1H-INDOL-3-OL
1H-INDOL-3-OL Basic information
- Product Name:
- 1H-INDOL-3-OL
- Synonyms:
-
- 3-HYDROXYINDOLE
- 1,2-Dimethylindole-3-carboxaldehyde
- 3-Hydroxy-1H-indole
- 3-Hydroxyindole,97%
- 1-Boc-1H-Indol-3-ol
- ISI-6-0026
- RARECHEM AH BS 0105
- 1,2-DIHYDRO-INDOL-3-ONE
- CAS:
- 480-93-3
- MF:
- C8H7NO
- MW:
- 133.15
- Product Categories:
-
- Indoline & Oxindole
- Mol File:
- 480-93-3.mol
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1H-INDOL-3-OL Chemical Properties
- Melting point:
- 85-87 °C
- Boiling point:
- 245.66°C (rough estimate)
- Density
- 1.1475 (rough estimate)
- refractive index
- 1.5260 (estimate)
- storage temp.
- Amber Vial, -20°C Freezer, Under inert atmosphere
- solubility
- DMSO (Slightly), Methanol (Slightly, Sonicated)
- pka
- 10.10±0.40(Predicted)
- form
- Solid
- color
- Dark Green to Black
- Stability:
- Light Sensitive
- CAS DataBase Reference
- 480-93-3(CAS DataBase Reference)
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Safety Information
- Hazard Codes
- Xi
- Hazard Note
- Irritant
- HS Code
- 2933998090
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1H-INDOL-3-OL Usage And Synthesis
Chemical Properties
1H-INDOL-3-OL is green shiny needles
Uses
1H-INDOL-3-OL is a mutation product of toluene-4-monooxygenase (T4MO), that gets spontaneously converted to indigo. Used in the preparation of indolyl-oxadiazoles with anticonvulsant activity.
Uses
3-Hydroxyindole is a mutation product of toluene-4-monooxygenase (T4MO), that gets spontaneously converted to indigo. Used in the preparation of indolyl-oxadiazoles with anticonvulsant activity.
Definition
ChEBI: A member of the class of hydroxyindoles that is 1H-indole substituted by a hydroxy group at position 3.
1H-INDOL-3-OLSupplier
J & K SCIENTIFIC LTD.
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
Capot Chemical Co., Ltd
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- +86 (0) 571 85 58 67 18
- sales@capotchem.com
Chemsky(shanghai)International Co.,Ltd.
- Tel
- 021-50135380
- shchemsky@sina.com
Santai Labs, Inc.
- Tel
- 519-85601385
- marketing@santailabs.com
Sphinx Scientific Laboratory (Tianjin) Co., Ltd.
- Tel
- 022-66211289-843 13672102692
- contact@sphinxpharm.com
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1H-INDOL-3-OL(480-93-3)Related Product Information
- 1-Acetyl-5-bromo-4-chloro-1H-indol-3-yl acetate
- 5-Bromo-4-chloro-3-indolyl-beta-D-galactoside
- 5-BROMO-4-CHLORO-3-INDOLYL ACETATE
- 3-Indoxyl-beta-D-glucopyranoside
- 3-HYDROXYINDOLE-2-CARBOXYLIC ACID METHYL ESTER
- 3-ACETOXY-5-BROMOINDOLE
- 5-BROMO-4-CHLORO-3-INDOLYL PHOSPHATE DISODIUM SALT
- 5-Bromo-4-chloro-3-indolyl phosphate p-toluidine salt
- 3-INDOXYL SULFATE POTASSIUM SALT
- 5-Bromo-4-chloro-3-indolyl-N-acetyl-beta-D-glucosaminide
- INDOXYL ACETATE
- 1,3-DIACETOXYINDOLE
- 5-BROMOINDOXYL DIACETATE
- INDOXYL BUTYRATE
- 3-INDOXYL PHOSPHATE DISODIUM SALT
- 1-(2,6-Dichlorophenyl)indolin-2-one
- Oxindole
- 1-Methyl-9H-pyrido(3,4-b)indol-7-ol, 1-Methyl-9H-pyrido[3,4-b]indol-7-ol dihydrate hydrochloride