ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Indole Compounds >5-Hydroxy-2-methylindole

5-Hydroxy-2-methylindole

5-Hydroxy-2-methylindole Suppliers list
Company Name: Henan SIWEIYIN Medicines Co., Ltd.  Gold
Tel: 13072124697 18837373888
Email: zhanghyoffer@163.com
Company Name: Shanghai Synteam Biochem CO.,ltd  Gold
Tel: +86-021-58380978 13482386415
Email: info@systeambc.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: Beijing HwrkChemical Technology Co., Ltd  
Tel: 89508211 18501085097
Email: sales.bj@hwrkchemical.com

5-Hydroxy-2-methylindole manufacturers

5-Hydroxy-2-methylindole Basic information
Product Name:5-Hydroxy-2-methylindole
Synonyms:5-HYDROXY-2-METHYLINDOLE;2-Methyl-5-Indanone;5-Hydroxy-2-Methyl-1H-indole;1H-Indol-5-ol,2-Methyl-;5-Hydroxy-2-methylindol;5-Hydroxy-2-methyL;5-Hydroxy-2-methylindole,98%;2-METHYL-1H-INDOL-5-OL
CAS:13314-85-7
MF:C9H9NO
MW:147.17
EINECS:236-345-0
Product Categories:pharmacetical;Indoles;Indoles and derivatives
Mol File:13314-85-7.mol
5-Hydroxy-2-methylindole Structure
5-Hydroxy-2-methylindole Chemical Properties
Melting point 130-132℃
Boiling point 344.8±22.0 °C(Predicted)
density 1.262±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
form Solid
pka10.05±0.40(Predicted)
color Brown
Sensitive Light Sensitive
CAS DataBase Reference13314-85-7(CAS DataBase Reference)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HS Code 29339900
MSDS Information
5-Hydroxy-2-methylindole Usage And Synthesis
Application5-Hydroxy-2-methylindole is a useful research chemical.
Synthesis
5-METHOXY-2-METHYLINDOLE

1076-74-0

5-Hydroxy-2-methylindole

13314-85-7

The general procedure for the synthesis of 5-hydroxy-2-methylindole from 5-methoxy-2-methylindole was as follows: a solution of boron tribromide (32.5 mL, 341 mmol) in dichloromethane (60 mL) was added batchwise to a solution of 5-methoxy-2-methylindole (25 g, 155 mmol) in dichloromethane (250 mL) that had been cooled to -50 °C. After stirring the reaction mixture at -30 °C for 15 min, it was slowly warmed to room temperature and stirring was continued for 1 hour. Subsequently, dichloromethane (300 mL) was added in batches and the reaction mixture was cooled to 0 °C. Water was slowly added and the pH of the mixture was adjusted to 6 with 4N sodium hydroxide solution. the organic layer was separated and the aqueous layer was extracted with dichloromethane. All organic layers were combined, washed sequentially with water and saturated brine and dried over anhydrous magnesium sulfate. The solvent was removed by evaporation under reduced pressure and the resulting crude product was purified by column chromatography with the eluent ethyl acetate/dichloromethane (initial ratio 1:9, subsequently adjusted to 15:85) to give 5-hydroxy-2-methylindole (21.2 g, 93% yield) as a white solid.

References[1] European Journal of Medicinal Chemistry, 2013, vol. 63, p. 578 - 588
[2] Patent: US2003/212055, 2003, A1
[3] Journal of Medicinal Chemistry, 2012, vol. 55, # 5, p. 1940 - 1956
[4] Research on Chemical Intermediates, 2010, vol. 36, # 8, p. 975 - 983
[5] Bioorganic and medicinal chemistry, 2004, vol. 12, # 17, p. 4685 - 4700
5-Hydroxy-2-methylindole Preparation Products And Raw materials
Raw materials5-Methoxy-2-methylindole-->Boron tribromide-->Water-->Dichloromethane
Preparation Products5-isopropoxy-2-methyl-1H-indole
Tag:5-Hydroxy-2-methylindole(13314-85-7) Related Product Information
Hydroxy silicone oil 3-Methylindole 2,3,4-Trihydroxybenzoic acid Methyl salicylate Methyl acetate Kresoxim-methyl L-5-Hydroxytryptophan 4-Ethyl-5-fluoro-6-hydroxypyrimidine 5-Hydroxyindole 4-Hydroxybenzoic acid Hydroxyapatite 2-Methylindole Glycolic acid Methylparaben Tribenuron methyl Thiophanate-methyl Chlorophosphonazo III Metsulfuron methyl