77096-82-3 Usage
Description
(1S,8aβ)-Decahydro-5α-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aα-dimethyl-6-methylene-1-naphthalenecarboxylic acid is a complex carboxylic acid derivative of naphthalene, a polycyclic aromatic hydrocarbon. It features a hydroxy group, a methyl group, and a double bond in its structure, which contributes to its high reactivity and potential utility in various chemical reactions. The carboxylic acid group also allows it to engage in acid-base reactions and form salts. This chemical compound holds promise for a range of applications across different industries, pharmaceuticals, and research due to its intricate structure and reactivity.
Uses
Used in Chemical Synthesis:
(1S,8aβ)-Decahydro-5α-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aα-dimethyl-6-methylene-1-naphthalenecarboxylic acid is used as a key intermediate in the synthesis of various complex organic compounds. Its reactivity and structural features make it a valuable building block for creating pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (1S,8aβ)-Decahydro-5α-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aα-dimethyl-6-methylene-1-naphthalenecarboxylic acid is used as a precursor for the development of new drugs. Its unique structure can be leveraged to design molecules with specific biological activities, potentially leading to the creation of novel therapeutic agents.
Used in Material Science:
(1S,8aβ)-Decahydro-5α-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aα-dimethyl-6-methylene-1-naphthalenecarboxylic acid is utilized in material science for the development of new polymers and materials with tailored properties. Its ability to participate in acid-base reactions and form salts can contribute to the creation of materials with improved strength, stability, or other desirable characteristics.
Used in Research Applications:
In research settings, (1S,8aβ)-Decahydro-5α-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aα-dimethyl-6-methylene-1-naphthalenecarboxylic acid serves as a model compound for studying the reactivity and behavior of complex organic molecules. It can be used to explore reaction mechanisms, develop new synthetic methods, and understand the properties of related compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 77096-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,9 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77096-82:
(7*7)+(6*7)+(5*0)+(4*9)+(3*6)+(2*8)+(1*2)=163
163 % 10 = 3
So 77096-82-3 is a valid CAS Registry Number.
77096-82-3Relevant articles and documents
LABDANES FROM CRYPTOMERIA JAPONICA
Su, Wen-Chiung,Fang, Jim-Min,Cheng, Yu-Shia
, p. 1109 - 1114 (2007/10/02)
Twenty-seven labdanes were isolated from the leaves of Cryptomeria japonica.The new compounds include 15-(2-oxopropylidene)labd-8(17)-en-19-oic acid, 15-oxolabda-8(17),13(E)-dien-19-oic acid, 7β-acetoxy-15-hydroxylabda-8(17),13E-dien-19-oic acid methyl ester, 14-hydroxy-15-norlabd-8(17)-en-19-oic acid methyl ester, 15-hydroxylabda-8(17),13Z-dien-19-oic acid methyl ester, 15,16-epoxylabda-13(16),14-dien-8α,19-diol, 8α-hydroxylabda-13(16),14-dien-19-yl p-methoxycinnamate, an ester formed by 15-acetylisocupressic acid and cryptomeridiol and an ether formed by isocupressic acid and cryptomeridiol. - Key words: Cryptomeria japonica; Taxodiaceae; leaves; diterpenes; labdane-type.
