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274240

Sigma-Aldrich

2-Aminothiophenol

99%

Sinonimo/i:

2-Aminobenzenethiol, 2-Aminophenyl mercaptan, 2-Mercaptoaniline

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About This Item

Formula condensata:
H2NC6H4SH
Numero CAS:
137-07-5
Peso molecolare:
125.19
Beilstein:
606076
Numero CE:
205-277-3
Numero MDL:
MFCD00007702
Codice UNSPSC:
12352100
ID PubChem:
24856575
NACRES:
NA.22

Livello qualitativo

200

Saggio

99%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.642 (lit.)

P. eboll.

70-72 °C/0.2 mmHg (lit.)

Punto di fusione

16-20 °C (lit.)

Densità

1.17 g/mL at 25 °C (lit.)

Stringa SMILE

Nc1ccccc1S

InChI

1S/C6H7NS/c7-5-3-1-2-4-6(5)8/h1-4,8H,7H2
VRVRGVPWCUEOGV-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

2-Aminothiophenol is an organosulfur compound used in the synthesis of urea derivatives.

Applicazioni

2-Aminothiophenol was used in the synthesis of 1,5-benzothiazepines derivatives by reacting with 1,3-diphenylpropenone derivatives and using aluminosilicate solid catalysts. It was also used in the synthesis of benzothiazole and 3-(benzothiazol-2-yl)coumarin derivatives.

Avvertenze

Danger

Indicazioni di pericolo

H302,H314,H400

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Corr. 1B

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

174.2 °F

Punto d’infiammabilità (°C)

79 °C

Dispositivi di protezione individuale

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
MKCQ6766
MKCN0917
MKCJ7658
MKCF2937
MKCD9797

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Tianzhi Yu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 108, 274-279 (2013-03-19)
Two different types of fluorescent materials containing benzothiazolyl moiety, 2-(benzothiazol-2-yl)phenol derivatives and 3-(benzothiazol-2-yl)coumarin derivatives, were synthesized synchronously using ethyl cyanoacetate, appropriate aromatic aldehyde and 2-aminothiophenol as the starting materials under the catalysis of benzoic acid by one-pot reaction. This method
Maria J Climent et al.
ChemSusChem, 7(4), 1177-1185 (2014-03-13)
1,5-Benzothiazepines derivatives were obtained first by starting from 1,3-diphenylpropenone derivatives (chalcones) and 2-aminothiophenol by using aluminosilicate solid catalysts. However, diffusional limitations and the strong adsorption of products on the catalyst are deleterious for catalyst activity and life. Then a structured
Vikas S Patil et al.
Journal of fluorescence, 23(5), 1019-1029 (2013-05-18)
Novel ESIPT inspired benzimidazole, benzoxazole and benzothiazole were synthesized from 2,4-dihydroxy benzoic acid and 1,2-phenelenediamine, 2-aminophenol, and 2-aminothiophenol respectively. The synthesized 2-(2',4'-dihydroxyphenyl) benzimidazole, benzoxazole and benzothiazole are fluorescent and the emission characteristic are very sensitive to the micro-environment. They show
William P Morrow et al.
Archives of biochemistry and biophysics, 631, 66-74 (2017-08-23)
Thiol dioxygenases are non-heme mononuclear iron enzymes that catalyze the O
Ling-Jie Kong et al.
Analytical and bioanalytical chemistry, 404(6-7), 1653-1660 (2012-07-24)
A simple electrochemical sensor based on a molecularly imprinted polymer film as the recognition element was developed for ractopamine (RAC) detection. This is the first report of a RAC-imprinted film on a gold electrode surface, synthesized through an electrochemical method
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