28399-17-9 Usage
Description
2-[(2R,4aR,8aR)-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-2-yl]prop-2-enoic acid is a bicyclic organic compound derived from octahydronaphthalene. It features a propenoic acid group attached to a naphthalene ring system, which endows it with unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Synthesis:
2-[(2R,4aR,8aR)-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-2-yl]prop-2-enoic acid is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the development of complex organic molecules with potential therapeutic effects.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2-[(2R,4aR,8aR)-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-2-yl]prop-2-enoic acid serves as a key intermediate in the creation of compounds with pesticidal or herbicidal properties, contributing to the development of effective crop protection agents.
Used in Organic Chemistry Research:
2-[(2R,4aR,8aR)-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-2-yl]prop-2-enoic acid is utilized in the field of organic chemistry for the exploration and development of new synthetic methods and strategies. Its distinctive structure provides a platform for advancing the understanding of organic reactions and the creation of innovative synthetic pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 28399-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,9 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28399-17:
(7*2)+(6*8)+(5*3)+(4*9)+(3*9)+(2*1)+(1*7)=149
149 % 10 = 9
So 28399-17-9 is a valid CAS Registry Number.
28399-17-9Relevant articles and documents
Germacrenes from fresh costus roots
De Kraker, Jan-Willem,Franssen, Maurice C.R,De Groot, Aede,Shibata, Toshiro,Bouwmeester, Harro J
, p. 481 - 487 (2007/10/03)
Four germacrenes, previously shown to be intermediates in sesquiterpene lactone biosynthesis, were isolated from fresh costus roots (Saussurea lappa). The structures of (+)-germacrene A, germacra-1(10),4,11(13)-trien-12-ol, germacra-1(10),4,11(13)-trien-12-al, and germacra-1(10),4,11(13)-trien-12-oic acid were deduced by a combination of spectral data and chemical transformations. Heating of these compounds yields (-)-β-elemene, (-)-elema-1,3,11(13)-trien-12-ol, (-)-elema-1,3,11(13)-trien-12-al, and elema-1,3,11(13)-trien12-oic acid respectively, in addition to small amounts of their diastereomers. Acid induced cyclisation of the germacrenes yields selinene, costol, costal, and costic acid respectively. It is highly probable that the elemenes reported in literature for costus root oil are artefacts.
