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54322-81-5

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54322-81-5 Usage

Class of compound

Ketone

Structural features

Contains a cyclopentanone ring with a 3-phenylpropylidene group attached

Usage

Commonly used in organic synthesis and research as a reagent or intermediate in the production of pharmaceuticals and other organic compounds

Importance

Unique structure makes it useful for the development of new materials and chemical processes in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 54322-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,2 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54322-81:
(7*5)+(6*4)+(5*3)+(4*2)+(3*2)+(2*8)+(1*1)=105
105 % 10 = 5
So 54322-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H16O/c15-14-11-5-10-13(14)9-4-8-12-6-2-1-3-7-12/h1-3,6-7,9H,4-5,8,10-11H2

54322-81-5SDS

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 2-[3-Phenyl-prop-(E)-ylidene]-cyclopentanone

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:54322-81-5 SDS

54322-81-5Downstream Products

54322-81-5Relevant articles and documents

Tandem hydroformylation/aldol condensation reactions: Synthesis of unsaturated ketones from olefins

Kollár, László,Pongrácz, Péter

, p. 184 - 188 (2018/05/07)

Platinum-catalysed tandem hydroformylation/aldol condensation reaction of vinyl aromatics and ketones toward the corresponding α,β-unsaturated ketones were performed under syngas atmosphere in the presence of acid co-catalysts. The in situ generated catal

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