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4-Bromo-3,5-dimethylisoxazole

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4-Bromo-3,5-dimethylisoxazole Basic information

Product Name:
4-Bromo-3,5-dimethylisoxazole
Synonyms:
  • BUTTPARK 33\06-98
  • 4-BROMO-3,5-DIMETHYLISOXAZOLE
  • 4-BROMO-3,5-DIMETHYLISOXAZOLE 97%
  • Isoxazole, 4-broMo-3,5-diMethyl-
  • 4-Bromo-3,5-dimethylisoxazole, tech.
  • 4-Bromo-3,5-dimethylisoxazole,97%
  • 4-Bromo-3,5-dimethylisoxa...
  • TIMTEC-BB SBB003784
CAS:
10558-25-5
MF:
C5H6BrNO
MW:
176.01
EINECS:
000-000-0
Product Categories:
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Isoxazoles
  • IsoxazolesBuilding Blocks
  • Oxazole&Isoxazole
  • blocks
  • Bromides
  • Oxazoles
Mol File:
10558-25-5.mol
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4-Bromo-3,5-dimethylisoxazole Chemical Properties

Boiling point:
176 °C(lit.)
Density 
1.478 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.486(lit.)
Flash point:
>230 °F
storage temp. 
2-8°C
pka
-2.35±0.28(Predicted)
form 
clear liquid
color 
Colorless to Light orange to Yellow
Sensitive 
Light Sensitive
BRN 
108522
InChI
InChI=1S/C5H6BrNO/c1-3-5(6)4(2)8-7-3/h1-2H3
InChIKey
GYHZPSUAMYIFQD-UHFFFAOYSA-N
SMILES
O1C(C)=C(Br)C(C)=N1
CAS DataBase Reference
10558-25-5(CAS DataBase Reference)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
Hazard Note 
Keep Cold/Light Sensitive
HS Code 
29349990

MSDS

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4-Bromo-3,5-dimethylisoxazole Usage And Synthesis

Chemical Properties

clear colorless to light yellow liquid

Uses

4-Bromo-3,5-dimethylisoxazole may be used in the preparation of (tert-butyldimethylsilyl)-(3,5-dimethylisoxazol-4-yl)phenylamine and 3,3′,5,5′-tetramethyl-4,4′-diisoxazole.[21}

General Description

4-Bromo-3,5-dimethylisoxazole is also known as 3,5-dimethyl-4-bromoisoxazole.

Synthesis

300-87-8

10558-25-5

The general procedure for the synthesis of 4-bromo-3,5-dimethylisoxazole from 3,5-dimethylisoxazole is as follows: 1. Preparation of intermediate 105 (4-bromo-3,5-dimethyl-1,2-oxazole): DMF (53 mL) was added to a 250 mL round-bottomed flask fitted with a magnetic stirrer. 2. 3,5-dimethyl-1,2-oxazole (5.3 g, 54.57 mmol) and N-iodosuccinimide (11.659 g, 65.49 mmol) were sequentially added to the stirred DMF. 3. After completion of the addition, the reaction mixture was heated to 75°C and maintained for 3 hours. 4. Upon completion of the reaction, the mixture was diluted with ethyl acetate (100 mL). 5. The organic layer was washed sequentially with saturated NaHCO3 solution (100 mL), sodium thiosulfate solution (100 mL), water (200 mL) and brine (100 mL). 6. The organic layer was dried over anhydrous Na2SO4 and then concentrated under reduced pressure to remove the solvent to afford the target product 4-bromo-3,5-dimethyl-1,2-oxazole (6.1 g, 63.4% yield).

References

[1] Patent: WO2012/11125, 2012, A1. Location in patent: Page/Page column 148; 149
[2] Rend. Ist. lomb., 1936, vol. 69, p. 587,600

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