Basic information Safety Supplier Related

5-BROMO-2-METHYLINDOLE

Basic information Safety Supplier Related

5-BROMO-2-METHYLINDOLE Basic information

Product Name:
5-BROMO-2-METHYLINDOLE
Synonyms:
  • 2-METHYL-5-BROMO INDOLE
  • 5-BROMO-2-METHYLINDOLE
  • 5-BROMO-2-METHYL-1H-INDOLE
  • 1H-Indole, 5-bromo-2-methyl-
CAS:
1075-34-9
MF:
C9H8BrN
MW:
210.07
Product Categories:
  • Indole
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Indoles
  • IndolesBuilding Blocks
Mol File:
1075-34-9.mol
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5-BROMO-2-METHYLINDOLE Chemical Properties

Melting point:
104-107 °C (lit.)
Boiling point:
147-148 °C(Press: 4 Torr)
Density 
1.4916 g/cm3
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
16.61±0.30(Predicted)
form 
Powder
color 
Yellow to pink to tan
CAS DataBase Reference
1075-34-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2933998090

MSDS

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5-BROMO-2-METHYLINDOLE Usage And Synthesis

General Description

5-Bromo-2-methylindole, a bromoalkylindole derivative, has been reported to be prepared by the bromination of 2-methylindole and characterized by 1H NMR.

Synthesis

95-20-5

1075-34-9

Step 1. Synthesis of 5-bromo-2-methyl-7H-indole: To a solution of 2-methyl-1H-indole (5.0 g, 38.12 mmol) in sulfuric acid (80 mL) was added Ag2SO4 (12.5 g, 40.06 mmol) under cooling in an ice bath and stirred for 30 min. Subsequently, Br2 (6.4 g, 40.05 mmol) was slowly added dropwise over 30 minutes. After the dropwise addition, the reaction mixture was continued to be stirred at room temperature for 4 hours. Upon completion of the reaction, the reaction was quenched by the addition of a water/ice mixture (300 mL). The reaction mixture was extracted with dichloromethane (3 x 200 mL), the organic layers were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford 5-bromo-2-methyl-7H-indole as a light brown solid (6 g). The product was detected by LC-MS: [M+H]+ m/z 211.0. 1H-NMR (300MHz, CDCl3) δ: 11.23 (s, 1H), 7.56 (s, 1H), 7.21 (d, J=8.7Hz, 1H), 7.07-7.09 (m, 1H), 6.11 (s, 1H), 2.38 (s, 3H).

References

[1] Patent: WO2012/119046, 2012, A2. Location in patent: Page/Page column 161
[2] Patent: US2012/225863, 2012, A1. Location in patent: Page/Page column 28

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