1235-78-5 Usage
Uses
Used in Pharmaceutical Industry:
(2R)-3,3'aβ,6',6',9'aβ-Pentamethyl-3'a,4',5',5'aα,6',7',8',9',9'a,9'bα-decahydrospiro[furan-2(5H),2'(1'H)-naphtho[2,1-b]furan]-5-one is used as a pharmaceutical candidate for [application reason] due to its unique molecular structure and potential biological activity.
Used in Chemical Research:
In the field of chemical research, (2R)-3,3'aβ,6',6',9'aβ-Pentamethyl-3'a,4',5',5'aα,6',7',8',9',9'a,9'bα-decahydrospiro[furan-2(5H),2'(1'H)-naphtho[2,1-b]furan]-5-one serves as a subject of study for exploring new synthetic pathways, understanding its reactivity, and discovering novel applications based on its chemical properties.
Used in Material Science:
(2R)-3,3'aβ,6',6',9'aβ-Pentamethyl-3'a,4',5',5'aα,6',7',8',9',9'a,9'bα-decahydrospiro[furan-2(5H),2'(1'H)-naphtho[2,1-b]furan]-5-one is utilized in material science for the development of new materials with specific properties, such as high thermal stability, unique electronic characteristics, or specific optical properties, owing to its complex molecular architecture.
Check Digit Verification of cas no
The CAS Registry Mumber 1235-78-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1235-78:
(6*1)+(5*2)+(4*3)+(3*5)+(2*7)+(1*8)=65
65 % 10 = 5
So 1235-78-5 is a valid CAS Registry Number.
1235-78-5Relevant academic research and scientific papers
Chemistry of labdanediol from Cistus ladaniferus, L. synthesis of 12-Nor-ambreinolide and α and β-levantenolides
Urones,Basabe,Marcos,Diez Martin,Sexmero,Peral,Broughton
, p. 10389 - 10398 (2007/10/02)
Labdanediol, 2, the major component of the neutral part of Cistus ladaniferus L, was transformed into 12-nor-ambreinolide, precursor of ambrox, in three steps with an overall yield of 70%. Molecular modelling techniques have been used to determine the stereochemistry of the byproducts of these reactions. The selenylation and elimination reactions of α and βlevantanolides, obtained from labdanediol, 2, were used to synthetise α and β-levantenolides.
