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78650-07-4

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78650-07-4 Usage

Properties

Chemical compound
Contains triazino and benzimidazol rings
Dihydro and amine groups attached
Presence of chlorophenyl group

Specific content

4-(2-chlorophenyl) group
1,4-dihydro[1,3,5]triazino[1,2-a][1,3]benzimidazol-2-amine structure
Potential applications in medicinal chemistry
Unique molecular features
Building block for synthesis of biologically-active compounds
Requires detailed study and analysis for understanding potential uses and effects

Check Digit Verification of cas no

The CAS Registry Mumber 78650-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,5 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78650-07:
(7*7)+(6*8)+(5*6)+(4*5)+(3*0)+(2*0)+(1*7)=154
154 % 10 = 4
So 78650-07-4 is a valid CAS Registry Number.

78650-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-CHLOROPHENYL)-1,4-DIHYDRO[1,3,5]TRIAZINO[1,2-A][1,3]BENZIMIDAZOL-2-AMINE

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:78650-07-4 SDS

78650-07-4Downstream Products

78650-07-4Relevant articles and documents

Synthesis of ethyl 6-aryl-4-oxo-4,6-dihydro-1(12)(13)H-pyrimido-[2′, 1′:4,5][1,3,5]triazino[1,2-a]benzimidazole-3-carboxylates

Dolzhenko, Anton V.,Chui, Wai-Keung,Dolzhenko, Anna V.

, p. 1513 - 1521 (2007/10/03)

The synthesis of ethyl 6-aryl-4-oxo-4,6-dihydro-1(12)(13)H- pyrimido[2′,1′:4,5][1,3,5]triazino[1,2-a]-benzimidazole-3- carboxylates (4a-p) was described via pyrimidine ring annulation to 4-aryl-3,4-dihydro[1,3,5]triazino[1,2-a]benzimidazole-2-amines (2a-p

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