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76618-48-9

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76618-48-9 Usage

Chemical structure

A chalcone derivative with a propanone backbone, phenyl group, and phenylselanyl group attached.

Potential applications

Medicinal chemistry, specifically in the development of new drugs and pharmaceuticals.

Phenylselanyl group

Of interest due to its potential biological and pharmacological activities.

Usage

As a building block for the synthesis of novel organic molecules with therapeutic properties.

Research value

Valuable target for further research in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 76618-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,1 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76618-48:
(7*7)+(6*6)+(5*6)+(4*1)+(3*8)+(2*4)+(1*8)=159
159 % 10 = 9
So 76618-48-9 is a valid CAS Registry Number.

76618-48-9SDS

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 1,3-diphenyl-3-phenylselanylpropan-1-one

1.2 Other means of identification

Product number -
Other names 1,3-Diphenyl-3-phenylselanyl-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:76618-48-9 SDS

76618-48-9Downstream Products

76618-48-9Relevant articles and documents

-

Gilman,Cason

, p. 1074 (1951)

-

Ceric ammonium nitrate (CAN) as a green and highly efficient promoter for the 1,4-addition of thiols and benzeneselenol to α,β-unsaturated ketones

Chu, Cheng-Ming,Gao, Shijay,Sastry,Kuo, Chun-Wei,Lu, Chaowei,Liu, Ju-Tsung,Yao, Ching-Fa

, p. 1863 - 1871 (2007/10/03)

A mild and efficient process for the 1,4-addition of thiols and benzeneselenols to various α,β-unsaturated ketones using a catalytic amount of CAN with excellent product yields is described. This inexpensive, nontoxic, and readily available catalytic ceric(IV) ammonium nitrate system efficiently catalyzes conjugate addition reactions between thiol derivatives and various α,β-unsaturated ketones under solvent-free conditions. A plausible mechanism for the role of CAN, both as a promoter in free radical chain addition reactions as well as a catalyst for the conjugate addition process is proposed.

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