Basic information Safety Supplier Related

(2-Thiazolyl)methylamine

Basic information Safety Supplier Related

(2-Thiazolyl)methylamine Basic information

Product Name:
(2-Thiazolyl)methylamine
Synonyms:
  • 2-Aminomethylthiazoledihydrochloride
  • Thiazol-2-yl-methylamine
  • 2-AMINOMETHYLTHIAZOLE HYDROCHLORIDE 98%
  • C-THIAZOL-2-YL-METHYLAMINE
  • 2-AMINOMETHYLTHIAZOLE
  • 2-Aminomethyl-1,3-thiazole
  • C-Thiazol-2-Yl-Methylamine dihydrochloride
  • 2-Thiazolemethanamine
CAS:
55661-33-1
MF:
C4H6N2S
MW:
114.17
Product Categories:
  • Heterocycles
  • Amines
  • Aromatics
  • Intermediates
  • pharmacetical
Mol File:
55661-33-1.mol
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(2-Thiazolyl)methylamine Chemical Properties

Melting point:
180-185°C
Boiling point:
36 °C
Density 
1.204 g/mL at 25 °C
refractive index 
n20/D1.569
Flash point:
104℃
storage temp. 
2-8°C(protect from light)
form 
liquid
pka
7.24±0.40(Predicted)
color 
Yellow-green
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Safety Information

Hazard Codes 
Xi,C
Risk Statements 
22-34
Safety Statements 
26-36/37/39-45
RIDADR 
UN 2735PSN1 8 / PGII
HazardClass 
IRRITANT, HYGROSCOPIC, CORROSIVE
HS Code 
2934100090
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(2-Thiazolyl)methylamine Usage And Synthesis

Chemical Properties

Off-white to cream color solid

Uses

(2-Thiazolyl)methylamine is a useful compound in the preparation of cephalosporins

Synthesis

171268-82-9

7732-18-5

55661-33-1

The general procedure for the synthesis of 2-thiazole-methyl-amine from the compound (CAS: 171268-82-9) and water (electrophoretic grade) is as follows: 1. Preparation of GG1 thiazol-2-yl-methylamine azide: triphenylphosphine (2.08 g, 7.9 mmol) was added to a solution of 2-azidomethyl-thiazole (1.11 g, 7.9 mmol) in tetrahydrofuran (THF, 20 mL). 2. Reduction reaction: after 1 h, water (214 μL) and ammonium hydroxide sol (0.5 mL) were added sequentially. 3. Post-treatment: The reaction mixture was stirred overnight and subsequently concentrated under vacuum and purified by fast chromatography (eluent: 5% methanol/dichloromethane) to give the title product 2-thiazolemethanamine as a tan oil (645 mg, 72% yield). 4. The product was characterized by 1H NMR (250 MHz, CDCl3) δ 7.7 (d, 1H, J = 2.0 Hz); 7.25 (d, 1H, J = 2.0 Hz); 4.2 (s, 2H); 1.7 (bs, 2H).

References

[1] Patent: US5939398, 1999, A
[2] Patent: US5698526, 1997, A

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