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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
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57-48-7,18875-34-8
D-Fructose
-
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70-18-8
GLUTATHIONE
-
-
7774-74-5
Thiophene-2-thiol
-
-
1003-04-9
Tetrahydrothiophen-3-one
-
-
872-55-9
2-ethylthiophene
-
-
109-08-0
2-Methylpyrazine
-
-
620-02-0
5-Methylfurfural
-
-
5402-55-1
2-thiophenethanol
-
-
1192-62-7,80145-44-4
1-(2-furyl)-1-ethanone
-
-
2527-76-6
2-methylthiophene-3-thiol
-
-
1072-83-9
2-Acetylpyrrole
-
-
28588-74-1
2-methylfuran-3-thiol
| Conditions | Yield |
|---|---|
|
In
water;
at 160 ℃;
for 2h;
pH=7.5;
|
-
-
50-99-7
D-glucose
-
-
70-18-8
GLUTATHIONE
-
-
288-47-1
1,3-thiazole
-
-
7774-74-5
Thiophene-2-thiol
-
-
1003-04-9
Tetrahydrothiophen-3-one
-
-
98-01-1
furfural
-
-
638-02-8
2,5-DIMETHYLTHIOPHENE
-
-
620-02-0
5-Methylfurfural
-
-
1192-62-7,80145-44-4
1-(2-furyl)-1-ethanone
-
-
2527-76-6
2-methylthiophene-3-thiol
-
-
1072-83-9
2-Acetylpyrrole
-
-
28588-74-1
2-methylfuran-3-thiol
| Conditions | Yield |
|---|---|
|
In
water;
at 160 ℃;
for 2h;
pH=7.5;
|
7774-74-5 Upstream products
-
188290-36-0
thiophene
-
96-43-5
2-thienyl chloride
-
110-81-6
Diethyl disulfide
-
51639-98-6
ethyldisulfanyl
7774-74-5 Downstream products
-
3988-71-4
2-(n-butylthio)thiophene
-
54798-87-7
2-(1-Thiahexyl)-thiophen
-
6911-41-7
2-hexylsulfanylthiophene
-
55044-86-5
2-nonylmercapto-thiophene