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4-Propyl-1,3-cyclohexanedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18456-81-0

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18456-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18456-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,5 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18456-81:
(7*1)+(6*8)+(5*4)+(4*5)+(3*6)+(2*8)+(1*1)=130
130 % 10 = 0
So 18456-81-0 is a valid CAS Registry Number.

18456-81-0SDS

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 4-propylcyclohexane-1,3-dione

1.2 Other means of identification

Product number -
Other names 1,3-Cyclohexanedione,4-propyl

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:18456-81-0 SDS

18456-81-0Relevant academic research and scientific papers

Pyrazolopyridine cycloalkanones and process for their preparation

-

, (2008/06/13)

Novel tetrahydropyrazolo-[3,4-b]quinolinones, cyclopenta[b]pyrazolo-[4,3-e]pyridinones and cyclohepta[b]-pyrazolo[4,3-e]pyridinones, useful as anxiolytics having reduced side effects, are disclosed, including methods of preparation, pharmaceutical compositions containing them and intermediates used in their preparation.

Synthesis of β-chloro, β-bromo, and β-iodo α,β-unsaturated ketones

Piers, Edward,Grierson, John R.,Lau, Cheuk Kun,Nagakura, Isao

, p. 210 - 223 (2007/10/02)

A new, efficient method for the preparation of β-chloro, β-bromo, and β-iodo α,β-unsaturated ketones is described.The method involves the reaction of β-diketones or α-hydroxymethylenecycloalkanones with triphenylphosphine dihalides in the presence of trie

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