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1-Propanone, 3-[(2-aminophenyl)amino]-1,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102318-17-2

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102318-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102318-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,1 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102318-17:
(8*1)+(7*0)+(6*2)+(5*3)+(4*1)+(3*8)+(2*1)+(1*7)=72
72 % 10 = 2
So 102318-17-2 is a valid CAS Registry Number.

102318-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(α-phenacylbenzyl)-o-phenylenediamine

1.2 Other means of identification

Product number -
Other names 3-(2-Amino-anilino)-1,3-diphenyl-propan-1-on

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:102318-17-2 SDS

102318-17-2Relevant academic research and scientific papers

H5CoW12O40@nanosilica: A green, bifunctional, heterogeneous nanocatalyst for one-pot three-component Mannich reaction in water

Rafiee, Ezzat,Kahrizi, Masoud

, p. 2833 - 2839 (2015)

Abstract 12-Tungestocobaltic acid, H5CoW12O40, was immobilized on nanosilica from rice husk ash to produce H5CoW12O40@nanosilica as a bifunctional nanocatalyst. The TEM result showed that the particles are mostly spherical in shape, and that they have an average size of approximately 10 nm. The catalytic activity of this catalyst was investigated in Mannich reaction of various aldehydes, ketones, and amines in water. This rapid procedure afforded structurally diverse β-amino ketones in high to excellent yields. Short reaction time, simple work-up procedure, elimination of toxic solvents, and low catalyst loading are the advantages of this procedure.

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