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4H-[1]Benzopyrano[3,4-d]isoxazol-4-one, 3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64517-78-8

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64517-78-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64517-78-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,1 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64517-78:
(7*6)+(6*4)+(5*5)+(4*1)+(3*7)+(2*7)+(1*8)=138
138 % 10 = 8
So 64517-78-8 is a valid CAS Registry Number.

64517-78-8SDS

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 3-phenylchromeno[3,4-d][1,2]oxazol-4-one

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:64517-78-8 SDS

64517-78-8Relevant articles and documents

A Convenient Synthesis of 3-Aryl-4H-benzopyranoisoxazol-4-ones

Litinas, Konstantinos E.,Nicolaides, Demetrios N.,Varella, Evangelia A.

, p. 769 - 774 (2007/10/02)

Regioselective 1,3-dipolar cycloaddition of nitrile oxides 5a-c to ethyl o-hydroxycinnamate (3) gave the corresponding ethyl trans-3-aryl-4,5-dihydro-5-(2-hydroxyphenyl)-4-isoxazolecarboxylates 6a-c.Their structure was confirmed by reductive cleavage to 1 and compounds 9a-c.Compounds 6a-c afforded upon heating in the presence of pyridine the 3-aryl-4H-benzopyranoisoxazol-4-ones 11a-c.Compound 10c was also isolated from 6c and transformed thermally into 11c.

Synthesis of Benzopyranoisoxazol-4-ones from 2-Substituted Chromone-3-carboxylic Esters. A Reinvestigation of the Reaction of 3-Acetyl-4-hydroxycoumarins with Hydroxylamine. Synthesis of 4-(2-Hydroxybenzoyl)isoxazol-5-ones

Chantegrel, Bernard,Nadi, Abdel Ilah,Gelin, Suzanne

, p. 4419 - 4424 (2007/10/02)

A convenient method for the synthesis of ethyl 2-substituted chromone-3-carboxylates by the condensation of o-acetoxyaroyl chlorides with β-keto esters is described.These chromones are converted into the corresponding 4H-benzopyranoisoxazol-4-on

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