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| | 1-Benzothiophen-5-amine Basic information |
| Product Name: | 1-Benzothiophen-5-amine | | Synonyms: | IFLAB-BB F0817-0001;BENZO[B]THIOPHEN-5-YLAMINE;5-AMINOBENZOTHIOPHENE;1-BENZOTHIOPHEN-5-AMINE;1-Benzothiophen-5-amine, 95+%;benzothiophen-5-amine;1-BENZOTHIEN-5-YLAMINE HYDROCHLORIDE;5-Aminobenzothiophen | | CAS: | 20532-28-9 | | MF: | C8H7NS | | MW: | 149.21 | | EINECS: | | | Product Categories: | | | Mol File: | 20532-28-9.mol |  |
| | 1-Benzothiophen-5-amine Chemical Properties |
| Melting point | 72 °C | | Boiling point | 313.1±15.0 °C(Predicted) | | density | 1.294±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | form | solid | | pka | 4.10±0.10(Predicted) | | color | Light brown to brown |
| Hazard Codes | Xn | | Risk Statements | 22 | | Safety Statements | 24/25 | | HS Code | 2934999090 |
| | 1-Benzothiophen-5-amine Usage And Synthesis |
| Definition | ChEBI: 1-Benzothiophen-5-amine is a member of 1-benzothiophenes. | | Synthesis | General procedure for the synthesis of 5-aminobenzo[b]thiophene from 5-nitrobenzo[b]thiophene: A mixture of 5-nitrobenzo[b]thiophene (3.09 g, 17.0 mmol) with 10% palladium carbon catalyst (Aldrich, Catalog No. 20,569-9) (150 mg) in ethanol (90 mL) was placed in a Parr reaction flask. The hydrogenation reaction was carried out under hydrogen atmosphere at 3 bar with continuous shaking for 16 hours. Upon completion of the reaction, the catalyst was removed by filtration through a diatomaceous earth pad and the filter cake was washed with ethanol (2 x 30 mL). The combined filtrates were concentrated under reduced pressure to afford benzo[b]thiophen-5-amine (2.57 g, 100% yield) as a dark purple amorphous solid. Its 1H NMR (CDCl3, 400 MHz) data were as follows: δ 3.70 (broad single peak, 2H), 6.78 (double peak, J = 8.61, 1.96 Hz, 1H), 7.10 (double peak, J = 2.35 Hz, 1H), 7.14 (double peak, J = 5.09 Hz, 1H), 7.38 (double peak, J = 5.48 Hz, 1H), and 7.63 (double peak, J = 8.61 Hz, 1H). | | References | [1] Patent: WO2006/66172, 2006, A1. Location in patent: Page/Page column 27
[2] Synthetic Communications, 1991, vol. 21, # 7, p. 959 - 964
[3] Journal of Medicinal Chemistry, 2002, vol. 45, # 19, p. 4128 - 4139
[4] Proceedings - Indian Academy of Sciences, Section A, 1952, # 36, p. 405,408
[5] Journal of the American Chemical Society, 1955, vol. 77, p. 5939,5943 |
| | 1-Benzothiophen-5-amine Preparation Products And Raw materials |
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