817-60-7

Basic information

• Product Name: 2-ethylheptan-1-ol
• Synonyms: 2-ethylheptan-1-ol;Einecs 212-444-4
• CAS NO: 817-60-7
• Molecular Formula: C₉H₂₀O
• Molecular Weight: 144.2545
• EINECS: 212-444-4
• Mol File: 817-60-7.mol
• Article Data: 6

Chemical Properties

• Melting Point: 6.15°C (estimate)
• Boiling Point: 192.9°C (estimate)
• Flash Point: 79.5°C
• Appearance: /
• Density: 0.8446 (estimate)
• Vapor Pressure: 0.102mmHg at 25°C
• Refractive Index: 1.4301
• CAS DataBase Reference: 2-ethylheptan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ethylheptan-1-ol(817-60-7)
• EPA Substance Registry System: 2-ethylheptan-1-ol(817-60-7)

Safety Data

• Hazardous Substances Data: 817-60-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H20O/c1-3-5-6-7-9(4-2)8-10/h9-10H,3-8H2,1-2H3

Upstream product

• 16429-10-0 3,6-diethyltetrahydro-2H-pyran-2-one 
• 111-67-1 2-octene 
• 201230-82-2 carbon monoxide 
• 111-66-0 oct-1-ene 
• 110-62-3 pentanal 
• 123-72-8 butyraldehyde 
• 13389-42-9 trans-2-Octene 
• 592-76-7 1-Heptene 
• 97-93-8 triethylaluminum 
• 74888-97-4 3-ethyl-5-prop-(E)-ylidene-5H-furan-2-one 
• 74888-93-0 (E)-3-ethylidene-6-vinyltetrahydro-2H-pyran-2-one 
• 484682-14-6 2-ethylheptan-4-olide 
• 50-00-0 formaldehyd 
• 1632-16-2 2-ethyl-1-hexene 

Downstream Products

• 27649-40-7 2-ethylheptanal 
• 3274-29-1 2-ethylheptanoic acid 

Relevant articles and documents

Iridium-Catalyzed Domino Hydroformylation/Hydrogenation of Olefins to Alcohols: Synergy of Two Ligands

A novel one-pot iridium-catalyzed domino hydroxymethylation of olefins, which relies on using two different ligands at the same time, is reported. DFT computation reveals different activities for the individual hydroformylation and hydrogenation steps in the presence of mono- and bidentate ligands. Whereas bidentate ligands have higher hydrogenation activity, monodentate ligands show higher hydroformylation activity. Accordingly, a catalyst system is introduced that uses dual ligands in the whole domino process. Control experiments show that the overall selectivity is kinetically controlled. Both computation and experiment explain the function of the two optimized ligands during the domino process.

From alkenes to alcohols by cobalt-catalyzed hydroformylation-reduction

The cobalt-catalyzed hydroformylation of alkenes in the presence of a range of novel cyclic phosphine ligands was investigated. The effect of various parameters such as solvents, additives, cobalt/phosphine ratio, CO/H2 (1:2), and nature of the alkenes was examined. The results revealed that both terminal and internal alkenes are hydroformylated in high yields to give mainly linear products at moderate temperature and syn gas pressure. The linearity ranges from 43 to 85%, with Lim-10 giving the highest proportion of linear product.

From olefins to alcohols: Efficient and regioselective ruthenium-catalyzed domino hydroformylation/reduction sequence

Exploring the alternatives: Ruthenium imidazoyl phosphine complexes catalyze the domino hydroformylation/reduction of alkenes to alcohols in good yields and with good selectivities (see scheme). Linear aliphatic alcohols are synthesized under reaction conditions typically used in industrial hydroformylations. Copyright