Basic information Safety Supplier Related

2-Amino-4-phenylthiazole

Basic information Safety Supplier Related

2-Amino-4-phenylthiazole Basic information

Product Name:
2-Amino-4-phenylthiazole
Synonyms:
  • 4-phenyl-1,3-thiazol-2-ylamine
  • 2-Thiazolamine, 4-phenyl-
  • 2-Amino-4-phenyl-1,3-thiazole
  • 2-Thiazolamine, 4-phenyl- (9CI)
  • 4-phenylthiazol-2-amine hydrobromide
  • 4-phenyl-2-amino-1,3-thiazole
  • WLN: T5N CSJ BZ ER
  • IFLAB-BB F1386-0378
CAS:
2010-06-2
MF:
C9H8N2S
MW:
176.24
EINECS:
217-926-8
Product Categories:
  • Building Blocks
  • C8 to C9
  • Building Blocks
  • Heterocyclic Building Blocks
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Amines
  • Thiazoles, Isothiazoles & Benzothiazoles
  • Thiazoles
Mol File:
2010-06-2.mol
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2-Amino-4-phenylthiazole Chemical Properties

Melting point:
149-153 °C (lit.)
Boiling point:
363.4±11.0 °C(Predicted)
Density 
1.261±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
DMF: 10 mg/ml; DMSO: 10 mg/ml; Ethanol: 12 mg/ml; Ethanol:PBS (pH 7.2) (1:10): 0.1 mg/ml
pka
4.33±0.10(Predicted)
form 
Crystalline Solid
color 
White to yellow to pale orange
λmax
284nm(EtOH)(lit.)
BRN 
128609
InChIKey
PYSJLPAOBIGQPK-UHFFFAOYSA-N
CAS DataBase Reference
2010-06-2(CAS DataBase Reference)
NIST Chemistry Reference
2-Thiazolamine, 4-phenyl-(2010-06-2)
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Safety Information

Hazard Codes 
Xn,Xi,T
Risk Statements 
22-37/38-41-25
Safety Statements 
26-36/37/39-45
RIDADR 
UN 2811 6.1 / PGIII
WGK Germany 
3
RTECS 
XJ2878000
HazardClass 
IRRITANT
HazardClass 
6.1
PackingGroup 
III
HS Code 
29341000
Toxicity
mouse,LD50,intravenous,320mg/kg (320mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#00815,

MSDS

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2-Amino-4-phenylthiazole Usage And Synthesis

Description

2-amino-4-phenyl Thiazole is a synthetic intermediate useful for pharmaceutical synthesis.

Uses

4-Phenyl-2-thiazolamine was used to prepare suberoylanilide hydroxamic acid (SAHA) analogs with cancer cell growth inhibitory activities. It was also used to synthesize ketone histone deacetylase inhibitors with antitumor activity in vivo.

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