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1,4,3-Oxaselenazine, 4,4,5,6-tetrahydro-2,6-diphenyl-4-[(phenylsulfonyl)imino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87786-72-9

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87786-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87786-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,8 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87786-72:
(7*8)+(6*7)+(5*7)+(4*8)+(3*6)+(2*7)+(1*2)=199
199 % 10 = 9
So 87786-72-9 is a valid CAS Registry Number.

87786-72-9SDS

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 2,6-diphenyl-4-phenylsulfonylimino-5,6-dihydro-4,1,3-selenaoxazine

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:87786-72-9 SDS

87786-72-9Relevant academic research and scientific papers

N-AROYLDICHLOROSELENIMIDES

Derkach, N. Ya.,Krasnyanskaya, T. V.,Levchenko, E. S.,Zabolotnaya, T. G.

, p. 2167 - 2171 (2007/10/02)

N-Aroyldichloroselenimides were obtained in the reaction of selenium with N,N-dichloroaroylamines.The products react with olefins by a mechanism of the -cycloaddition type with the formation of substituted 4,4-dichloro-5,6-dihydro-4,1,3-selenaoxazines.

REACTION OF N-SUBSTITUTED N'-ACYLSELENIUM DIIMIDES WITH OLEFINS

Derkach, N. Ya.,Barashenkov, G. G.,Levchenko, E. S.

, p. 1435 - 1438 (2007/10/02)

N-Substituted N'-acylselenium diimides, which contain a Se=N-C=O group, react with olefins by a 1,4-cycloaddition mechanism with the formation of the corresponding substituted 4-imino-5,6-dihydro-4,1,3-selenaoxazines.

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