(1-Methyl-1H-indol-2-yl)-methanol

(1-Methyl-1H-indol-2-yl)-methanol Suppliers list
Company Name: Shanghai Boyners Pharm-Tech Co., Ltd.  
Tel: 13817873692
Email: mkt@boynerspharm.com
Company Name: ShangHai Wisacheam Pharmaceutical Co., Ltd.  
Tel: 13817485796
Email: tim@wisacheampharm.com
Company Name: JW & Y Pharmlab Co., Ltd.  
Tel: 021-64340559
Email: xinyu_shi@jwypharmlab.com.cn
Company Name: Shanghai Chenzhu Pharmaceutical Co., Ltd.  
Tel: 13162380607
Email: 1696175688@qq.com
Company Name: Amadis Chemical Company Limited  
Tel: 571-89925085
Email: sales@amadischem.com
(1-Methyl-1H-indol-2-yl)-methanol Basic information
Product Name:(1-Methyl-1H-indol-2-yl)-methanol
Synonyms:(1-methyl-2-indolyl)methanol;RARECHEM AL BD 0864;(1-methylindol-2-yl)methanol;1H-Indole-2-methanol, 1-methyl-;2-(Hydroxymethyl)-1-methylindole;1-methyl-1H-Indole-2-methanol;(1-Methyl-1H-indol-2-yl)-methanol
CAS:1485-22-9
MF:C10H11NO
MW:161.2
EINECS:
Product Categories:
Mol File:1485-22-9.mol
(1-Methyl-1H-indol-2-yl)-methanol Structure
(1-Methyl-1H-indol-2-yl)-methanol Chemical Properties
Melting point 108-110 °C(Solv: benzene (71-43-2))
Boiling point 120 °C(Press: 0.05 Torr)
density 1.12±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka14.89±0.10(Predicted)
AppearanceOff-white to light yellow Solid
Safety Information
Risk Statements 41
Safety Statements 26-39
MSDS Information
(1-Methyl-1H-indol-2-yl)-methanol Usage And Synthesis
Uses1-Methylindole-2-methanol is a reagent used in the synthesis of peroxisome proliferator activated receptors, PPARα and PPARγ partial agonists in the treatment of type 2 diabetes.
(1-Methyl-1H-indol-2-yl)-methanol Preparation Products And Raw materials
Tag:(1-Methyl-1H-indol-2-yl)-methanol(1485-22-9) Related Product Information
methyl 1-methyl-1H-indole-2-carboxylate 1-Methylindole-2-carboxylic acid Ethyl 1-(4-chlorobenzyl)-3-(1H-pyrrol-1-yl)-1H-indole-2-carboxylate 1-Phenyl-1H-indole-2-carboxylic acid 5-Methoxy-1-methyl-1H-indole-2-carboxylic acid CHEMBRDG-BB 5280909 N-Benzylnaltrindole hydrochloride 1-Phenylmethyl-1H-indole-2-methanol 5-Benzyloxy-1-methyl-1H-indole-2-carboxylic acid Ethyl 1-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]-3-phenyl-1H-indole-2-carboxylate Ethyl 1-benzyl-3-(1H-pyrrol-1-yl)-1H-indole-2-carboxylate Ethyl 1-(4-methylbenzyl)-3-(1H-pyrrol-1-yl)-1H-indole-2-carboxylate Ethyl 1-(2-chlorobenzyl)-3-(1H-pyrrol-1-yl)-1H-indole-2-carboxylate Ethyl 1-(3-chlorobenzyl)-3-(1H-pyrrol-1-yl)-1H-indole-2-carboxylate Ethyl 1-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]-3-(1H-pyrrol-1-yl)-1H-indole-2-carboxylate Ethyl 1-(2,4-dichlorobenzyl)-3-((2,4-dichlorobenzyl)[3-(trifluoromethyl)benzoyl]amino)-1H-indole-2-carboxylate 1-(beta-Dimethylaminoaethyl)-2-methoxycarbonyl-3-isopropyloxy-5-methyl -indol-hydrochlorid 1-(beta-Dimethylaminoaethyl)-2-ethoxycarbonyl-3-ethoxy-6-chlor-indol-t oluol-4-sulfonat