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Cyclobutane, also known as ethynyl-cyclobutane, is a cyclic hydrocarbon compound with the molecular formula C6H8. It consists of a four-membered ring structure with two carbon-carbon triple bonds (acetylene groups) attached to two of the carbon atoms in the ring. This unique structure makes cyclobutane an interesting molecule for study in organic chemistry, as it exhibits properties different from those of other cyclic hydrocarbons due to its strained ring and the presence of acetylene groups. Cyclobutane has potential applications in various fields, including pharmaceuticals, materials science, and chemical synthesis, where its unique properties can be exploited for specific reactions or processes.

2597-49-1

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2597-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2597-49-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2597-49:
(6*2)+(5*5)+(4*9)+(3*7)+(2*4)+(1*9)=111
111 % 10 = 1
So 2597-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H10/c1-2-6-4-3-5-6/h2,6H,1,3-5H2

2597-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethenylcyclobutane

1.2 Other means of identification

Product number -
Other names Cyclobutane,vinyl

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:2597-49-1 SDS

2597-49-1Relevant academic research and scientific papers

Alkynes and Cumulenes, XVII, Photoaddition of Vinylacetylene to other Unsaturated Hydrocarbons

Siegel, Herbert,Eisenhuth, Ludwig,Hopf, Henning

, p. 597 - 612 (2007/10/02)

On irradiation in the presence of triplet sensitizers, vinylacetylene (1) may be added with its double bond to olefins , dienes , allenes , and diynes .The resulting multifunctionalized cyclobutane derivatives are characterized by spectroscopic and chemical methods.Since the ethinyl group of these codimers may be hydrated to the acetyl function, 1 represents a photochemical equivalent of methyl vinyl ketone which itself does not undergo the described photoadditions.When benzene (56) is employed as addition partner the primary product of the codimerisation, 54, isomerizes to vinylcyclooctatetraene (55).

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