135285-98-2

Basic information

• Product Name: (S)-2-PHENYL-2-PHENYLAMINO-ETHANOL
• Synonyms: (S)-2-PHENYL-2-PHENYLAMINO-ETHANOL
• CAS NO: 135285-98-2
• Molecular Formula: C₁₄H₁₅NO
• Molecular Weight: 213.27
• Product Categories: pharmacetical
• Mol File: 135285-98-2.mol
• Article Data: 150

Chemical Properties

• Boiling Point: 376.2°Cat760mmHg
• Flash Point: 146.8°C
• Appearance: /
• Density: 1.156g/cm³
• Vapor Pressure: 2.51E-06mmHg at 25°C
• Refractive Index: 1.641
• PKA: 14.18±0.10(Predicted)
• CAS DataBase Reference: (S)-2-PHENYL-2-PHENYLAMINO-ETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-PHENYL-2-PHENYLAMINO-ETHANOL(135285-98-2)
• EPA Substance Registry System: (S)-2-PHENYL-2-PHENYLAMINO-ETHANOL(135285-98-2)

Safety Data

• Hazardous Substances Data: 135285-98-2(Hazardous Substances Data)

Usage

General Description

(S)-2-Phenyl-2-phenylamino-ethanol is a chemical compound with a molecular formula of C16H17NO and a molar mass of 239.31 g/mol. It is a chiral compound with two enantiomers, (S)- and (R)-2-phenyl-2-phenylamino-ethanol. (S)-2-PHENYL-2-PHENYLAMINO-ETHANOL has a hydroxyl group and an amino group attached to a carbon atom, and it has a phenyl group attached to the alpha carbon. It is commonly used as a synthetic intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. It may also have applications in research and development as a building block for the synthesis of various organic molecules. Additionally, it may have potential applications as a chiral auxiliary in asymmetric synthesis.

InChI:InChI=1/C14H15NO/c16-11-14(12-7-3-1-4-8-12)15-13-9-5-2-6-10-13/h1-10,14-16H,11H2/t14-/m1/s1

Upstream product

• 55552-57-3 C₁₄H₁₄BrHgN 
• 1333483-14-9 N-methyll-N-(phenylethylnyl)methanesulfonamide 
• 1333483-22-9 N-phenyl-N-(phenylethylnyl)methanesulfonamide 
• 201024-81-9 C,N-diphenylnitrone 
• 100-42-5 styrene 
• 96-09-3 styrene oxide 
• 98-95-3 nitrobenzene 
• 62-53-3 aniline 
• 100-52-7 benzaldehyde 
• 109-87-5 Dimethoxymethane 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 536-74-3 phenylacetylene 
• 1333483-40-1 N-benzyl-N-(methylsulfonyl)-2-phenyl-2-(phenylamino)acetamide 
• 1333483-39-8 N-(methylsulfonyl)-N,2-diphenyl-2-(phenylamino)acetamide 

Downstream Products

• 119492-43-2 (R)-2-Phenyl-2-(phenylamino)ethanol 

Relevant articles and documents

Kinetic resolution ofN-aryl β-amino alcoholsviaasymmetric aminations of anilines

An efficient kinetic resolution ofN-aryl β-amino alcohols has been developedviaasymmetricpara-aminations of anilines with azodicarboxylates enabled by chiral phosphoric acid catalysis. Broad substrate scope and high kinetic resolution performances were afforded with this method. Control experiments supported the critical roles of the NH and OH group in these reactions.

A novel copper framework with amino tridentate N-donor ligand as heterogeneous catalyst for ring opening of epoxides

A novel metal–organic framework (MOF) [Cu3L(2,6-NDC)2]·0.5DMF (MOF-Cu-1) was synthesized by solvothermal reaction of copper nitrate trihydrate with 2,6-naphthalenedicarboxylic acid (2,6-H2NDC) and amino tridentate N-donor

Air-stable Organoantimony (III) Perfluoroalkyl(aryl)sulfonate complexes as highly efficient, selective, and recyclable catalysts for C–C and C–N bond-forming reactions

A series of air-stable organoantimony (III) perfluoroalkyl(aryl)sulfonate complexes with an azastibocine framework {t-BuN(CH2C6H4)2SbOSO2C4F9 (2a); [t-BuN(CH2C6/