• Product Name2-Butene-1,4-diol
  • CasNo. 6117-80-2
  • MFC4H8O2
  • MW88.1063
  • Purity
  • Appearanceclear liquid
  • Packing
  • Contact usInquiry

Product Details

CasNo: 6117-80-2

MF: C4H8O2

Appearance: clear liquid

Trustworthy Manufacturer Supply Top Purity 99% 6117-80-2 with Competitive Price

  • Molecular Formula:C4H8O2
  • Molecular Weight:88.1063
  • Appearance/Colour:clear liquid 
  • Vapor Pressure:0.87Pa at 25℃ 
  • Melting Point:4-10 °C 
  • Refractive Index:n20/D 1.479  
  • Boiling Point:234.999 °C at 760 mmHg 
  • PKA:13.88±0.10(Predicted) 
  • Flash Point:85.384 °C 
  • PSA:40.46000 
  • Density:1.059 g/cm3 
  • LogP:-0.47280 

2-Butene-1,4-diol(Cas 6117-80-2) Usage

InChI:InChI=1/C4H8O2/c5-3-1-2-4-6/h1-2,5-6H,3-4H2/b2-1-

6117-80-2 Relevant articles

One-step synthesis of Pt@ZIF-8 catalyst for the selective hydrogenation of 1,4-butynediol to 1,4-butenediol

Li, Chuang,Zhang, Mingming,Di, Xin,Yin, Dongdong,Li, Wenzhen,Liang, Changhai

, p. 1555 - 1561 (2016)

A catalyst consisting of platinum nanopa...

PVP-Pd@ZIF-8 as highly efficient and stable catalysts for selective hydrogenation of 1,4-butynediol

Zhang, Mingming,Yang, Yuebin,Li, Chuang,Liu, Qian,Williams, Christopher T.,Liang, Changhai

, p. 329 - 332 (2014)

Cubic Pd nanoparticles were rapidly enca...

An excellent nickel boride catalyst for the cis-selective semihydrogenation of acetylenes

Choi, Jaesung,Yoon, Nung Min

, p. 1057 - 1060 (1996)

Internal alkynes were hydrogenated quant...

Parahydrogen-Induced Polarization Relayed via Proton Exchange

Them, Kolja,Ellermann, Frowin,Pravdivtsev, Andrey N.,Salnikov, Oleg G.,Skovpin, Ivan V.,Koptyug, Igor V.,Herges, Rainer,H?vener, Jan-Bernd

supporting information, p. 13694 - 13700 (2021/09/07)

The hyperpolarization of nuclear spins i...

Highly selective semi-hydrogenation of alkynes with a Pd nanocatalyst modified with sulfide-based solid-phase ligands

Huang, Lingqi,Hu, Kecheng,Ye, Ganggang,Ye, Zhibin

, (2021/03/30)

Soluble small molecular/polymeric ligand...

Dehydrogenative alcohol coupling and one-pot cross metathesis/dehydrogenative coupling reactions of alcohols using Hoveyda-Grubbs catalysts

?zer, Halenur,Arslan, Dilan,?ztürk, Bengi ?zgün

, p. 5992 - 6000 (2021/04/12)

In this study,in situformed ruthenium hy...

Continuous Flow Z-Stereoselective Olefin Metathesis: Development and Applications in the Synthesis of Pheromones and Macrocyclic Odorant Molecules**

Browne, Duncan L.,Colombel-Rouen, Sophie,Crévisy, Christophe,Curbet, Idriss,Mauduit, Marc,McBride, Tom,Morvan, Jennifer,Roisnel, Thierry

supporting information, p. 19685 - 19690 (2021/08/06)

The first continuous flow Z-selective ol...

6117-80-2 Process route

1,4-dihydroxybut-2-yne
110-65-6

1,4-dihydroxybut-2-yne

1,4-butenediol
6117-80-2

1,4-butenediol

Conditions
Conditions Yield
With quinoline; hydrogen; Lindlar's catalyst; In methanol; at 0 ℃;
100%
With borane-ammonia complex; Cu2O; In ethanol; at 50 ℃; for 0.75h; stereoselective reaction; Sealed tube; Green chemistry;
100%
With hydrogen; copper-palladium; silica gel; In ethanol; at 25 ℃; under 760.051 Torr;
99%
With piperazine; hydrogen; In ethanol; at 80 ℃; for 24h; under 4500.45 Torr; diastereoselective reaction;
99%
With hydrogen; montmorillonit-bipyridinpalladium(II)-acetate; In tetrahydrofuran; Ambient temperature;
98%
With quinoline; hydrogen; Lindlar's catalyst; In various solvent(s); at 20 ℃; for 2h; under 760.051 Torr;
98%
With hydrogen; In methanol; at 20 ℃; for 5.5h; under 760.051 Torr; Green chemistry;
98%
With hydrogen; In methanol; for 5.5h; under 760.051 Torr; Time;
97%
With borohydride exchange resin; hydrogen; nickel diacetate; In methanol; at 0 ℃; for 1h; under 760 Torr;
94%
With hydrogen; In ethanol; at 100 ℃; for 24h; under 7500.75 Torr; chemoselective reaction;
94%
With hydrogen; palladium amalgam; silica gel; In ethyl acetate; for 16h; under 760 Torr; Ambient temperature;
92%
With pyridine; hydrogen; In ethyl acetate; at 25 ℃;
90%
With hydrogen; quinoline; In ethanol; at 25 ℃; under 760 Torr;
80%
With copper; zinc; In methanol; for 2h; Heating;
57%
With methanol; nickel; at 25 - 50 ℃; Hydrogenation;
 
With methanol; palladium on activated charcoal; Hydrogenation;
 
With water; iron; at 50 ℃; Hydrogenation.unter Druck;
 
With copper; Hydrogenation;
 
With nickel; Hydrogenation;
 
With cobalt; Hydrogenation;
 
With platinum; Hydrogenation;
 
With zinc copper; ethanol;
 
With potassium hydroxide; Reduktion an einer versilberten Kupfer-Kathode;
 
With ethanol; nickel; at 25 - 50 ℃; Hydrogenation;
 
With hydrogen; ruthenium palladium;
 
With hydrogen; In water; at 50 ℃; under 15001.5 Torr; Reagent/catalyst; Temperature; Pressure; chemoselective reaction; Catalytic behavior; Kinetics;
 
With hydrogen; In ethanol; at 20 ℃; under 750.075 Torr; chemoselective reaction;
 
With hydrogen; In water; at 120 ℃; for 6h; under 15001.5 Torr; Pressure; Temperature; Time;
 
With hydrogen; In methanol; at 20 ℃; for 8h; Reagent/catalyst; Flow reactor;
 
With [1,4-bis(diphenylphosphino)butane](1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; para-hydrogen; In [(2)H6]acetone; for 0.0166667h; under 760.051 Torr; Solvent; Mechanism;
 
1,4-dihydroxybut-2-yne
110-65-6

1,4-dihydroxybut-2-yne

2-hydroxytetrahydrofuran
5371-52-8

2-hydroxytetrahydrofuran

Butane-1,4-diol
110-63-4

Butane-1,4-diol

1,4-butenediol
6117-80-2

1,4-butenediol

Conditions
Conditions Yield
With hydrogen; Montmorillonite-Ph2PPd(II); In tetrahydrofuran; at 25 ℃; for 2h; under 760 Torr; Product distribution; other catalysts (5percent Pd-C, Lindlar catalyst), other solvents (ethyl acetate);
 

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