2-Hydroxy-1-(1H-indol-3-yl)ethanone

Base Information

Chemical Name:2-Hydroxy-1-(1H-indol-3-yl)ethanone
CAS No.:2400-51-3
Molecular Formula:C10H9 N O2
Molecular Weight:175.18
Hs Code.:2933990090
DSSTox Substance ID:DTXSID80178731
Nikkaji Number:J356.593I
Wikidata:Q75067236
Metabolomics Workbench ID:48279
ChEMBL ID:CHEMBL524903
Mol file:2400-51-3.mol

Synonyms:3-(hydroxyacetyl)indole

Suppliers and Price of 2-Hydroxy-1-(1H-indol-3-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

TRC
2-hydroxy-1-(1H-indol-3-yl)ethanone
50mg
$ 45.00

ChemBridge Corporation
2-hydroxy-1-(1H-indol-3-yl)ethanone 95%
5 g
$ 595.00

American Custom Chemicals Corporation
2-HYDROXY-1-(1H-INDOL-3-YL)ETHANONE 95.00%
10G
$ 3729.21

American Custom Chemicals Corporation
2-HYDROXY-1-(1H-INDOL-3-YL)ETHANONE 95.00%
5G
$ 2334.55

American Custom Chemicals Corporation
2-HYDROXY-1-(1H-INDOL-3-YL)ETHANONE 95.00%
1G
$ 1049.03

AK Scientific
2-Hydroxy-1-(1H-indol-3-yl)ethanone
1g
$ 863.00

Total 8 raw suppliers

Chemical Property of 2-Hydroxy-1-(1H-indol-3-yl)ethanone

Chemical Property:

Vapor Pressure:4.38E-07mmHg at 25°C
Melting Point:160 °C
Boiling Point:399.1°C at 760 mmHg
PKA:13.25±0.10(Predicted)
Flash Point:195.2°C
PSA：53.09000
Density:1.338g/cm³
LogP:1.34290
XLogP3:1.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:175.063328530
Heavy Atom Count:13
Complexity:205

Purity/Quality:

97% ^*data from raw suppliers

2-hydroxy-1-(1H-indol-3-yl)ethanone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=CN2)C(=O)CO

Technology Process of 2-Hydroxy-1-(1H-indol-3-yl)ethanone

There total 3 articles about 2-Hydroxy-1-(1H-indol-3-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: 97.0%

: 28755-03-5
3-chloroacetylindole

: 2400-51-3
3-(hydroxyacetyl)indole

Guidance literature:: With water; In formamide; at 110 ℃; for 3.5h;
DOI:10.1021/jo00258a009

Reference yield:

: 7269-72-9
3-indolylglyoxal

: 2400-51-3
3-(hydroxyacetyl)indole

Guidance literature:: With sodium tetrahydroborate; In tetrahydrofuran; methanol; at 0 ℃; for 0.5h; Inert atmosphere;
DOI:10.1021/acs.joc.8b02712