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

116178-05-3

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116178-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116178-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,7 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116178-05:
(8*1)+(7*1)+(6*6)+(5*1)+(4*7)+(3*8)+(2*0)+(1*5)=113
113 % 10 = 3
So 116178-05-3 is a valid CAS Registry Number.

116178-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 3,6-diphenyl-as-triazine-5-carbonitrile

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:116178-05-3 SDS

116178-05-3Relevant academic research and scientific papers

One-step synthesis of 1,4-bis(het)arylisoquinolines by the reaction of 1,2,4-triazines with arynes

Kopchuk, Dmitry S.,Nikonov, Igor L.,Khasanov, Albert F.,Gundala, Sravya,Krinochkin, Alexey P.,Slepukhin, Pavel А.,Zyryanov, Grigory V.,Venkatapuram, Padmavathi,Chupakhin, Oleg N.,Charushin, Valery N.

, p. 978 - 984 (2019/11/16)

[Figure not available: see fulltext.] The reaction of 3,6-bis(het)aryl-1,2,4-triazines (hetaryl ≠ 2-pyridyl) with aryne intermediates generated in situ was studied. As a result, novel 1,4-bis(het)arylisoquinolines were synthesized with yields of up to 45%. The main rules of the reactions were studied, and the obtained experimental data were compared with those described in the literature.

Transformations of 1,2,4-triazines in reactions with nucleophiles: V. SNH and ipso-substitution in the synthesis and transformations of 5-cyano-1,2,4-triazines

Kozhevnikov,Kozhevnikov,Kovalev,Rusinov,Chupakhin,Aleksandrov

, p. 744 - 750 (2007/10/03)

The scope of functionalization of 1,2,4-triazines can be considerably extended via successive nucleophilic substitution of hydrogen (S NH) and ipso-substitution. A convenient procedure has been developed for direct cyanation of 1,2,4-triazine 4-oxides with acetone cyanohydrin in the presence of triethylamine. The cyano group in the resulting 5-cyano-1,2,4-triazines is readily replaced by reactions with various aliphatic alcohols and amines.

STUDIES ON as-TRIAZINE DERIVATIVES. VIII. SYNTHESIS OF 5-SUBSTITUTED 1,2,4-TRIAZINES

Konno, Shoetsu,Ohba, Setsuya,Agata, Mitsuko,Aizawa, Yuichi,Sagi, Mataichi,Yamanaka, Hiroshi

, p. 3259 - 3264 (2007/10/02)

Dehydroxy-chlorination of 6-methyl-3-phenyl (3a), and 3,6-diphenyl-5-oxo-2,5-dihydro-1,2,4-triazine (3b) afforded the corresponding 5-chloro-1,2,4-triazines (4a,b).The chloro-1,2,4-triazines (4a,b) treated with sodium alkoxides or amines to give the 5-alk

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