511-59-1 Usage
Description
(1S-exo)-2-methyl-3-methylene-2-(4-methyl-3-pentenyl)bicyclo[2.2.1]heptane is a sesquiterpene and carbobicyclic compound with the chemical structure of bicyclo[2.2.1]heptane. It has a methylidene group at position 3, and the 2-exoand 2-endohydrogens are substituted by 2-methylpent-en-5-yl and methyl groups, respectively. (1S-exo)-2-methyl-3-methylene-2-(4-methyl-3-pentenyl)bicyclo[2.2.1]heptane is specifically the 1S,2R,4R enantiomer.
Uses
Used in Pharmaceutical Industry:
(1S-exo)-2-methyl-3-methylene-2-(4-methyl-3-pentenyl)bicyclo[2.2.1]heptane is used as a pharmaceutical compound for its potential therapeutic properties. Its unique chemical structure allows it to interact with biological targets and modulate various biological pathways, making it a promising candidate for the development of new drugs.
Used in Fragrance Industry:
(1S-exo)-2-methyl-3-methylene-2-(4-methyl-3-pentenyl)bicyclo[2.2.1]heptane is used as a fragrance ingredient due to its unique and pleasant aroma. Its ability to create a distinct scent profile makes it valuable in the formulation of perfumes, colognes, and other fragrance products.
Used in Flavor Industry:
(1S-exo)-2-methyl-3-methylene-2-(4-methyl-3-pentenyl)bicyclo[2.2.1]heptane is used as a flavoring agent in the food and beverage industry. Its unique taste profile can enhance the flavor of various products, making it a valuable ingredient in the creation of new and innovative flavors.
Used in Agrochemical Industry:
(1S-exo)-2-methyl-3-methylene-2-(4-methyl-3-pentenyl)bicyclo[2.2.1]heptane is used as an agrochemical compound for its potential applications in pest control and crop protection. Its unique chemical structure allows it to target specific pests and diseases, making it a valuable tool in the development of new and effective agrochemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 511-59-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 511-59:
(5*5)+(4*1)+(3*1)+(2*5)+(1*9)=51
51 % 10 = 1
So 511-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H24/c1-11(2)6-5-9-15(4)12(3)13-7-8-14(15)10-13/h6,13-14H,3,5,7-10H2,1-2,4H3
511-59-1Relevant articles and documents
A SESQUITERPENOID ANT REPELLENT FROM DYSOXYLUM SPECTABILE
Russell, Graeme B.,Hunt, Martin B.,Bowers, William S.,Blunt, John B.
, p. 1455 - 1456 (1994)
(2S,3R)-2,3-Dimethyl-3-(4-methyl-3-pentenyl)-2-norbornanol was isolated as the ant repellent in an activity guided separation of the fruits of Dysoxylum spectabile.The structure of the alcohol was established by NMR.Other sesquiterpenes were recognized in a GCMS analysis of the steam distillate.
Syntheses of epi-β-santalene, β-santalene and an isomer of β-santalene with 4-methyl-4-pentenyl side chain
Unnikrishnan,Vatakencherry
, p. 3159 - 3168 (2007/10/02)
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Total Syntheses of Sandalwood Fragrances: (Z)- and (E)-β-Santalol and Their Enantiomers, ent-β-Santalene
Krotz, Achim,Helmchen, Guenter
, p. 537 - 540 (2007/10/02)
Via asymmetric Diels-Alder reactions, large scale preparations of enantiomerically pure norbornane-2-carboxylic acids were carried out.Oxidative degradation furnished 2-norbornanone and 3-methyl-2-norbornanone which gave the title compounds via stereoselective alkylations, subsequent Wittig reactions and reductions.