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5227-55-4

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5227-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5227-55-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5227-55:
(6*5)+(5*2)+(4*2)+(3*7)+(2*5)+(1*5)=84
84 % 10 = 4
So 5227-55-4 is a valid CAS Registry Number.

5227-55-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diphenyl-Quinoxaline, 1-oxide

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:5227-55-4 SDS

5227-55-4Relevant articles and documents

Hypervalent iodine oxidation of benzil-α-arylimino oximes: an efficient synthesis of 2,3-diphenylquinoxaline-1-oxides

Aggarwal, Ranjana,Sumran, Garima,Saini, Anil,Singh, Shiv P.

, p. 4969 - 4971 (2007/10/03)

A mild and efficient synthetic protocol for the oxidation of benzil-α-arylimino oximes 3 utilizing iodobenzene diacetate (IBD) as an oxidizing agent has been developed. Oximes 3, obtained by the condensation of (E)-benzil monoxime 2 with various appropria

Synthesis of 2,3-diphenylquinoxaline 1-oxides by oxidative cyclization of benzil α-arylimino oximes

Maroulis,Domzaridou,Hadjiantoniou-Maroulis

, p. 1769 - 1772 (2007/10/03)

The title compounds-3a-h were synthesized by condensation of (E)-benzil monoxime 2 with the appropriate substituted aniline, 1 followed by oxidative cyclization to the corresponding 2,3-diphenylquinoxaline 1-oxides 4a-h using lead tetraacetate.

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