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
Enantioselective total synthesis of eudesma-3,11(13)-dien-12-oic acid
Chen,Zhou,Liu,Xiong,Li
, p. 1305 - 1307 (2007/10/03)
The first enantioselective total synthesis of eudesma-3,11(13)-dien-12-oic acid 1 was achieved starting from (+)-dihydrocarvone in ten steps.