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77989-15-2

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77989-15-2 Usage

General Description

2-(2-bromophenyl)-4,6-diphenyl-1,3,5-triazine is a chemical compound with the molecular formula C21H14BrN3. It belongs to the class of triazine compounds and contains a triazine ring with two phenyl groups and a bromophenyl group attached to it. 2-(2-bromophenyl)-4,6-diphenyl-1,3,5-triazine has potential applications in organic synthesis and material science due to its unique structure and properties. It may also have potential pharmaceutical and biological activities, although further research is needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 77989-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,8 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77989-15:
(7*7)+(6*7)+(5*9)+(4*8)+(3*9)+(2*1)+(1*5)=202
202 % 10 = 2
So 77989-15-2 is a valid CAS Registry Number.

77989-15-2SDS

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 2-(o-bromophenyl)-4,6-diphenyl-1,3,5-triazine

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:77989-15-2 SDS

77989-15-2Downstream Products

77989-15-2Relevant articles and documents

Nitrogen-containing compound, electronic element, and electronic device

-

Paragraph 0197-0200; 0218, (2020/07/24)

The invention belongs to the technical field of organic materials, and provides a nitrogen-containing compound, an electronic element and an electronic device. The structure of the nitrogen-containingcompound is shown as a formula 1, wherein X1, X2 and X3 are respectively and independently selected from C or N, and at least one of X1, X2 and X3 is N; wherein R1, R2 and R3 are respectively and independently selected from hydrogen or a group shown in a chemical formula 1-1, and only one of R1, R2 and R3 is a group shown in a chemical formula 1-1. The nitrogen-containing compound can improve theperformance of an electronic component.

Sulfur Nitride in Organic Chemistry. 9. The Reaction of Tetrasulfur Tetranitride with Benzyl Ketones. Preparation of 3,4-Disubstituted-1,2,5-thiadiazoles

Mataka, Shuntaro,Hosoki, Akira,Takahashi, Kazufumi,Tashiro, Masashi

, p. 1681 - 1685 (2007/10/02)

The reaction of tetrasulfur tetranitride (1) with various aryl and benzyl ketones (2a-o), oxindole (11), benzyl α-pyridyl ketone (12) and α-phenacylpyridine (13) afforded the corresponding 1,2,5-thiadiazoles (3a-n, 11 and 14).The scope and limitations of the above reaction were investigated and the evidences suggesting the radical anion mechanism are presented.

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