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1,2,4-Triazine, 3-azido-5,6-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88281-91-8

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88281-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88281-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,8 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88281-91:
(7*8)+(6*8)+(5*2)+(4*8)+(3*1)+(2*9)+(1*1)=168
168 % 10 = 8
So 88281-91-8 is a valid CAS Registry Number.

88281-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-azido-5,6-diphenyl-1,2,4-triazine

1.2 Other means of identification

Product number -
Other names 1,2,4-Triazine,3-azido-5,6-diphenyl

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:88281-91-8 SDS

88281-91-8Relevant academic research and scientific papers

Synthesis and reactions of 1,2,4-triazine azides with triphenylphosphine, trialkyl phosphites and dialkyl phosphonates

El-Khoshnieh, Yehia O.

, p. 163 - 172 (2007/10/03)

3-Azido-5,6-diphenyl-1,2,4-triazine (1) and 3-azidophenanthro[9,10-e]-1,2,4-triazine (2) are synthesized in high yield (-75%), 1 and 2 react with triphenylphosphine to afford phosphazenes 5 and 6 with a covalent structure. Reactions of 1 and 2 with trialkyl phosphites 3b,c produce phosphazenes 7a,b and 8a,b which have the phosphonium dipolar ion structure, 1 reacts with diethyl phosphonate (4a) to give the phosphoramidate 10a, dissociating to the corresponding amine 11 on reaction with dimethyl phosphonate. Possible reaction mechanisms are proposed for the formation of the new adducts.

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