765-86-6 Usage
General Description
The chemical compound (5α,6α)-5,6-Dimethyl-1,3-cyclohexadiene is a cyclic hydrocarbon with a molecular formula of C8H12. It is a colorless liquid with a molecular weight of 108.18 g/mol. (5α,6α)-5,6-Dimethyl-1,3-cyclohexadiene contains a six-membered cyclohexadiene ring with two methyl groups attached to the carbon atoms in the 5th and 6th positions. (5α,6α)-5,6-Dimethyl-1,3-cyclohexadiene is used as a building block in organic synthesis and can undergo various reactions to form different compounds. Due to its cyclic structure and double bonds, it is a versatile compound with potential applications in the pharmaceutical, agrochemical, and material industries. It is important to handle (5α,6α)-5,6-Dimethyl-1,3-cyclohexadiene with care, as it is flammable and may pose health risks if inhaled or ingested.
Check Digit Verification of cas no
The CAS Registry Mumber 765-86-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 765-86:
(5*7)+(4*6)+(3*5)+(2*8)+(1*6)=96
96 % 10 = 6
So 765-86-6 is a valid CAS Registry Number.
765-86-6Relevant academic research and scientific papers
Ene Reactions of Conjugated Dienes. 2. Dependence of Rate on Degree of Hydrogen Removed and s-Cis or s-Trans Diene Character
Jacobson, Barry M.,Arvanitis, Georgia M.,Eliasen, Carol A.,Mitelman, Rimma
, p. 194 - 201 (2007/10/02)
The rates of the ene reactions between diethyl diazenedicarboxylate and a number of dienes have been measured and product structures determined.Accelerated reactions are observed with 1,3-cyclohexadienes but not with dienes held fixed in the s-trans form.Within the first set of systems tertiary hydrogens are much more reactive than secondary.Within the second set secondary are (in turn) more reactive than primary.There is no apparent correlation between the rate of the Diels-Alder reaction of the 1,3-cyclohexadienes with maleic anhydride and the rate of ene reaction with the diazenedicarboxylate.
