6090-15-9

Basic information

• Product Name: 2,6-DIMETHYL-5-HEPTEN-2-OL
• Synonyms: 2,6-dimethyl-2-hepten-6-ol;2,6-DIMETHYL-5-HEPTEN-2-OL;2,6-DIMETHYL-5-HEPTENE-2-OL;2,6-dimethylhept-5-en-2-ol;5-Hepten-2-ol, 2,6-dimethyl-;DIMETHYL-(2,6)-HEPTEN-(5)-OL-(2);Ai3-38066;Einecs 228-029-6
• CAS NO: 6090-15-9
• Molecular Formula: C₉H₁₈O
• Molecular Weight: 142.24
• EINECS: 228-029-6
• Mol File: 6090-15-9.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 203.2 °C at 760 mmHg
• Flash Point: 90.1 °C
• Appearance: /
• Density: 0.846 g/cm³
• Vapor Pressure: 0.0683mmHg at 25°C
• Refractive Index: 1.449
• CAS DataBase Reference: 2,6-DIMETHYL-5-HEPTEN-2-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIMETHYL-5-HEPTEN-2-OL(6090-15-9)
• EPA Substance Registry System: 2,6-DIMETHYL-5-HEPTEN-2-OL(6090-15-9)

Safety Data

• Hazardous Substances Data: 6090-15-9(Hazardous Substances Data)

Usage

General Description

2,6-DIMETHYL-5-HEPTEN-2-OL is a chemical compound with the molecular formula C9H18O. It is a colorless liquid with a strong, sweet odor. It is commonly used as a flavor and fragrance ingredient in the food and cosmetic industry. It is also known for its insect repellent properties and is used in insect repellent products. Additionally, it has been studied for its potential antimicrobial and antifungal properties. 2,6-DIMETHYL-5-HEPTEN-2-OL is considered to be relatively safe for use and is generally recognized as safe (GRAS) for use in food products.

InChI:InChI=1/C9H18O/c1-8(2)6-5-7-9(3,4)10/h6,10H,5,7H2,1-4H3

Upstream product

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Downstream Products

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• 3123-97-5 dihydro-5,5-dimethyl-2(3H)-furanone 
• 6090-16-0 2,6-dimethyl-2,5-heptadiene 
• 64-19-7 acetic acid 
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Relevant articles and documents

Intramolecular hydroalkoxylation catalyzed inside a self-assembled cavity of an enzyme-like host structure

Self-assembled resorcin[4]arene hexamer catalyzes the intramolecular hydroalkoxylation of unsaturated alcohols to the corresponding cyclic ethers under mild conditions. The mode of catalysis and encapsulation-based substrate selectivity of the host efficiently mimic the basic principle of operation observed in enzymes.

Organocatalysis in a synthetic receptor with an inwardly directed carboxylic acid

A cavitand functionalized with a Kemp-s triacid derivative was used to catalyze the epoxide ring-opening cyclizations of 1,5-epoxyalcohols. A deep, cylindrical cavity containing electron-rich aromatic walls and an inwardly directed carboxylic acid displayed the necessary characteristics to bind different 1,5-epoxyalcohols and initiate their cyclization reactions. The reactions inside this synthetic receptor occurred in a catalytic and regioselective manner. These results highlight that the arrangement of functionality and unique solvation provided by the structured interiors of natural enzymes can be incorporated into synthetic systems having useful physical and chemical properties. Copyright

SUBSTITUENT-DIRECTED OXIDATIVE CYCLIZATION OF γ-HYDROXY OLEFINS TO γ-LACTONES WITH HEXAVALENT OXO-CHROMIUM REAGENTS

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