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

77614-53-0

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77614-53-0 Usage

Type of compound

Cyclic hydrocarbon

Structure

Contains double bonds and a four-membered ring

Physical state at room temperature

Colorless liquid

Flammability

Highly flammable

Usage

Organic synthesis

Reactivity

Reactive due to the presence of double bonds

Reactions

Can undergo addition reactions with other molecules

Applications

Building block for the synthesis of various organic compounds

Potential uses

Development of new materials and pharmaceuticals due to unique structure and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 77614-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,1 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77614-53:
(7*7)+(6*7)+(5*6)+(4*1)+(3*4)+(2*5)+(1*3)=150
150 % 10 = 0
So 77614-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12/c1-3-7-5-8(4-2)6-7/h3-4,7-8H,1-2,5-6H2

77614-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-1,3-Diethenylcyclobutane

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:77614-53-0 SDS

77614-53-0Relevant academic research and scientific papers

Pyrolysis and Photolysis of 6,7-Diazatricyclo2,4>dec-6-ene

Yin, Tyze-Kuan,Borden, Weston Thatcher

, p. 2285 - 2289 (2007/10/02)

Pyrolysis at 200 deg C and direct and sensitized photolysis of the title compound (3a) produced only cis-1,3-divinylcyclobutane (6a) and tricyclo2,5>octane (7a).The latter hydrocarbon was preapared by an independent synthesis, which inv

Ueber die Thermolyse von cis- und trans-1,3-Divinylcyclobutan

Schwarz, Wolfgang,Trautmann, Walter,Musso, Hans

, p. 990 - 993 (2007/10/02)

At 300 deg C cis-1,3-divinylcyclobutane (4) gives butadiene (5) and 4-vinyl-1-cyclohexene (6) as well as trans-1,3-divinylcyclobutane (2) in small quantity. 2 has been synthesized in an independent way and yields the same products as 4.The diradical 3 is

Zur Photochemie des cis-1,3-Divinylcyclobutans

Trautmann, Walter,Musso, Hans

, p. 982 - 989 (2007/10/02)

The title compound 7 is obtained by ozonolysis of bicyclohex-2-ene (5) and Wittig reaction of the dialdehyde 6.There was no intramolecular photo-cycloaddition observed by irradiation of 7 but rearrangement to cis- and trans-allylvinylcyclopropanes 10 and 11.With the esters 12 - 14 the light energy is wasted in cis-trans-isomerisations.In comparison, the cis-1,3-cyclopentane derivatives 16 and 17 give some cycloaddition.

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