14467-53-9

Basic information

• Product Name: Benzenemethanol, a-[[(1-methylethyl)amino]methyl]-,(aS)-
• Synonyms: Benzenemethanol,a-[[(1-methylethyl)amino]methyl]-,(S)-; Benzyl alcohol, a-[(isopropylamino)methyl]-, L-(+)- (8CI); TV 696
• CAS NO: 14467-53-9
• Molecular Formula: C11H17 N O
• Molecular Weight: 179.262
• Mol File: 14467-53-9.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, a-[[(1-methylethyl)amino]methyl]-,(aS)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-[[(1-methylethyl)amino]methyl]-,(aS)-(14467-53-9)
• EPA Substance Registry System: Benzenemethanol, a-[[(1-methylethyl)amino]methyl]-,(aS)-(14467-53-9)

Safety Data

• Hazardous Substances Data: 14467-53-9(Hazardous Substances Data)

Upstream product

• 96-09-3 styrene oxide 
• 75-31-0 isopropylamine 
• 71065-28-6 1R,2S,5R-(-)-8-phenylmenthyl mandelate 
• 7322-88-5 (S)-acetylmandelic acid 
• 17199-29-0 (S)-Mandelic acid 
• 40435-14-1 (S)-1-phenyl-2-(tosyloxy)ethanol 
• 122-78-1 phenylacetaldehyde 
• 20780-54-5 (S)-styrene oxide 
• 25779-13-9 (S)-1-phenyl-1,2-ethanediol 
• 124817-06-7 (S)-2-azido-1-phenylethanol 
• 67-64-1 acetone 
• 56613-81-1 (S)-2-Amino-1-phenyl-1-ethanol 
• 91850-94-1 2-(isopropylimino)-1-phenylethanone 
• 89843-14-1 2-hydroxy-N-isopropyl-2-phenylacetamide 

Downstream Products

• 4164-21-0 2-(isopropylamino)-1-phenylethanol 
• 1460197-46-9 N-(2-{[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy}-2-phenylethyl)propan-2-amine 
• 1415504-56-1 2-{[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl](isopropyl)amino}-1-phenylethanol 
• 1078-35-9 N-(2-chloro-2-phenylethyl)isopropylammonium chloride 
• 2027-65-8 1-(1-methylethyl)-3-phenyl-2-azetidinone 
• 4164-23-2 1-isopropyl-2-phenyl-aziridine 
• 116203-87-3 N-nitroso-2-isopropylamino-1-phenylethanol 
• 25244-11-5 2-(isopropyl-methyl-amino)-1-phenyl-ethanol 

Relevant articles and documents

Efficient Synthesis of 2-Amino-1-Arylethanols Through a Lewis Base-Catalyzed SiCl4-Mediated Asymmetric Passerini-Type Reaction

We herein report, a practical and efficient strategy for the synthesis of enantiomerically enriched 2-amino-1-arylethanols, a structural motif commonly encountered in the family of β-adrenergic blockers or agonists, through a Lewis base-catalyzed SiClsub

2-Aryl-2-hydroxyethylamine substituted 4-oxo-4,7-dihydrothieno[2,3-b]pyridines as broad-spectrum inhibitors of human herpesvirus polymerases

A novel series of 2-aryl-2-hydroxyethylamine substituted 4-oxo-4,7-dihydrothieno[2,3-b]pyridine-5-carboxamides have been identified as potent antivirals against human herpesviruses. These compounds demonstrate broad-spectrum inhibition of the herpesvirus polymerases HCMV, HSV-1, EBV, and VZV with high specificity compared to human DNA polymerases.

Preparation of phenolic chiral crown ethers and podands and their enantiomer recognition ability toward secondary amines

Phenolic pseudo-24-crown-8 (S,S)-3, pseudo-27-crown-9 (S,S)-4, and podands (R,R)-5 and (R,R)-6 possessing phenyl groups as chiral barriers were prepared and their chiral recognition properties toward secondary neutral amines were examined. Pseudo-24-crown-8 (S,S)-3 and podand (R,R)-5 showed sufficient binding ability and moderate chiral recognition ability toward secondary amines.