4117-14-0

Basic information

• Product Name: 2-Decyn-1-ol
• Synonyms: 2-Decyne-1-ol;N-HEPTYLHYDROXYMETHYLACETYLENE;TIMTEC-BB SBB008898;2-DECYN-1-OL;Decynol;Dec-2-yn-1-ol;2-DECYN-1-OL 97%;Heptyl(hydroxymethyl)acetylene
• CAS NO: 4117-14-0
• Molecular Formula: C₁₀H₁₈O
• Molecular Weight: 154.25
• Product Categories: Acetylenes;Acetylenic Alcohols & Their Derivatives;Alkynes;Internal;Organic Building Blocks
• Mol File: 4117-14-0.mol
• Article Data: 29

Chemical Properties

• Melting Point: 1.9°C (estimate)
• Boiling Point: 70-74°C 0,01mm
• Flash Point: 114-116°C/6mm
• Appearance: /
• Density: 0.855
• Vapor Pressure: 0.482mmHg at 25°C
• Refractive Index: 1.4585
• Storage Temp.: 2-8°C
• Solubility: Chloroform, Ethyl Acetate
• PKA: 13.01±0.10(Predicted)
• BRN: 1852842
• CAS DataBase Reference: 2-Decyn-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Decyn-1-ol(4117-14-0)
• EPA Substance Registry System: 2-Decyn-1-ol(4117-14-0)

Safety Data

• Safety Statements: 23-24/25
• WGK Germany: 3
• Hazardous Substances Data: 4117-14-0(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 4117-14-0 differently. You can refer to the following data:
1. 2-Decyn-1-ol is used in the synthesis of antitumor agents, isomers of Panaxytriol and Falcarinol (F101100). Also used in the synthesis of aromatase inhibitors used in the treatment of cancers, primari ly breast and ovarian.
2. 2-Decyn-1-ol is used in the synthesis of antitumor agents, isomers of Panaxytriol and Falcarinol (F101100). Also used in the synthesis of aromatase inhibitors used in the treatment of cancers, primarily breast and ovarian.

InChI:InChI=1/C10H18O/c1-2-3-4-5-6-7-8-9-10-11/h11H,2-7,10H2,1H3

Upstream product

• 629-04-9 1-Bromoheptane 
• 6089-04-9 3-(tetrahydropyran-2'-yloxy)propyne 
• 50-00-0 formaldehyd 
• 3452-09-3 1-nonyne 
• 4282-40-0 1-Iodoheptane 
• 88517-98-0 2-Decyl-1-ol THP ether 
• 107-19-7 propargyl alcohol 
• 68274-97-5 dec-5-yn-1-ol 

Downstream Products

• 18409-18-2 (E)-2-decenol 
• 4194-71-2 (Z)-2-decen-1-ol 
• 3913-81-3 (E)-2-decenal 
• 2497-25-8 (Z)‐dec‐2‐enal 
• 51721-39-2 3-decyn-1-ol 
• 69222-06-6 4-decyne-1-ol 
• 68274-97-5 dec-5-yn-1-ol 
• 69222-07-7 dec-6-yn-1-ol 
• 69222-08-8 7-decyn-1-ol 
• 17643-36-6 9-decyn-1-ol 
• 228403-27-8 C₂₀H₂₈O₃ 
• 326593-57-1 C₄₀H₅₄O₆ 
• 228403-32-5 C₄₀H₅₈O₆ 
• 326593-58-2 C₆₀H₉₀O₆ 

Relevant articles and documents

Sex attractants of geometrid and noctuid moths: Chemical characterization and field test of monoepoxides of 6,9-dienes and related compounds

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Total syntheses of 9-epoxyfalcarindiol and its diastereomer

The first total syntheses of 9-epoxyfalcarindiol 1a and its diastereomer 1b have been achieved. Central to our approach were the Zn-cyclopropane-based amino alcohol catalyzed enantioselective alkynylation of acrolein, the diastereoselective addition of a diynic ester to an epoxy aldehyde, and the asymmetric Sharpless epoxidation of allylic alcohol catalyzed with L-(+)-diethyl tartrate and Ti(OiPr)4.

Tetris in monolayers: Patterned self-assembly using side chain shape

The "kinked" shapes of conjugated alkadiynes constrain chain packing in monolayers on HOPG. Centrally located diyne units permit assembly of 1,5-bis(alkadiyne)anthracene monolayers. Off-center diynes inhibit self-assembly. Shape matched pairs of off-center diyne chains direct self-assembly of compositionally patterned, two component monolayers.