40575-42-6

Basic information

• Product Name: 1-OCTEN-4-OL
• Synonyms: 1-OCTEN-4-OL;Allyl n-butyl carbinol;1-Octen-4-ol,99%;oct-1-en-4-ol;1-OCTEN-4-OL, 98%,
• CAS NO: 40575-42-6
• Molecular Formula: C₈H₁₆O
• Molecular Weight: 128.21
• Mol File: 40575-42-6.mol
• Article Data: 30

Chemical Properties

• Melting Point: -31.5°C (estimate)
• Boiling Point: 202.67°C (estimate)
• Flash Point: 67.2 °C
• Appearance: /
• Density: 0,83 g/cm3
• Vapor Pressure: 0.286mmHg at 25°C
• Refractive Index: 1.4359 (estimate)
• CAS DataBase Reference: 1-OCTEN-4-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 1-OCTEN-4-OL(40575-42-6)
• EPA Substance Registry System: 1-OCTEN-4-OL(40575-42-6)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 40575-42-6(Hazardous Substances Data)

Usage

General Description

1-Octen-4-ol, also known as mushroom alcohol, is a volatile organic compound with a strong, unpleasant odor reminiscent of fungus or mildew. It is commonly found in mushrooms, and is produced by the decomposition of plant material. This chemical has been identified as a major component of the characteristic aroma of white truffles, and is also a key contributor to the earthy and musty smell of mold. In addition to its role in natural environments, 1-Octen-4-ol is used in the fragrance industry to impart a musty, mushroom-like note to perfumes, as well as in insect attractant formulations to lure pests such as mosquitoes and houseflies. Its unique odor profile and potential applications make it an interesting and versatile chemical compound with diverse uses across different industries.

InChI:InChI=1/C8H16O/c1-3-5-7-8(9)6-4-2/h4,8-9H,2-3,5-7H2,1H3/t8-/m1/s1

Upstream product

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Downstream Products

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Relevant articles and documents

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An efficient synthesis of α,β-unsaturated alkylimines at low temperature using azides has been developed. Carbocations generated from allyl alcohols helped achieve a rapid conversion under mild conditions with azides to afford reactive α,β-unsaturated imines. Hydroxy or alkoxy groups are essential for these transformations, and utilizing readily accessible allyl alcohols gave a wide extension of substrates. The efficiency of this novel method is demonstrated in the total synthesis of an iminium ant venom alkaloid.