1-Methyl-1H-indole-3,5,6-triol

Base Information Edit

Chemical Name:1-Methyl-1H-indole-3,5,6-triol
CAS No.:642-75-1
Molecular Formula:C9H9 N O3
Molecular Weight:179.175
Hs Code.:2933990090
UNII:0E3D10P8H9
Nikkaji Number:J12.291B
Wikidata:Q63392630
Mol file:642-75-1.mol

Synonyms:3,5,6-trihydroxy-1-methylindole;adrenolutin

Suppliers and Price of 1-Methyl-1H-indole-3,5,6-triol

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
1-Methyl-1H-indole-3,5,6-triol
10mg
$ 215.00

Medical Isotopes, Inc.
1-Methyl-1H-indole-3,5,6-triol
100 mg
$ 2400.00

Medical Isotopes, Inc.
1-Methyl-1H-indole-3,5,6-triol
10 mg
$ 675.00

American Custom Chemicals Corporation
ADRENOLUTIN 95.00%
5MG
$ 504.00

Total 4 raw suppliers

Chemical Property of 1-Methyl-1H-indole-3,5,6-triol Edit

Chemical Property:

Vapor Pressure:4.49E-09mmHg at 25°C
Melting Point:236° (dec); mp 195° (Balsinger); mp 245°
Boiling Point:459.8°C at 760 mmHg
Flash Point:231.9°C
PSA：60.77000
Density:1.457g/cm³
LogP:0.79530
Storage Temp.:-20°C Freezer
Solubility.:Methanol (Slightly)
XLogP3:0.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:179.058243149
Heavy Atom Count:13
Complexity:199

Purity/Quality:

99%, ^*data from raw suppliers

1-Methyl-1H-indole-3,5,6-triol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C=C(C2=CC(=C(C=C21)O)O)O
Uses 1-Methyl-1H-indole-3,5,6-triol is used in biological studies as amlodipine effect on neurohormones and oxidative stress in nonischemic cardiomyopathy.

Technology Process of 1-Methyl-1H-indole-3,5,6-triol

There total 2 articles about 1-Methyl-1H-indole-3,5,6-triol 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:

: 329-65-7,51028-73-0
Epinephrine

: 642-75-1
adrenolutine

: 54-06-8
adrenochrome

Guidance literature:: In water-d2; at 24.9 ℃; for 5.83333h; Rate constant; Mechanism; Irradiation; other sensitizers: methylene blue, rose bengal, fluoresceine, superoxide dismutase; other inhibitors: 1,3-diphenylisobenzofuran, 1,4-diazobicyclo<2,2,2>octane, KN3, NaN3; other solvent: H2O.;