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87351-03-9

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87351-03-9 Usage

Molecular structure

A symmetrical ketone with four phenyl groups attached to a pentane backbone

Usage

a. Precursor in the synthesis of various pharmaceuticals and organic materials
b. Synthetic intermediate in organic chemistry reactions
c. Fragrance ingredient in perfumes and personal care products
d. Production of dyes
e. Reagent in chemical laboratories

Physical state

White, crystalline solid at room temperature

Odor

Distinct aromatic odor

Check Digit Verification of cas no

The CAS Registry Mumber 87351-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,5 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87351-03:
(7*8)+(6*7)+(5*3)+(4*5)+(3*1)+(2*0)+(1*3)=139
139 % 10 = 9
So 87351-03-9 is a valid CAS Registry Number.

87351-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,5,5-tetraphenylpentan-3-one

1.2 Other means of identification

Product number -
Other names Dibenzhydrylaceton

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:87351-03-9 SDS

87351-03-9Relevant articles and documents

Palladium-Catalyzed Conjugate Addition Type Reaction of Aryl Iodides with α,β-Unsaturated Ketones

Cacchi, S.,Arcadi, A.

, p. 4236 - 4240 (2007/10/02)

Aryl iodides have been found to react with α,β-unsaturated ketones in the presence of catalytic amounts of palladium, an excess of formic acid, and triethylamine, giving rise to conjugate addition type products.The electron-withdrawing power of the group attached to the olefinic double bond, the substituent β to the carbonyl group, and the basic reaction medium appear to effect greatly the conjugate addition/vinylic substitution ratio.

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