1-(5-bromo-1H-indol-2-yl)Ethanone

Base Information

Chemical Name:1-(5-bromo-1H-indol-2-yl)Ethanone
CAS No.:89671-83-0
Molecular Formula:C10H8BrNO
Molecular Weight:238.084
Hs Code.:
DSSTox Substance ID:DTXSID70525679
Nikkaji Number:J1.930.643G
Wikidata:Q82393451
Mol file:89671-83-0.mol

Synonyms:1-(5-bromo-1H-indol-2-yl)Ethanone;89671-83-0;1-(5-Bromo-1H-indol-2-yl)ethan-1-one;2-acetyl-5-bromoindole;SCHEMBL2729921;DTXSID70525679;AKOS014668645;CS-0240173;EN300-226234;G54012

Suppliers and Price of 1-(5-bromo-1H-indol-2-yl)Ethanone

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

Chemenu
1-(5-Bromo-1H-indol-2-yl)ethanone 95%+
1g
$ 624.00

Chemenu
1-(5-Bromo-1H-indol-2-yl)ethanone 95%+
5g
$ 1870.00

Alichem
1-(5-Bromo-1H-indol-2-yl)ethanone
25g
$ 6472.20

Alichem
1-(5-Bromo-1H-indol-2-yl)ethanone
10g
$ 3693.04

Alichem
1-(5-Bromo-1H-indol-2-yl)ethanone
5g
$ 2436.12

AK Scientific
1-(5-Bromo-1H-indol-2-yl)Ethanone
1g
$ 676.00

AK Scientific
1-(5-Bromo-1H-indol-2-yl)Ethanone
500mg
$ 532.00

AK Scientific
1-(5-Bromo-1H-indol-2-yl)Ethanone
100mg
$ 262.00

Total 5 raw suppliers

Chemical Property of 1-(5-bromo-1H-indol-2-yl)Ethanone

Chemical Property:

PSA：32.86000
LogP:3.13300
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:236.97893
Heavy Atom Count:13
Complexity:219

Purity/Quality:

98% ^*data from raw suppliers

1-(5-Bromo-1H-indol-2-yl)ethanone 95%+ ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=CC2=C(N1)C=CC(=C2)Br

Technology Process of 1-(5-bromo-1H-indol-2-yl)Ethanone

There total 6 articles about 1-(5-bromo-1H-indol-2-yl)Ethanone 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:

Reference yield: 92.0%

: 79570-74-4
2-Acetyl-5-bromo-1H-indole-3-carboxylic acid

: 89671-83-0
1-(5-bromo-1H-indol-2-yl)ethan-1-one

Guidance literature:: With sodium hydroxide; In pyridine; Heating;
DOI:10.1007/BF00515352

Reference yield: 68.0%

: 1016481-05-2
5-bromo-1H-indole-2-carboxylic acid N-methoxy-N-methyl amide

: 917-54-4
methyllithium

: 89671-83-0
1-(5-bromo-1H-indol-2-yl)ethan-1-one

Guidance literature:: In tetrahydrofuran; diethyl ether; at -78 ℃; for 3h;

Reference yield: 65.0%

: C₁₀H₈BrNO₃

: 89671-83-0
1-(5-bromo-1H-indol-2-yl)ethan-1-one

Guidance literature:: With bis(N,N-dimethylformamide)dichlorodioxomolybdenum(VI); triphenylphosphine; In toluene; at 200 ℃; for 0.5h; Inert atmosphere; Microwave irradiation;