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14677-21-5

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14677-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14677-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,7 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14677-21:
(7*1)+(6*4)+(5*6)+(4*7)+(3*7)+(2*2)+(1*1)=115
115 % 10 = 5
So 14677-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H11NO/c1-3-7-12(8-4-1)14-11-16-17-15(14)13-9-5-2-6-10-13/h1-11H

14677-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-diphenyl-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 4,5-Diphenyl-isoxazol

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:14677-21-5 SDS

14677-21-5Relevant articles and documents

The chemistry of α,β-ditosyloxy ketones: A new and convenient route to 4,5-diarylisoxazoles from α,β-chalcone ditosylates

Kamal, Raj,Sharma, Deepak,Wadhwa, Deepak,Prakash, Om

experimental part, p. 93 - 96 (2012/02/03)

The reaction of α,β-chalcone ditosylates with hydroxyl-amine hydrochloride under suitable conditions leads to a 1,2-aryl shift, thereby providing a new route to 4,5-disubstituted isoxazoles. Georg Thieme Verlag Stuttgart. New York.

A convenient one-pot preparative method for 4,5-diarylisoxazoles involving amine exchange reactions

Dominguez, Esther,Ibeas, Estibaliz,De Marigorta, Eduardo Martinez,Palacios, Jon Kepa,SanMartin, Raul

, p. 5435 - 5439 (2007/10/03)

4,5-Diarylisoxazoles 1 are efficiently prepared by submitting enaminones 2, readily obtained from deoxybenzoins 3, to oximation conditions. This conversion implies an uncommon amine group exchange reaction. Preparation of 4-isoxazolines 5 and ring-opening transformations to β-keto nitriles 4 and 1,3-amino alcohol derivatives 7 are also described.

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