Basic information Safety Supplier Related

2,5-DIBROMOTHIAZOLE

Basic information Safety Supplier Related

2,5-DIBROMOTHIAZOLE Basic information

Product Name:
2,5-DIBROMOTHIAZOLE
Synonyms:
  • 2,5-Dibromo-1,3-thiazole
  • 2,5-DIBROMOTHIAZOLE
  • 2,5-DIBROMOTHIAZOLE 95%
  • 2,5-Dibromothiazole,97%
  • Thiazole, 2,5-dibroMo-
  • NSC 222407
  • 2,5-Dibormothiazole
  • DibromoThiazole
CAS:
4175-78-4
MF:
C3HBr2NS
MW:
242.92
EINECS:
628-983-7
Product Categories:
  • Building Blocks
  • C3 to C7
  • Chemical Synthesis
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • alkyl bromide
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • ThiazolesHeterocyclic Building Blocks
  • Heterocyclic Compounds
  • Thiazoles
  • Sulphur Derivatives
Mol File:
4175-78-4.mol
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2,5-DIBROMOTHIAZOLE Chemical Properties

Melting point:
45-49 °C (lit.)
Boiling point:
242.8±13.0 °C(Predicted)
Density 
2.324±0.06 g/cm3(Predicted)
Flash point:
110 °C
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
soluble in Methanol
pka
-0.88±0.10(Predicted)
form 
Crystalline Powder
color 
White to brown
InChI
InChI=1S/C3HBr2NS/c4-2-1-6-3(5)7-2/h1H
InChIKey
XIBIQFJKUZZLLX-UHFFFAOYSA-N
SMILES
S1C(Br)=CN=C1Br
CAS DataBase Reference
4175-78-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Harmful
HS Code 
29341000

MSDS

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2,5-DIBROMOTHIAZOLE Usage And Synthesis

Chemical Properties

White to brown crystalline powder

Uses

Used as a building block in material science.1,2

Uses

2,5-Dibromothiazole is used in the preparation of arylthiazolylpiperidine derivatives and analogs for use as survival motor neuron (SMN) protein production modulators.

Synthesis

3034-22-8

4175-78-4

2-Amino-5-bromothiazole (5.5 g, 30.72 mmol) was used as starting material and dissolved in acetonitrile (50 mL). Copper (II) bromide (3.43 g, 15.36 mmol) and isoamyl nitrite (4.9 mL, 36.87 mmol) were added sequentially. The reaction mixture was heated at 60 °C for 4 h with stirring. After completion of the reaction, the volatile solvent was removed by rotary evaporator. The residue was diluted with distilled water (50 mL) and subsequently extracted with ethyl acetate (25 mL x 2). The organic phases were combined, washed with saturated saline (50 mL) and dried over anhydrous sodium sulfate. The organic phase was concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography (60-120 mesh, eluent 10% ethyl acetate in hexane solution) to afford the target compound 2,5-dibromothiazole (5.05 g, yield 68%) as a yellow liquid. m/z 243.6 [M+2] by LCMS.

References

[1] Patent: WO2015/88045, 2015, A1. Location in patent: Paragraph 0260
[2] Patent: US2017/8885, 2017, A1. Location in patent: Paragraph 0672-0673
[3] Bulletin de la Societe Chimique de France, 1962, p. 2075 - 2078
[4] Journal of Organic Chemistry, 2017, vol. 82, # 11, p. 5947 - 5951

2,5-DIBROMOTHIAZOLESupplier

PSN Pharmaceutical Technology Co., Ltd. Gold
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