ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Indole Compounds >1H-Indol-2-ylmethanol

1H-Indol-2-ylmethanol

1H-Indol-2-ylmethanol Suppliers list
Company Name: Baiyin Chengze Chemical Technology Co., Ltd.  Gold
Tel: +86 943-8535351 13389336721
Email: sales@chengzechem.com
Company Name: Shandong Liteng Biotechnology Co., Ltd  Gold
Tel: 15020019777 18663721413
Email: rosy@litengpharm.com
Company Name: Shaanxi Hydrotransformer Energy Technology Co., Ltd.  Gold
Tel: 18700580159 18700580159
Email: info@hydrotransformer.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Accela ChemBio Co.,Ltd.  
Tel: 021-50795510 4000665055
Email: marketing@accelachem.com

1H-Indol-2-ylmethanol manufacturers

1H-Indol-2-ylmethanol Basic information
Product Name:1H-Indol-2-ylmethanol
Synonyms:2-HYDROXYMETHYLINDOLE;1H-Indole-2-methanol;NSC 165230;indol-2-ylmethan-1-ol;2-(Hydroxymethyl)-1H-indole 97+%;2-(Hydroxymethyl)-1H-indole;1H-Indole-2-methanol 90%;1H-Indole-2-methanol
CAS:24621-70-3
MF:C9H9NO
MW:147.17
EINECS:
Product Categories:Heterocyclic Compounds
Mol File:24621-70-3.mol
1H-Indol-2-ylmethanol Structure
1H-Indol-2-ylmethanol Chemical Properties
Melting point 72-78 °C
Boiling point 360.6±17.0 °C(Predicted)
density 1.272±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form solid
pka14.86±0.10(Predicted)
AppearanceLight brown to yellow Solid
InChIInChI=1S/C9H9NO/c11-6-8-5-7-3-1-2-4-9(7)10-8/h1-5,10-11H,6H2
InChIKeyXEEANGGQJOWRTG-UHFFFAOYSA-N
SMILESN1C2=C(C=CC=C2)C=C1CO
Safety Information
Hazard Codes Xi
Risk Statements 41
Safety Statements 26
WGK Germany 3
HS Code 2933998090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Dam. 1
MSDS Information
1H-Indol-2-ylmethanol Usage And Synthesis
UsesReactant for the synthesis of:
  • Oxazino[4,3-a]indoles
  • 2-arylsulfonylmethyl-3-piperazinylmethylindole derivatives as 5-HT6 receptor ligands
  • SR13668 designed to mimic the unique anticancer mechanisms of dietary indole-3-carbinol to block Akt signaling
  • Azido- and isothiocyanato-substituted indoles as melatoninergic agents
SynthesisPut 20kg of 4-oxoindole, 4kg of Pd/C catalyst with 5% Pd content (palladium carbon catalyst) and 60L of diethylene glycol dimethyl ether as solvent into a 100L reactor with stirring device, and then heat up the reactor with steam, turn on the stirring, and carry out catalytic dehydrogenation reaction under the condition of T=150~160C. After the dehydrogenation reaction, filter it and separate out the Pd/C catalyst, which can be used for recycling. After the dehydrogenation reaction, filtration, separation of the Pd/C catalyst, separated from the Pd/C catalyst can be recycled, the separation of the filtrate pumped to 100L distillation kettle, distillation under reduced pressure, collection of diethylene glycol dimethyl ether fraction (can continue to use), and then collect the product of 2-methylhydroxyindole fraction of 11kg, the mass yield of 55%, content: 99.0%.
Tag:1H-Indol-2-ylmethanol(24621-70-3) Related Product Information
1-Methylindole-2-carboxylic acid Indole-2-carboxylic acid 5-Fluoroindole-2-carboxylic acid 3-HYDROXYINDOLE-2-CARBOXYLIC ACID METHYL ESTER Ethyl 5-hydroxyindole-2-carboxylate ETHYL 5,6-DIMETHOXYINDOLE-2-CARBOXYLATE 5-Hydroxyindole-2-carboxylic acid 5,6-DIMETHOXYINDOLE-2-CARBOXYLIC ACID 5-Chloroindole-2-carboxylic acid Ethyl 5-Bromoindole-2-carboxylate 1H-INDOL-2-YLMETHANOL Ethyl indole-2-carboxylate 5-Bromoindole-2-carboxylic acid Ethyl 5-chloro-2-indolecarboxylate 5-Methoxyindole-2-carboxylic acid Ethyl 5-methylindole-2-carboxylate Ethyl 5-benzyloxyindole-2-carboxylate 2,3-Dihydro-1H-indol-2-ylmethanol