6-Hydroxyindole

Base Information Edit

Chemical Name:6-Hydroxyindole
CAS No.:2380-86-1
Molecular Formula:C8H7NO
Molecular Weight:133.15
Hs Code.:29339900
European Community (EC) Number:417-020-4,626-440-9
UNII:3I03JZ599T
DSSTox Substance ID:DTXSID20178497
Nikkaji Number:J467.722F
Wikidata:Q27257236
Metabolomics Workbench ID:129004
ChEMBL ID:CHEMBL2413822
Mol file:2380-86-1.mol

Synonyms:6-hydroxyindole

Suppliers and Price of 6-Hydroxyindole

Supply Marketing:Edit

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
6-Hydroxyindole
500mg
$ 50.00

SynQuest Laboratories
6-Hydroxy-1H-indole
5 g
$ 264.00

SynQuest Laboratories
6-Hydroxy-1H-indole
250 mg
$ 40.00

SynQuest Laboratories
6-Hydroxy-1H-indole
1 g
$ 112.00

Sigma-Aldrich
6-Hydroxyindole ≥99.0% (GC)
1 g
$ 182.00

Sigma-Aldrich
6-Hydroxyindole ≥99.0% (GC)
1g-f
$ 199.00

Matrix Scientific
6-Hydroxyindole 98%
5g
$ 188.00

Matrix Scientific
6-Hydroxyindole 98%
1g
$ 41.00

Frontier Specialty Chemicals
6-Hydroxyindole 98%
250mg
$ 49.00

Frontier Specialty Chemicals
6-Hydroxyindole 98%
1g
$ 141.00

Total 154 raw suppliers

Chemical Property of 6-Hydroxyindole Edit

Chemical Property:

Appearance/Colour:White to off-white shiny crystalline powder
Vapor Pressure:0.000369mmHg at 25°C
Melting Point:124-130 °C
Refractive Index:1.694
Boiling Point:343.2 °C at 760 mmHg
PKA:10.07±0.40(Predicted)
Flash Point:161.4 °C
PSA：36.02000
Density:1.327 g/cm³
LogP:1.87350
Storage Temp.:Keep Cold
XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:133.052763847
Heavy Atom Count:10
Complexity:126

Purity/Quality:

99% ^*data from raw suppliers

6-Hydroxyindole ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi, N, Xn
Hazard Codes:Xi,N,Xn
Statements: 36/37/38-51/53-43-41-22
Safety Statements: 37/39-26-61-24-2

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1=CC(=CC2=C1C=CN2)O
Uses Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulatorsReactant for asymmetrical synthesis of notoamide J as a potential biosynthetic precursor of prenylated indole alkaloidsReactant for preparation of (quinolinyloxymethyl)isoxazolecarboxylate esters antituberculosis agentsReactant for preparation of indolyl(propanolamine) derivatives as HIV inhibitorsReactant for preparation of indoleoxyacetic acid derivatives as peroxisome proliferator-activated receptor agonistsReactant for preparation of 1-aroylindole 3-aroylindoles combretastatin A-4 analogs as antitumor agents and tubulin polymerization inhibitors

Technology Process of 6-Hydroxyindole

There total 5 articles about 6-Hydroxyindole 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: 96.0%