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Reputable supplier selling Thiophenethiol 7774-74-5 with stock

  • Molecular Formula: C4H4S2
  • Molecular Weight: 116.208
  • Appearance/Colour: Clear yellowish to orange liquid 
  • Vapor Pressure: 2.3mmHg at 25°C 
  • Refractive Index: n20/D 1.62(lit.)  
  • Boiling Point: 166.9 °C at 760 mmHg 
  • PKA: 6.38±0.43(Predicted) 
  • Flash Point: 54.7 °C 
  • PSA: 67.04000 
  • Density: 1.269 g/cm3 
  • LogP: 2.03680 

Thiophenethiol(Cas 7774-74-5) Usage

Preparation

By heating sodium sulfosuccinate with phosphorous trichloride; also by reduction of thiophene-2-sulfonyl chloride.

Synthesis Reference(s)

Journal of the American Chemical Society, 75, p. 6316, 1953 DOI: 10.1021/ja01120a518

InChI:InChI=1/C4H4S2/c5-4-2-1-3-6-4/h1-3,5H

7774-74-5 Relevant articles

-

Voronkov et al.

, (1974)

-

Push-pull-substituted oligo(2,5-thienyleneethynylene)s

Muehling, Bastian,Theisinger, Sonja,Meier, Herbert

, p. 1009 - 1015 (2006)

Oligo(2,5-thienyleneethynylene)s (OTE) w...

Preparation of oligo(thio-2,5-thienylenes)

Nakayama, Juzo,Katano, Naoki,Shimura, Yoshiaki,Sugihara, Yoshiaki,Ishii, Akihiko

, p. 7608 - 7610 (1996)

-

A successful chemical strategy to induce oligothiophene self-assembly into fibers with tunable shape and function

Di Maria, Francesca,Olivelli, Pasquale,Gazzano, Massimo,Zanelli, Alberto,Biasiucci, Mariano,Gigli, Giuseppe,Gentili, Denis,D'Angelo, Pasquale,Cavallini, Massimiliano,Barbarella, Giovanna

supporting information; experimental part, p. 8654 - 8661 (2011/07/29)

Functional supramolecular architectures ...

Investigation of the aroma-active compounds formed in the maillard reaction between glutathione and reducing sugars

Lee, Sang Mi,Jo, Ye-Jin,Kim, Young-Suk

experimental part, p. 3116 - 3124 (2011/08/05)

Aroma-active compounds formed during the...

PROCESS FOR PREPARING DORZOLAMIDE HYDROCHLORIDE AND ITS INTERMEDIATE

-

Page/Page column 18-19; 24-25, (2010/06/17)

The present invention relates to an impr...

A simple, fast and chemoselective method for the preparation of arylthiols

Bellale, Eknath V.,Chaudhari, Mahesh K.,Akamanchi, Krishnacharya G.

experimental part, p. 3211 - 3213 (2010/03/01)

An efficient and convenient method for t...

7774-74-5 Process route

D-Fructose
57-48-7,18875-34-8

D-Fructose

GLUTATHIONE
70-18-8

GLUTATHIONE

Thiophene-2-thiol
7774-74-5

Thiophene-2-thiol

Tetrahydrothiophen-3-one
1003-04-9

Tetrahydrothiophen-3-one

2-ethylthiophene
872-55-9

2-ethylthiophene

2-Methylpyrazine
109-08-0

2-Methylpyrazine

5-Methylfurfural
620-02-0

5-Methylfurfural

2-thiophenethanol
5402-55-1

2-thiophenethanol

1-(2-furyl)-1-ethanone
1192-62-7,80145-44-4

1-(2-furyl)-1-ethanone

2-methylthiophene-3-thiol
2527-76-6

2-methylthiophene-3-thiol

2-Acetylpyrrole
1072-83-9

2-Acetylpyrrole

2-methylfuran-3-thiol
28588-74-1

2-methylfuran-3-thiol

Conditions
Conditions Yield
In water; at 160 ℃; for 2h; pH=7.5;
D-glucose
50-99-7

D-glucose

GLUTATHIONE
70-18-8

GLUTATHIONE

1,3-thiazole
288-47-1

1,3-thiazole

Thiophene-2-thiol
7774-74-5

Thiophene-2-thiol

Tetrahydrothiophen-3-one
1003-04-9

Tetrahydrothiophen-3-one

furfural
98-01-1

furfural

2,5-DIMETHYLTHIOPHENE
638-02-8

2,5-DIMETHYLTHIOPHENE

5-Methylfurfural
620-02-0

5-Methylfurfural

1-(2-furyl)-1-ethanone
1192-62-7,80145-44-4

1-(2-furyl)-1-ethanone

2-methylthiophene-3-thiol
2527-76-6

2-methylthiophene-3-thiol

2-Acetylpyrrole
1072-83-9

2-Acetylpyrrole

2-methylfuran-3-thiol
28588-74-1

2-methylfuran-3-thiol

Conditions
Conditions Yield
In water; at 160 ℃; for 2h; pH=7.5;

7774-74-5 Upstream products

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    188290-36-0

    thiophene

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    96-43-5

    2-thienyl chloride

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    110-81-6

    Diethyl disulfide

  • 51639-98-6
    51639-98-6

    ethyldisulfanyl

7774-74-5 Downstream products

  • 3988-71-4
    3988-71-4

    2-(n-butylthio)thiophene

  • 54798-87-7
    54798-87-7

    2-(1-Thiahexyl)-thiophen

  • 6911-41-7
    6911-41-7

    2-hexylsulfanylthiophene

  • 55044-86-5
    55044-86-5

    2-nonylmercapto-thiophene

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