers

Baylis-Hillman reaction assisted parallel synthesis of 3,5-disubstituted isoxazoles and their in vivo bioevaluation as antithrombotic agents

Batra,Roy,Patra,Bhaduri,Surin,Raghavan,Sharma,Kapoor,Dikshit

, p. 2059 - 2077 (2007/10/03)

The solution-phase parallel synthesis involving reactions of Baylis-Hillman products of 3-substituted-5-isoxazolecarbaldehydes with nucleophiles and their in vivo antithrombotic evaluations are described along with the results of in vitro platelet aggregation inhibition assay of a few compounds. Results of the detailed evaluation of one of the compounds as an inhibitor of platelet aggregation are also presented.

5-Isoxazolecarboxaldehyde: A novel substrate for fast Baylis-Hillman reaction

Patra,Batra,Kundu,Joshi,Roy,Bhaduri

, p. 276 - 280 (2007/10/03)

3-Aryl-5-isoxazolecarboxaldehyde undergoes fast Baylis-Hillman reaction with a variety of activated alkenes to yield the corresponding adducts in excellent yields. Some of the Baylis-Hillman adducts reported herein have been subsequently modified to obtai

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