2-(2-Aminophenyl)propan-2-ol

2-(2-Aminophenyl)propan-2-ol Suppliers list
Company Name: Adamas Reagent, Ltd.  
Tel: 400-6009262 15618770481
Email: yhx@titansci.com
Company Name: Xiamen Dano Pharmaceutical Co., LTD(China)  
Tel: 0592-6266840 15750707980;
Email: chemdano@126.com
Company Name: ZHEJIANG ZETIAN FINE CHEMICALS CO.,LTD  
Tel: 0571-87322520 18957127338
Email: sales@zetchem.com
Company Name: Shanghai Rlavie Technology Co., Ltd.  
Tel: 021-67759270 17717059219
Email: sales@rlavie.com
Company Name: Aikon International Limited  
Tel: 025-58859352 15955137747
Email: sales01@aikonchem.com

2-(2-Aminophenyl)propan-2-ol manufacturers

2-(2-Aminophenyl)propan-2-ol Basic information
Product Name:2-(2-Aminophenyl)propan-2-ol
Synonyms:o-aminophenyldimethylcarbinol;Nsc76547;2-Amino-alpha,alpha-dimethylbenzenemethanol;alhpa,alpha-Dimethyl-2-aminobenzyl alcohol;alpha,alpha-Dimethyl-o-aminobenzyl alcohol;o-Amino-alpha,alpha-dimethylbenzyl alcohol;2-AMINO-ALPHA,ALPHA-DIMETHYLBENZYL ALCOHOL;benzenemethanol, 2-amino-alpha,alpha-dimethyl-
CAS:15833-00-8
MF:C9H13NO
MW:151.21
EINECS:
Product Categories:Benzhydrols, Benzyl & Special Alcohols
Mol File:15833-00-8.mol
2-(2-Aminophenyl)propan-2-ol Structure
2-(2-Aminophenyl)propan-2-ol Chemical Properties
Boiling point 289℃
density 1.084
Fp 129℃
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka14.35±0.29(Predicted)
AppearanceColorless to light yellow Viscous Liquid
Safety Information
HazardClass IRRITANT
MSDS Information
2-(2-Aminophenyl)propan-2-ol Usage And Synthesis
Synthesis
Methylmagnesium Bromide

75-16-1

2-Aminoacetophenone

551-93-9

2-(2-AMINOPHENYL)PROPAN-2-OL

15833-00-8

GENERAL STEPS: 1-(2-aminophenyl)ethanone (1.50 g, 11.1 mmol) was dissolved in tetrahydrofuran (11 mL) under argon protection and cooled at 0 °C. Subsequently, methylmagnesium bromide (1.0 mol/L tetrahydrofuran solution, 11.1 mL, 11.1 mmol) was added slowly. After addition, the reaction mixture was gradually warmed to room temperature and stirred. Upon completion of the reaction, the reaction was carefully quenched with saturated aqueous ammonium chloride solution. The reaction mixture was extracted with ethyl acetate (3 x 20 mL), the organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product obtained was a brown oil, which was purified by fast column chromatography to give 2-(2-aminophenyl)propan-2-ol as a light-colored oil (1.20 g, 72% yield).LC-MS analysis showed a retention time of 0.24 min, and m/z 134 ([M-OH]-) was observed in ESI+ mode.1H NMR (400 MHz, chloroform-d) δ ( ppm): 7.15 (d, 1H), 7.06 (t, 1H), 6.72 (t, 1H), 6.65 (d, 1H), 3.65 (br s, 1H), 1.67 (s, 6H).

References[1] Patent: WO2018/17490, 2018, A1. Location in patent: Paragraph 0163; 0164
[2] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 1, p. 189 - 192
[3] Organic and Biomolecular Chemistry, 2015, vol. 13, # 47, p. 11486 - 11491
2-(2-Aminophenyl)propan-2-ol Preparation Products And Raw materials
Raw materialsMethylmagnesium Bromide-->Methyl anthranilate-->2-Aminoacetophenone
Tag:2-(2-Aminophenyl)propan-2-ol(15833-00-8) Related Product Information
ETHYL 3-HYDROXY-4,6-DIMETHOXY-2-OXOINDOLINE-3-CARBOXYLATE 3-HYDROXY-3-PHENYLOXINDOLE 3-hydroxy-3-acetonyl-2-oxindole 3-Hydroxy-5-methyl-2-oxo-3-trifluoromethylindoline 3-Allyl-3-hydroxy-1,3-dihydro-indol-2-one 3-Hydroxy-5-methoxy-2-oxo-3-(trifluoromethyl)indoline 5-Bromo-3-[2-(4-bromophenyl)-2-oxoethyl]-3-hydroxy-1,3-dihydro-2H-indol-2-one 3-Hydroxy-1-methyl-3-(2-oxo-propyl)-1,3-dihydro-indol-2-one 5-Bromo-3-hydroxy-3-[2-(4-methoxyphenyl)-2-oxoethyl]-1,3-dihydro-2H-indol-2-one TIMTEC-BB SBB000849 AKOS BC-1617 AKOS BC-3082 6-CHLORO-3-HYDROXY-2-OXO-3-(TRIFLUOROMETHYL)INDOLINE 1-(2-CHLORO-ETHYL)-3-HYDROXY-3-(2-OXO-PROPYL)-1,3-DIHYDRO-INDOL-2-ONE 3-hydroxy-3-(2-oxo-2-phenylethyl)-1,3-dihydro-2H-indol-2-one 1-METHYL-2-OXO-3-(2-OXOPROPYL)-2,3-DIHYDRO-1H-INDOL-3-YL ACETATE AKOS BC-1538 3-[2-(4-bromophenyl)-2-oxoethyl]-3-hydroxy-1,3-dihydro-2H-indol-2-one