1H-Indol-2-ol

Base Information

Chemical Name:1H-Indol-2-ol
CAS No.:16990-73-1
Molecular Formula:C8H7 N O
Molecular Weight:133.15
Hs Code.:2933990090
European Community (EC) Number:241-069-9
DSSTox Substance ID:DTXSID10937712
Nikkaji Number:J318.319J
Wikidata:Q82913926
Mol file:16990-73-1.mol

Synonyms:1,3-dihydro-2h-indol-2-one;1,3-dihydroindol-2-one;1h-indol-2-ol;2-hydroxyindole;2-indolinone;2-oxindole;2-oxindole perchlorate;2h-indol-2-one, 1,3-dihydro-;diclofenac impurity E;indol-2(3h)-one;indol-2-ol;indoline-2-one;oxindole

Suppliers and Price of 1H-Indol-2-ol

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-Hydroxyindole
250mg
$ 45.00

Crysdot
1H-Indol-2-ol 97%
1g
$ 455.00

American Custom Chemicals Corporation
2-HYDROXYINDOLE 95.00%
5G
$ 1553.48

Alichem
1H-Indol-2-ol
100g
$ 159.00

AK Scientific
2,3-Dihydroindol-2-one
25g
$ 41.00

aablocks
2-Hydroxyindole 97%
500g
$ 323.00

aablocks
2-Hydroxyindole 97%
100g
$ 95.00

aablocks
2-Hydroxyindole 97%
25g
$ 30.00

aablocks
2-Hydroxyindole 97%
5g
$ 15.00

Total 26 raw suppliers

Chemical Property of 1H-Indol-2-ol

Chemical Property:

Vapor Pressure:3.61E-05mmHg at 25°C
Boiling Point:343.2°Cat760mmHg
Flash Point:161.4°C
PSA：36.02000
Density:1.327g/cm³
LogP:1.87350
Storage Temp.:Keep in dark place,Inert atmosphere,Room temperature
XLogP3:2.4
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:

97% ^*data from raw suppliers

2-Hydroxyindole ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=C(N2)O

Technology Process of 1H-Indol-2-ol

There total 2 articles about 1H-Indol-2-ol 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:

: 120-72-9
indole

: 16990-73-1
2-Hydroxyindole

: 480-93-3
indoxyl

: 479-41-4
indirubin

: 482-89-3,12626-73-2
1H,1H'-2,2'-Biindolylidene-3,3'-dione

Guidance literature:: With P₄₅₀ BM-3 mutant; NADPH; In water; dimethyl sulfoxide; for 0.333333h; pH=8.2; Further Variations:; Reagents; Kinetics;
DOI:10.1002/(SICI)1521-3765(20000502)6:9<1531::AID-CHEM1531>3.3.CO;2-4