ChemicalBook--->CAS DataBase List--->34843-84-0

34843-84-0

34843-84-0 Structure

34843-84-0 Structure
IdentificationBack Directory
[Name]

3-AMINOETHYLTHIOPHENE HCL
[CAS]

34843-84-0
[Synonyms]

2-(Thiophen-3-yl)
3-AMino-ethyl thiophene
3-AMINOETHYLTHIOPHENE HCL
3-aminoethylthiophene hydrochloride
3-Thiopheneethanamine hydrochloride
Thiophene-3-ethylaMine hydrochloride
2-(3-Thienyl)ethanamine hydrochloride
2-(3-thienyl)ethylaMine hydrochloride
2-(Thien-3-yl)ethylamine hydrochloride
3-(2-Aminoethyl)thiophene hydrochloride
2-Thiophen-3-yl-ethylamine hydrochloride
2-(thiophen-3-yl)ethan-1-aMine hydrochloride
3-AMINOETHYLTHIOPHENE HCL ISO 9001:2015 REACH
[Molecular Formula]

C6H10ClNS
[MDL Number]

MFCD00176329
[MOL File]

34843-84-0.mol
[Molecular Weight]

163.67
Chemical PropertiesBack Directory
[Melting point ]

215-216℃
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[Appearance]

White to off-white Powder
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319
[Precautionary statements ]

P501-P261-P270-P271-P264-P280-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P302+P352+P312-P304+P340+P312
[HazardClass ]

IRRITANT
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINOETHYLTHIOPHENE HCL(34843-84-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Cyanomethylthiophene

13781-53-8

3-AMINOETHYLTHIOPHENE HCL

34843-84-0

The general procedure for the synthesis of 3-thiophene ethylamine hydrochloride from 3-thiopheneacetonitrile was as follows: thiophen-3-ylacetonitrile (2.0 g, 16.2 mmol) was dissolved in tetrahydrofuran (36 mL), and borane-dimethyl sulfide complex (3.0 mL, 30.4 mmol) was slowly added. The reaction mixture was heated to reflux for 16 hours. Upon completion of the reaction, methanol was added slowly at room temperature to terminate the reaction. Subsequently, saturated HCl/methanol solution (10 mL) was added and stirred at room temperature for 20 minutes. The reaction solution was concentrated to give the initial solid product. The solid was washed with ether (20 mL) to afford the target compound 3-thiophene ethylamine hydrochloride (Compound 41A) as a white solid (2.5 g, yield: 94%).

[References]

[1] Patent: CN108250128, 2018, A. Location in patent: Paragraph 0698; 0700; 0701; 0702
[2] Patent: WO2007/146759, 2007, A2. Location in patent: Page/Page column 24
[3] Patent: WO2007/146758, 2007, A2. Location in patent: Page/Page column 33
[4] Journal of Medicinal Chemistry, 2014, vol. 57, # 9, p. 3687 - 3706
[5] Patent: WO2012/114252, 2012, A1. Location in patent: Page/Page column 46
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