ChemicalBook--->CAS DataBase List--->432047-36-4

432047-36-4

432047-36-4 Structure

432047-36-4 Structure
IdentificationBack Directory
[Name]

1-(1,3-thiazol-2-yl)ethanamine(SALTDATA: 2HCl)
[CAS]

432047-36-4
[Synonyms]

1-(2-Thiazolyl)ethylaMine
1-(Thiazol-2-yl)ethanaMine
1-(1,3-thiazol-2-yl)ethanamin
1-(thiazol-2-yl)ethan-1-amine
2-ThiazoleMethanaMine, a-Methyl-
2-ThiazoleMethanaMine, α-Methyl-
1-(thiazol-2-yl)ethanaMine hydrochloride
1-(1,3-thiazol-2-yl)ethanamine(SALTDATA: 2HCl)
[1-(1,3-Thiazol-2-yl)ethyl]amine dihydrochloride
[Molecular Formula]

C5H8N2S
[MDL Number]

MFCD18071411
[MOL File]

432047-36-4.mol
[Molecular Weight]

128.2
Chemical PropertiesBack Directory
[Boiling point ]

185℃
[density ]

1.172
[Fp ]

66℃
[storage temp. ]

2-8°C(protect from light)
[pka]

7.30±0.40(Predicted)
[Appearance]

Yellow to brown Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H332-H312-H319
[Precautionary statements ]

P261-P271-P304+P340-P312-P280-P302+P352-P312-P322-P363-P501-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

1-(1,3-thiazol-2-yl)ethanamine(SALTDATA: 2HCl)(432047-36-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

MARLTXFMRHPTOA-QPJJXVBHSA-N

944993-06-0

1-(1,3-thiazol-2-yl)ethanamine(SALTDATA: 2HCl)

432047-36-4

The general procedure for the synthesis of 1-(2-thiazolyl)ethylamine from 2-acetylthiazole oxime is as follows: Preparative Example 2: Synthesis of 1-(1,3-thiazol-2-yl)-1-ethylamine A solution was prepared by dissolving 1-(1,3-thiazol-2-yl)-1-ethanone oxime (710 mg) in methanol (10 mL). To this solution, ammonium chloride (1.35 g) and zinc powder (6.5 g) were added sequentially and the mixture was heated under reflux conditions for 2 hours. After completion of the reaction, 10% sodium hydroxide solution (10 mL) was added to the mixture and extracted three times with chloroform. The organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure and the resulting product was dried by vacuum pump to give 1-(2-thiazolyl)ethylamine (580 mg, 91% yield). Product characterization data: 1H-NMR (CDCl3): δ 1.55 (d, J = 6.8 Hz, 3H), 4.43 (q, J = 6.8 Hz, 1H), 7.24 (d, J = 3.4 Hz, 1H), 7.71 (d, J = 3.2 Hz, 1H).

[References]

[1] Patent: EP1535910, 2005, A1. Location in patent: Page/Page column 24
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