41370-29-0

Basic information

• Product Name: 2-(3,3-dimethylcyclohexylidene)ethanol
• Synonyms: 2-(3,3-dimethylcyclohexylidene)ethanol
• CAS NO: 41370-29-0
• Molecular Formula: C10H18O
• Molecular Weight: 154.24932
• EINECS: 255-336-2
• Mol File: 41370-29-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 212.7°Cat760mmHg
• Flash Point: 90°C
• Appearance: /
• Density: 0.966g/cm³
• Vapor Pressure: 0.0382mmHg at 25°C
• Refractive Index: 1.531
• CAS DataBase Reference: 2-(3,3-dimethylcyclohexylidene)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,3-dimethylcyclohexylidene)ethanol(41370-29-0)
• EPA Substance Registry System: 2-(3,3-dimethylcyclohexylidene)ethanol(41370-29-0)

Safety Data

• Hazardous Substances Data: 41370-29-0(Hazardous Substances Data)

Usage

Color

Colorless

Physical state

Liquid

Uses

Building block in the synthesis of various organic compounds, production of fragrances, flavorings, and pharmaceuticals, solvent, intermediate in the manufacturing of other chemical products

Unique properties

Unique chemical structure

Versatility

Wide range of applications in the chemical industry.

InChI:InChI=1/C10H18O/c1-10(2)6-3-4-9(8-10)5-7-11/h5,11H,3-4,6-8H2,1-2H3

Upstream product

• 121617-98-9 (Z)-2-ochtoden-1-ol tetrahydropyranyl ether 
• 116440-82-5 tert-Butyl-{2-[3,3-dimethyl-cyclohex-(E)-ylidene]-ethoxy}-dimethyl-silane 
• 82528-39-0 6-phenylthio-2-ochtoden-1-ol 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 5629-80-1 (1-hydroxy-3,3-dimethyl-cyclohexyl)-acetic acid ethyl ester 
• 30346-22-6 3,3-Dimethyl-1-hydroxy-cyclohexylessigsaeure 
• 112381-71-2 (E)-8-Iodo-7,7-dimethyl-3-tributylstannanyl-oct-2-enoic acid methyl ester 
• 82528-38-9 1-acetoxy-6-phenylthio-2-ochtodene 
• 82528-40-3 (EZ)-6-hydroxy-2-ochtoden-1-yl trifluoroacetate 
• 82528-37-8 1-chloro-6-phenylthio-2-ochtodene 
• 70473-42-6 [1-(1-Chloro-1-methyl-ethyl)-4-methylene-hex-5-enylsulfanyl]-benzene 
• 123-35-3 7-methyl-3-methene-1,6-octadiene 
• 116440-76-7 5,5-Dimethyl-oct-7-en-2-yn-1-ol 
• 116440-79-0 ((Z)-8-Bromo-3-iodo-5,5-dimethyl-oct-2-enyloxy)-tert-butyl-dimethyl-silane 

Downstream Products

• 20489-81-0 5-(3,3-dimethyl-cyclohexylidene)-pent-3-en-2-one 

Relevant articles and documents

Pheromone Synthesis, CXV. - Synthesis of (Z)-2-Ochtoden-1-ol, (E)-2-Ochtoden-1-al, and (Z)-2-Ochtoden-1-al, the Pheromone Components of the Boll Weevil (Anthonomus grandis)

The synthesis of geometrically pure (Z)-2-ochtoden-1-ol (1), (E)-2-ochtoden-1-al (2), and (Z)-2-ochtoden-1-al (3) was achieved starting from myrcene.

THE STEREOSPECIFIC FORMATION OF AN EXOCYCLIC ALKENE BY A CONSECUTIVE RADICAL CYCLIZATION-ELEIMINATION

The iodovinylstannanes 4 and 5 were prepared by the conjugate addition of the tri-n-butyltin moiety to a substituted propiolic ester.Compounds 4 and 5 underwent a radical cyclization-elimination reaction to stereospecifically generate an exocyclic alkene.

NEW OCHTODANE SYNTHESES FROM MYRCENE

The ochtodane skeleton is formed stereoselectively from myrcene via acid-catalyzed cyclization of the benzenesulfenyl chloride adduct and the epoxide in a biogenetic type fashion.Its application to the syntheses of two ochtodane-type monoterpenes, an aldehyde component of the boll weevil pheromone and a diol found in the red alga Ochtodes crockeri, is reported.