1259-94-5 Usage
General Description
1-(4-Isopropyl-1-methyl-4-pentenyl)-3a,6,6,12a-tetramethyltetradecahyd ro-1H-cyclopenta[a]cyclopropa[e]phenanthren-7-yl acetate is a complex chemical compound that falls under the category of cyclopropylphenanthrene derivatives. 1-(4-Isopropyl-1-methyl-4-pentenyl)-3a,6,6,12a-tetramethyltetradecahyd ro-1H-cyclopenta[a]cyclopropa[e]phenanthren-7-yl acetate is an acetate ester that contains a cyclopenta[a]cyclopropa[e]phenanthrene core structure, which is a type of polycyclic hydrocarbon. It also contains isopropyl, methyl, and pentenyl functional groups. Its chemical structure is characterized by multiple methyl and hydrogen substituents. 1-(4-Isopropyl-1-methyl-4-pentenyl)-3a,6,6,12a-tetramethyltetradecahyd ro-1H-cyclopenta[a]cyclopropa[e]phenanthren-7-yl acetate may have potential applications in the fields of chemistry, pharmaceuticals, and materials science, although further research would be needed to fully understand its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 1259-94-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,5 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1259-94:
(6*1)+(5*2)+(4*5)+(3*9)+(2*9)+(1*4)=85
85 % 10 = 5
So 1259-94-5 is a valid CAS Registry Number.
1259-94-5Relevant articles and documents
Conformational Analysis of Cycloartenol, 24-Methylenecycloartanol and Their Derivatives
Yoshida, Kumi,Hirose, Yoshihiko,Imai, Yutaka,Kondo, Tadao
, p. 1901 - 1912 (2007/10/02)
A conformational analysis of cycloartenol, 24-methylenecycloartenol and their derivatives was carried out in the solution and the solid state by an NMR study and X-ray crystallographic analysis, respectively.Complete assignments of the 1H NMR spectra of these compounds were made in order to elucidate the conformation involving the ring system and side chain.Rings A to C had a chair-halfchair-boat conformation, and the side chain had a zig-zag conformation.
