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2-Hexyn-1-ol

  • CAS No.: 764-60-3
  • Purity: 99%
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Purity 99% Min 2-Hexyn-1-ol 764-60-3 Spot Supply with Safe Transportation

  • Molecular Formula: C6H10 O
  • Molecular Weight: 98.1448
  • Appearance/Colour: COLORLESS TO YELLOW LIQUID 
  • Vapor Pressure: 2.52mmHg at 25°C 
  • Melting Point: -52.5°C 
  • Refractive Index: n20/D 1.4536(lit.) 
  • Boiling Point: 66-67 ºC (10 mmHg),140.5 °C at 760 mmHg 
  • PKA: 13.00±0.10(Predicted) 
  • Flash Point: 154 ºF 
  • PSA: 20.23000 
  • Density: 0.893 
  • LogP: 0.78220 

2-Hexyn-1-ol(Cas 764-60-3) Usage

InChI:InChI=1/C6H10O/c1-2-3-4-5-6-7/h7H,2-3,6H2,1H3

764-60-3 Relevant articles

Synthesis of α,β-unsaturated epoxy ketones utilizing a bifunctional sulfonium/phosphonium ylide

Eskandari, Roozbeh,Hess, Jeremy P.,Tochtrop, Gregory P.

supporting information, p. 7136 - 7139 (2021/07/28)

Herein, a new protocol for rapid synthes...

Enantioselective Rhodium-Catalyzed Dimerization of ω-Allenyl Carboxylic Acids: Straightforward Synthesis of C2-Symmetric Macrodiolides

Steib, Philip,Breit, Bernhard

supporting information, p. 6572 - 6576 (2018/05/08)

Herein, we report on the first enantiose...

Gold(III)-Catalyzed Regioselective Oxidation/Cycloisomerization of Diynes: An Approach to Fused Furan Derivatives

Li, Jian,Xing, Hong-Wen,Yang, Fang,Chen, Zi-Sheng,Ji, Kegong

supporting information, p. 4622 - 4626 (2018/08/07)

The first gold(III)-catalyzed regioselec...

Sodium Phenoxide Mediated Hydroxymethylation of Alkynylsilanes with N-[(Trimethylsiloxy)methyl]phthalimide

Asano, Narumi,Sasaki, Keita,Chataigner, Isabelle,Shigeno, Masanori,Kondo, Yoshinori

supporting information, p. 6926 - 6930 (2017/12/26)

The hydroxymethylation of alkynylsilanes...

764-60-3 Process route

methyl 2-hexynoate
18937-79-6

methyl 2-hexynoate

hex-2-yn-1-ol
764-60-3

hex-2-yn-1-ol

Conditions
Conditions Yield
With diisobutylaluminium hydride; In diethyl ether; at -78 - 20 ℃; for 3h;
95%
With diisobutylaluminium hydride; In diethyl ether; at -78 ℃; for 2h;
89%
propyl bromide
106-94-5

propyl bromide

propargyl alcohol
107-19-7

propargyl alcohol

hex-2-yn-1-ol
764-60-3

hex-2-yn-1-ol

Conditions
Conditions Yield
With Iron(III) nitrate nonahydrate; ammonia; lithium; In tetrahydrofuran; at -78 - 20 ℃;
99%
With lithium amide; In tetrahydrofuran; ammonia; -30 deg C then reflux, 2 h.;
84%
With lithium amide; 1.) liq. NH3, -30 deg C, 1 h, 2.) THF, reflux, 8 h;
82.7%
propargyl alcohol; With N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium; In tetrahydrofuran; hexane; at -78 - -30 ℃; Inert atmosphere;
propyl bromide; In tetrahydrofuran; hexane; at -30 - 20 ℃; Inert atmosphere;
57%
With lithium; ferric nitrate; Yield given. Multistep reaction; 1.) liquid ammonia, dry THF, 1 h, 2.) dry THF, 2 h;
With ammonia; lithium; Yield given. Multistep reaction; 1.) 1,5 h; 2.) ether, 1 h;
With lithium amide;
propargyl alcohol; With N,N,N,N,N,N-hexamethylphosphoric triamide; n-butyllithium; In tetrahydrofuran; hexane; at -78 - -30 ℃; Inert atmosphere;
propyl bromide; In tetrahydrofuran; hexane; at -30 - 20 ℃; Inert atmosphere;

764-60-3 Upstream products

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    4-chlorobut-2-yn-1-ol

  • 925-90-6
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    ethylmagnesium bromide

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    3-(tetrahydropyran-2'-yloxy)propyne

  • 106-94-5
    106-94-5

    propyl bromide

764-60-3 Downstream products

  • 18495-25-5
    18495-25-5

    1-bromohex-2-yne

  • 928-94-9
    928-94-9

    (Z)-2-hexen-1-ol

  • 928-95-0
    928-95-0

    (E)-2-Hexen-1-ol

  • 51453-66-8
    51453-66-8

    1-chloro-3-hex-2-ynyloxy-propan-2-ol

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