
10075-50-0
- Product Name:5-Bromoindole
- Molecular Formula:C8H6BrN
- Purity:99%
- Molecular Weight:264.33
Product Details
pd_meltingpoint:89-92 °C
Appearance:white to light brown powder or chunks
Manufacturer supply top purity 5-Bromoindole 10075-50-0 with ISO standards
- Molecular Formula:C8H6BrN
- Molecular Weight:264.33
- Appearance/Colour:white to light brown powder or chunks
- Vapor Pressure:0.000738mmHg at 25°C
- Melting Point:89-92 °C
- Refractive Index:1.711
- Boiling Point:316.9 °C at 760 mmHg
- PKA:16.04±0.30(Predicted)
- Flash Point:145.5 °C
- PSA:15.79000
- Density:1.66 g/cm3
- LogP:2.93040
5-Bromoindole(Cas 10075-50-0) Usage
Purification Methods |
Purify it by steam distillation from a faintly alkaline solution. Cool the aqueous distillate, collect the solid, dry it in a vacuum desiccator over P2O5 and recrystallise it from aqueous EtOH (35% EtOH) or pet ether/Et2O. UV in MeOH has at 279, 287 and 296nm (log 3.70, 3.69 and 3.53). The picrate has m 137-138o(dec) (from max Et2O/pet ether). [UV: Thesing et al. Chem Ber 95 2205 1962, UV and NMR: Lallemand & Bernath Bull Soc Chim Fr 4091 1970, Beilstein 20/7 V 36.] |
InChI:InChI=1/C8H6BrN/c9-7-1-2-8-6(5-7)3-4-10-8/h1-5,10H
10075-50-0 Relevant articles
Chemoselective deprotection of allylic amines catalyzed by Grubbs' carbene
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A commercially available ruthenium compl...
Ga(DS)3-catalysed double hydroarylation of acetylenic esters with indoles for the synthesis of bisindolyl propanoates
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, p. 3996 - 3998 (2015)
Abstract An efficient synthetic method f...
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, p. 11679 - 11687 (2018)
CO2-catalyzed dehydrogenation of amines ...
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, p. 5647 - 5647 (2013)
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Novel Arylindigoids by Late-Stage Derivatization of Biocatalytically Synthesized Dibromoindigo
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, p. 5404 - 5411 (2021)
Indigoids represent natural product-base...
Hydrophobic Metal Halide Perovskites for Visible-Light Photoredox C?C Bond Cleavage and Dehydrogenation Catalysis
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DMSO/t-BuONa/O2-Mediated Aerobic Dehydrogenation of Saturated N-Heterocycles
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, p. 7501 - 7509 (2020)
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, p. 984 - 986 (2008)
The synthesis of indoles is accomplished...
Aerobic oxidative dehydrogenation of N-heterocycles over OMS-2-based nanocomposite catalysts: Preparation, characterization and kinetic study
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, p. 360 - 371 (2020)
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Dehydrogenation of indoline by cytochrome P450 enzymes: A novel "aromatase" process
Sun, Hao,Ehlhardt, William J.,Kulanthaivel, Palaniappan,Lanza, Diane L.,Reilly, Christopher A.,Yost, Garold S.
, p. 843 - 851 (2007)
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Two-Dimensional Metal-Organic Layers for Electrochemical Acceptorless Dehydrogenation of N-Heterocycles
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, p. 3557 - 3560 (2019)
The catalytic acceptorless dehydrogenati...
Synthesis of bromoindole alkaloids from Laurencia brongniartii
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A regioselective synthesis of N-carbomet...
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, p. 281 - 287 (2007)
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10075-50-0 Process route
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26807-69-2
N-acetylindololine-2-sulfonic acid sodium

-
-
10075-50-0
5-bromo-1H-indole
Conditions | Yield |
---|---|
N-acetylindololine-2-sulfonic acid sodium;
With
bromine;
In
water;
at 0 - 20 ℃;
for 2h;
With
sodium hydroxide;
In
water;
for 20h;
Reflux;
|
92% |
N-acetylindololine-2-sulfonic acid sodium;
With
bromine;
In
water;
at 0 - 20 ℃;
With
sodium hydroxide;
In
water;
for 20h;
Reflux;
|
92% |
With
bromine;
In
water;
at 0 - 5 ℃;
for 0.5h;
|
88% |
-
-
1196980-99-0
1-(5-bromo-1H-indol-1-yl)-2,2-dimethylpropan-1-one

-
-
10075-50-0
5-bromo-1H-indole
Conditions | Yield |
---|---|
With
water; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
tetrahydrofuran;
at 20 ℃;
for 24h;
|
99% |
10075-50-0 Upstream products
-
5-bromoindoline
-
5-bromo-2-indolecarboxylic acid
-
N-(4-bromophenyl)ethenesulfinamide
-
5-Bromo-1-(methylsulfonyl)indole
10075-50-0 Downstream products
-
5-bromo-1H-indole-3-carboxaldehyde
-
5-Bromo-indole-3-carbinol
-
2-(5-bromo-1H-indol-3-yl)-2-oxoacetyl chloride
-
5-methylthio-1H-indole
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