64236-38-0 Usage
Uses
Used in Organic Chemistry:
(3R)-4α,4aα-Dimethyl-3β-hydroxy-1,2,3,4,4a,5,6,7-octahydro-6β-(2-propenyl)naphthalen-7-one is used as a building block for the synthesis of more complex organic molecules, leveraging its unique structure and functional groups for creating novel compounds with specific properties.
Used in Pharmaceutical Industry:
As a potential pharmaceutical intermediate, (3R)-4α,4aα-Dimethyl-3β-hydroxy-1,2,3,4,4a,5,6,7-octahydro-6β-(2-propenyl)naphthalen-7-one can be utilized in the development of new drugs, particularly those targeting specific biological pathways or receptors due to its structural features.
Used in Natural Product Synthesis:
(3R)-4α,4aα-Dimethyl-3β-hydroxy-1,2,3,4,4a,5,6,7-octahydro-6β-(2-propenyl)naphthalen-7-one is used as a key intermediate in the synthesis of natural products, contributing to the creation of bioactive molecules that can be found in plants, fungi, or other organisms, which may have medicinal or biological significance.
Further research is essential to explore the full potential of (3R)-4α,4aα-Dimethyl-3β-hydroxy-1,2,3,4,4a,5,6,7-octahydro-6β-(2-propenyl)naphthalen-7-one across different industries and applications, as its unique structure and properties may offer innovative solutions in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 64236-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,3 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64236-38:
(7*6)+(6*4)+(5*2)+(4*3)+(3*6)+(2*3)+(1*8)=120
120 % 10 = 0
So 64236-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O2/c1-9(2)12-8-15(4)10(3)13(16)6-5-11(15)7-14(12)17/h7,10,12-13,16H,1,5-6,8H2,2-4H3/t10-,12-,13+,15+/m0/s1
64236-38-0Relevant academic research and scientific papers
Bioactive sesquiterpene derivatives from mangrove endophytic fungus Phomopsis sp. SYSU-QYP-23: Structures and nitric oxide inhibitory activities
Chen, Yan,Liu, Hongju,Zou, Ge,Yang, Wencong,Zhang, Lishan,Yan, Zhangyuan,Long, Yuhua,She, Zhigang
, (2020/12/21)
Eight new sesquiterpene derivatives (2, 4–6 and 10–13), along with five known analogues were isolated from the mangrove endophytic fungus Phomopsis sp. SYSU-QYP-23. Their structures of new compounds were established by spectroscopic methods, and the absol
Homopetasinic acid isolated from Diaporthe sp. strain 1308-05
Ito, Atsushi,Kumagai, Ikuya,Maruyama, Miku,Maeda, Hayato,Tonouchi, Akio,Nehira, Tatsuo,Kimura, Ken-Ichi,Hashimoto, Masaru
supporting information, p. 1117 - 1119 (2016/03/09)
Homopetasinic acid (1) was isolated from fungi of the Diaporthe sp. strain 1308-05. NMR spectroscopic structural analysis revealed a petasol (3) substructure and a (4E,6E)-7-carboxy-3-hydroxy-2-methylhepta-4,6-dienoate side chain. The absolute configuration of the petasol moiety was established by the specific rotation value after basic hydrolysis. The (2′S,3′S)-configuration of the side chain was determined by NMR empirical methods as well as comparison of the spectral data with related model compounds. The absolute structure of the side chain moiety was established on the basis of ECD spectral analyses involving theoretical calculations. The biological activities of 1 are also discussed.
