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
77614-53-0Relevant articles and documents
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
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.
