114663-05-7

Basic information

• Product Name: (±)-N-(2-hydroxy-1-phenylethyl)-4-methylbenzenesulfonamide
• CAS NO: 114663-05-7
• Molecular Weight: 291.371
• Mol File: 114663-05-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: (±)-N-(2-hydroxy-1-phenylethyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: (±)-N-(2-hydroxy-1-phenylethyl)-4-methylbenzenesulfonamide(114663-05-7)
• EPA Substance Registry System: (±)-N-(2-hydroxy-1-phenylethyl)-4-methylbenzenesulfonamide(114663-05-7)

Safety Data

• Hazardous Substances Data: 114663-05-7(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 144-86-5 N-chloro-4-methylbenzenesulfonamide 
• 96-09-3 styrene oxide 
• 70-55-3 toluene-4-sulfonamide 
• 98-59-9 p-toluenesulfonyl chloride 
• 20989-17-7 Phenylglycinol 
• 1049016-44-5 N-(2-pivaloyloxy-1-phenylethyl)-4-toluenesulfonamide 
• 918943-73-4 2-((4-methylphenyl)sulfonamido)-2-phenylethyl benzoate 
• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 24395-14-0 N-(p-tolylsulfonyl)-2-phenylaziridine 
• 51608-60-7 phenyl N-tosyl imine 

Downstream Products

• 114663-08-0 4-Methyl-N-phenylsulfanyl-N-[1-phenyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-benzenesulfonamide 

Relevant articles and documents

Introduction of Functionalized C1, C2, and C3 Units to Imines through the Dimethylzinc-Air-Initiated Radical Addition

Introduction of functionalized C1, C2, and C3 units to imines was achieved by using the dimethylzinc-air-initiated α-alkoxyalkyl radical addition as a key reaction. The addition to a C= N double bond chemoselectively occurred in the presence of a C=O doub

A tandem process for the synthesis of β-aminoboronic acids from aziridines with haloamine intermediates

An unprecedented synthetic strategy is devised to generate β-aminoboronic acids from aziridines via a sequential process involving 1,2-iodoamine formation and radical borylation under light irradiation. A variety of aziridines including multiply substituted aziridines have been successfully employed as synthetic precursors, expanding their synthetic utility compared to previous methods. Mechanistic studies suggest that the boron source plays a unique role in the borylation step, and in the formation of haloamine intermediates.

A One-Pot Reaction toward the Diastereoselective Synthesis of Substituted Morpholines

The diastereoselective synthesis of various substituted morpholines has been achieved from vinyloxiranes and amino-alcohols under sequential Pd(0)-catalyzed Tsuji-Trost/Fe(III)-catalyzed heterocyclization. Using the same strategy, 2,6-, 2,5-, and 2,3-disubstituted as well as 2,5,6- and 2,3,5-trisubstituted morpholines were obtained in good to excellent yields and diastereoselectivities.

Efficient and regioselective ring-opening of arylaziridines with alcohols, thiols, amines and N-heteroaromatic compounds using sulphated zirconia

Sulphated zirconia is an efficient catalyst for the regioselective ring-opening of aryl-substituted aziridines. This heterogeneous catalyst can be used several times without loss of activity and is compatible with a variety of acid sensitive and slightly basic nucleophiles.