90332-93-7 Usage
Description
(4aR)-4,4aα,5,6,7,8,8a,9-Octahydro-3,5,8aβ-trimethylnaphtho[2,3-b]furan-5α-ol, also known as 4,4aα,5,6,7,8,8a,9-octahydro-3,5,8aβ-trimethylnaphtho[2,3-b]furan-5α-ol, is a complex organic compound belonging to the naphthofuran class. It features a naphthalene backbone fused with a furan ring and an octahydro-prenylated furan moiety. As an alcohol derivative, it exhibits unique stereochemistry, denoted by the (4aR) and 5α-ol components in its name. With a molecular formula of C15H24O, this chemical may hold promise in organic synthesis and medicinal chemistry due to its intricate structure and potential biological properties.
Uses
Used in Organic Synthesis:
(4aR)-4,4aα,5,6,7,8,8a,9-Octahydro-3,5,8aβ-trimethylnaphtho[2,3-b]furan-5α-ol is utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure and functional groups make it a valuable building block for developing new compounds with specific properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4aR)-4,4aα,5,6,7,8,8a,9-Octahydro-3,5,8aβ-trimethylnaphtho[2,3-b]furan-5α-ol serves as a potential candidate for drug discovery. Its complex structure and stereochemistry may contribute to the development of novel therapeutic agents with specific biological activities, targeting a range of diseases and conditions.
Used in Pharmaceutical Industry:
(4aR)-4,4aα,5,6,7,8,8a,9-Octahydro-3,5,8aβ-trimethylnaphtho[2,3-b]furan-5α-ol is employed as a starting material or a component in the synthesis of pharmaceutical compounds. Its unique features can be leveraged to design and develop innovative drugs with improved efficacy and selectivity.
Used in Research and Development:
This naphthofuran compound is also used in research and development settings to explore its chemical properties, reactivity, and potential interactions with biological systems. Understanding its behavior can lead to new insights and applications in both academia and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 90332-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,3 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90332-93:
(7*9)+(6*0)+(5*3)+(4*3)+(3*2)+(2*9)+(1*3)=117
117 % 10 = 7
So 90332-93-7 is a valid CAS Registry Number.
90332-93-7Relevant articles and documents
Structures of Novel Sesquiterpene Alcohols from Chloranthus japonicus (Chloranthaceae)
Kawabata, Jun,Fukushi, Yukiharu,Tahara, Satoshi,Mizutani, Junya
, p. 713 - 718 (2007/10/02)
Tree novel sesquiterpene alcohols, shizuka-acoradienol (2), shizukafuranol (3) and shizukolidol (4), were isolated from Chloranthus japonicus Sieb. (Japanese name: Hitori-shizuka, Chloranthaceae).Their structures were elucidated on the basis of their physicochemical properties and some chemical reactions.Furanodienone (5), scopoletin (6a) and isoscopoletin (6b) were also isolated from this plant.
