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2,3-dipropyl-2-cyclopropen-1-one is a chemical compound with the molecular formula C8H12O. It is a derivative of cyclopropenone, featuring two propyl groups attached to the 2 and 3 positions of the cyclopropane ring. 2,3-dipropyl-2-cyclopropen-1-one is known for its unique structure and reactivity, which can be attributed to the strained three-membered ring and the presence of a carbonyl group. It is often used in organic synthesis as a building block for more complex molecules, particularly in the preparation of various heterocyclic compounds. Due to its reactive nature, it is important to handle 2,3-dipropyl-2-cyclopropen-1-one with care, as it can undergo various chemical transformations, such as cycloadditions and rearrangements.

698-93-1

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698-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 698-93-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 698-93:
(5*6)+(4*9)+(3*8)+(2*9)+(1*3)=111
111 % 10 = 1
So 698-93-1 is a valid CAS Registry Number.

698-93-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dipropylcycloprop-2-en-1-one

1.2 Other means of identification

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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

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More Details:698-93-1 SDS

698-93-1Relevant academic research and scientific papers

An improved synthesis of dialkylcyclopropenones

Netland, Kjetil Andreas,Gundersen, Lise-Lotte,Rise, Frode

, p. 1767 - 1777 (2007/10/03)

Dialkylcyclopropenones are formed in high yields when alkynes are treated with chloroform-butyllithium in THF at - 78 °C followed by acidic hydrolysis of the dichlorocyclopropene intermediates at low temperatures.

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