61505-17-7 Usage
Description
(4R)-1,4-dimethyl-4-[(1R)-1-methyl-2-methylidenecyclopentyl]cyclohexene is a complex organic compound belonging to the class of cycloalkenes. It features a cyclohexene ring with two methyl groups at the 1 and 4 positions and a cyclopentyl group at the 2 position, with a (1R) configuration at the cyclopentyl group, reflecting its stereochemistry.
Uses
Used in Organic Chemistry Research:
(4R)-1,4-dimethyl-4-[(1R)-1-methyl-2-methylidenecyclopentyl]cyclohexene is utilized as a reference compound in the field of organic chemistry. Its unique structure and properties make it valuable for understanding various chemical reactions and mechanisms.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4R)-1,4-dimethyl-4-[(1R)-1-methyl-2-methylidenecyclopentyl]cyclohexene may have potential applications due to its complex structure and specific stereochemistry. It could be used as a starting material for the synthesis of new drugs or as a structural component in drug design.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, this compound might find use as a precursor for the development of new pesticides or other agrochemical products, taking advantage of its unique structural features.
Further research and study of (4R)-1,4-dimethyl-4-[(1R)-1-methyl-2-methylidenecyclopentyl]cyclohexene are necessary to fully understand its properties and explore additional potential uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 61505-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,0 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61505-17:
(7*6)+(6*1)+(5*5)+(4*0)+(3*5)+(2*1)+(1*7)=97
97 % 10 = 7
So 61505-17-7 is a valid CAS Registry Number.
61505-17-7Relevant articles and documents
Synthesis of the sesquiterpenoid trichodiene using a free radical fragmentation approach
Lange, Gordon L.,Furlan, Lorena,MacKinnon, Mark C.
, p. 5489 - 5492 (1998)
A highly regio- and stereoselective synthesis of the sesquiterpenoid trichodiene is reported. The approach requires only nine steps starting with a [2+2] photoaddition and employs the free radical fragmentation of an 'external' cyclobutane bond in a key step.
Stereoselective Synthesis of (+/-)-Trichodiene
Harding, Kenn E.,Clement, K. S.,Tseng, C.-Y.
, p. 4403 - 4410 (2007/10/02)
Details of a convergent stereoselective synthesis of trichodiene (1) from simple monocyclic starting materials are reported.Stereochemical control is effected by Nazarov cyclization of dienone 14 and C-C bond cleavage of the resulting tricyclic products 1
Trichothecine synthesis using organoiron complexes: Diastereoselective total syntheses of (±)-trichodiene, (±)-12,13-epoxytrichothec-9-ene, and (±)-trichodermol
Pearson,O'Brien
, p. 4663 - 4673 (2007/10/02)
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