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2-bromo-3-methyl-1H-indole

Base Information
  • Chemical Name:2-bromo-3-methyl-1H-indole
  • CAS No.:1484-28-2
  • Molecular Formula:C9H8BrN
  • Molecular Weight:210.073
  • Hs Code.:
  • European Community (EC) Number:630-837-2
  • Nikkaji Number:J910.147K
  • Mol file:1484-28-2.mol
2-bromo-3-methyl-1H-indole

Synonyms:2-bromo-3-methyl-1H-indole;1484-28-2;2-bromo-3-methylindole;2-brom-3-methyl-1H-indole;SCHEMBL8089252

Suppliers and Price of 2-bromo-3-methyl-1H-indole
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Crysdot
  • 2-Bromo-3-methyl-1H-indole 95+%
  • 1g
  • $ 1081.00
  • Chemenu
  • 2-bromo-3-methyl-1H-indole 95%
  • 1g
  • $ 1018.00
  • Alichem
  • 2-Bromo-3-methyl-1H-indole
  • 1g
  • $ 953.75
Total 6 raw suppliers
Chemical Property of 2-bromo-3-methyl-1H-indole
Chemical Property:
  • Melting Point:85-86 °C 
  • Boiling Point:324.7±22.0 °C(Predicted) 
  • PKA:15?+-.0.30(Predicted) 
  • Density:1.563±0.06 g/cm3(Predicted) 
  • Storage Temp.:2-8°C 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:208.98401
  • Heavy Atom Count:11
  • Complexity:149
Purity/Quality:

99% *data from raw suppliers

2-Bromo-3-methyl-1H-indole 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1=C(NC2=CC=CC=C12)Br
Technology Process of 2-bromo-3-methyl-1H-indole

There total 3 articles about 2-bromo-3-methyl-1H-indole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With N-Bromosuccinimide; In tetrachloromethane; for 3h;
DOI:10.1016/j.tetlet.2003.12.020
Guidance literature:
With t-butyl bromide; In dimethyl sulfoxide; at 40 ℃; for 1.9h;
upstream raw materials:

3-Methylindole

Downstream raw materials:

1-benzyl-2-bromo-3-methyl-1H-indole

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