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

Base Information

Chemical Name:1H-indole-3,5,6-triol
CAS No.:3569-19-5
Molecular Formula:C8H7NO3
Molecular Weight:165.148
Hs Code.:
DSSTox Substance ID:DTXSID201314658
Nikkaji Number:J1.068.785C
Mol file:3569-19-5.mol

Synonyms:1H-indole-3,5,6-triol;3569-19-5;3,5,6-trihydroxyindole;SCHEMBL8150276;DTXSID201314658

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

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

Total 5 raw suppliers

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

Chemical Property:

PSA：76.48000
LogP:1.28470
XLogP3:1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:165.042593085
Heavy Atom Count:12
Complexity:176

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C2C(=CC(=C1O)O)NC=C2O

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

There total 3 articles about 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:

: 60-18-4,18875-48-4,25619-78-7,30704-25-7
L-tyrosine

: 120-72-9
indole

: 3131-52-0
1H-indole-5,6-diol

: 92-88-6
4,4'-Dihydroxybiphenyl

: 156-39-8
4-hydroxyphenylpiruvic acid

: 3569-19-5
5,6,3-trihydroxyindole

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

Guidance literature:: With ethylenediaminetetraacetic acid; oxygen; iron(II) sulfate; ascorbic acid; In water; at 30 - 32 ℃; for 2h; Product distribution; biomimetic hydroxylation, pH 6.7;

Reference yield:

: 73-22-3,27732-43-0,80206-30-0,27813-82-7
L-Tryptophan

: 120-72-9
indole

: 3131-52-0
1H-indole-5,6-diol

: 92-88-6
4,4'-Dihydroxybiphenyl

: 156-39-8
4-hydroxyphenylpiruvic acid

: 3569-19-5
5,6,3-trihydroxyindole

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

Guidance literature:: With ethylenediaminetetraacetic acid; oxygen; iron(II) sulfate; ascorbic acid; In water; at 30 - 32 ℃; for 2h; Product distribution; biomimetic hydroxylation, pH 6.7;

Reference yield:

: 138-65-8
Norepinephrine

: 3569-19-5
5,6,3-trihydroxyindole

: 490-89-1
noradrenochrome

Guidance literature:: In water-d2; at 24.9 ℃; for 0.583333h; Rate constant; Mechanism; Irradiation; other sensitizers: methylene blue, rose bengal, fluoresceine; other solvent: H₂O_.;