62108-07-0

Basic information

• Product Name: 4-N-PROPYL-1-HEPTEN-4-OL
• Synonyms: 4-PROPYL-1-HEPTEN-4-OL;4-N-PROPYL-1-HEPTEN-4-OL;4-propylhept-1-en-4-ol;Allyl di-n-propyl carbinol
• CAS NO: 62108-07-0
• Molecular Formula: C₁₀H₂₀O
• Molecular Weight: 156.27
• EINECS: 263-409-5
• Mol File: 62108-07-0.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 215.7°Cat760mmHg
• Flash Point: 84.7°C
• Appearance: /
• Density: 0.839g/cm³
• Vapor Pressure: 0.0316mmHg at 25°C
• Refractive Index: 1.445
• PKA: 15.17±0.29(Predicted)
• CAS DataBase Reference: 4-N-PROPYL-1-HEPTEN-4-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-N-PROPYL-1-HEPTEN-4-OL(62108-07-0)
• EPA Substance Registry System: 4-N-PROPYL-1-HEPTEN-4-OL(62108-07-0)

Safety Data

• Hazardous Substances Data: 62108-07-0(Hazardous Substances Data)

Usage

General Description

4-N-PROPYL-1-HEPTEN-4-OL is a chemical compound that belongs to the class of alcohols. It is also known as phebol and has a molecular formula of C10H20O. 4-N-PROPYL-1-HEPTEN-4-OL is a colorless liquid with a fruity odor and is commonly used in the production of perfumes and flavorings. It is also used as a fragrance ingredient in a variety of personal care products and cosmetics. Additionally, 4-N-PROPYL-1-HEPTEN-4-OL has potential antimicrobial and antioxidant properties, making it a valuable ingredient in some pharmaceutical and food applications.

InChI:InChI=1/C10H20O/c1-4-7-10(11,8-5-2)9-6-3/h4,11H,1,5-9H2,2-3H3

Upstream product

• 123-19-3 4-heptanone 
• 106-95-6 allyl bromide 
• 1730-25-2 allylmagnesium bromide 
• 10152-76-8 allylmethyl sulfide 
• 101536-69-0 2-Chloro-4-propyl-heptan-4-ol 
• 2622-05-1 allylmagnesium bromide 
• 108-94-1 cyclohexanone 
• 75863-14-8 2-Propenyltitanium triisopropoxide 
• 110-43-0 n-pentyl methyl ketone 
• 24850-33-7 allyltributylstanane 
• 556-56-9 allyl iodid 

Downstream Products

• 23985-60-6 3-hydroxy-3-propyl-hexanoic acid 
• 144-62-7 oxalic acid 
• 123-19-3 4-heptanone 
• 124-38-9 carbon dioxide 
• 802294-64-0 propionic acid 
• 107-92-6 butyric acid 
• 79874-76-3 3-(4-propyl-heptyl)-4-(2-hydroxyethyl)-morpholine 

Relevant articles and documents

METHODS OF MAKING DELMOPINOL AND SALTS THEREOF

Disclosed are methods of making delmopinol and delmopinol salts (e.g., delmopinol metal salts, such as, for example, delmopinol calcium salts, delmopinol sodium salts, delmopinol potassium salts, and/or delmopinol magnesium salts). Delmopinol has structure (I) and a salt of delmopinol has structure (II).

General, Auxiliary-Enabled Photoinduced Pd-Catalyzed Remote Desaturation of Aliphatic Alcohols

A general, efficient, and site-selective visible light-induced Pd-catalyzed remote desaturation of aliphatic alcohols into valuable allylic, homoallylic, and bis-homoallylic alcohols has been developed. This transformation operates via a hybrid Pd-radical mechanism, which synergistically combines the favorable features of radical approaches, such as a facile remote C-H HAT step, with that of transition-metal-catalyzed chemistry (selective β-hydrogen elimination step). This allows achieving superior degrees of regioselectivity and yields in the desaturation of alcohols compared to those obtained by the state-of-the-art desaturation methods. The HAT at unactivated C(sp3)-H sites is enabled by the easily installable/removable Si-auxiliaries. Formation of the key hybrid alkyl Pd-radical intermediates is efficiently induced by visible light from alkyl iodides and Pd(0) complexes. Notably, this method requires no exogenous photosensitizers or external oxidants.

Direct transformation of allylic and benzylic thiols, thioethers, and disulfides into organolithium compounds

The reaction of allylic and benzylic thiols 1, disulfides 3, and thioethers 4 and 5 with an excess of lithium and a catalytic amount of 4,4′-di-tert-butylbiphenyl (DTBB, 5mol%) afforded the corresponding allylic and benzylic organolithium reagents via reductive cleavage of the carbon-sulfur bond. The generated organolithium compounds gave the expected products 2 by reaction with several electrophiles followed by hydrolysis with water. The reaction conditions and the lithiation procedure (stepwise of Barbier-type process) depended on the starting sulfur containing compound.