300345-76-0

Basic information

• Product Name: (1S,2S)-N-Methylsulfonyl-1,2-diphenylethanediamine, 98+%
• Synonyms: (1S,2S)-N-Methylsulfonyl-1,2-diphenylethanediamine, 98+%;N-[(1S,2S)-2-Amino-1,2- diphenylethyl]methanesulfonamide,99%e.e.;(1S,2S)-N-Methylsulfonyl-1,2-diphenylethanediamine
• CAS NO: 300345-76-0
• Molecular Formula: C₁₅H₁₈N₂O₂S
• Molecular Weight: 290.38062
• Mol File: 300345-76-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 118-120°C
• Appearance: /
• Sensitive: Air Sensitive
• CAS DataBase Reference: (1S,2S)-N-Methylsulfonyl-1,2-diphenylethanediamine, 98+%(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-N-Methylsulfonyl-1,2-diphenylethanediamine, 98+%(300345-76-0)
• EPA Substance Registry System: (1S,2S)-N-Methylsulfonyl-1,2-diphenylethanediamine, 98+%(300345-76-0)

Safety Data

• RIDADR: UN3259
• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 300345-76-0(Hazardous Substances Data)

Usage

General Description

"(1S,2S)-N-Methylsulfonyl-1,2-diphenylethanediamine, 98+%" is a chemical compound with a purity of 98% or higher. It is a diamine compound containing a methylsulfonyl group and two phenyl groups. The compound has a stereochemistry of (1S,2S), indicating the specific arrangement of atoms in space. It is commonly used as a reagent in organic synthesis, particularly in the production of chiral ligands and catalysts. (1S,2S)-N-Methylsulfonyl-1,2-diphenylethanediamine, 98+% is known for its use in asymmetric hydrogenation and other reactions that require enantiomerically pure compounds. Its high purity makes it a valuable tool in the development of pharmaceuticals and other fine chemicals.

Upstream product

• 29841-69-8 (S,S)-1,2-diphenyl-1,2-diaminoethane 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 1295509-72-6 C₃₆H₄₁N₅O₃S₂ 
• 1352614-15-3 N-((1S,2S)-2-(3-((1R)-(6-methoxyquinolin-4-yl)((2R,4S,5R)-5-vinylquinuclidin-2-yl)methyl)thioureido)-1,2-diphenylethyl)methanesulfonamide 
• 1353719-77-3 N-((1S,2S)-2-(3-((S)-3,3-dimethyl-1-(pyrrolidin-1-yl)butan-2-yl)thioureido)-1,2-diphenylethyl)methanesulfonamide 
• 1360897-47-7 N-((1S,2S)-1,2-diphenyl-2-(2-(tetrahydro-2H-pyran-2-yloxy)ethylamino)ethyl)methanesulfonamide 
• 1360897-48-8 N-((1S,2S)-2-(2-hydroxyethylamino)-1,2-diphenylethyl)methanesulfonamide 
• 1245811-48-6 tethered (S,S)-MsDPEN 
• 1404469-27-7 N-((1S,2S)-2-(4-(4-methylcyclohexa-1,4-dienyl)butylamino)-1,2-diphenylethyl)methanesulfonamide 
• 1404469-32-4 N-((1S,2S)-2-(4-(5-methylcyclohexa-1,4-dienyl)butylamino)-1,2-diphenylethyl)methanesulfonamide 
• 1404469-38-0 N-((1S,2S)-2-(4-(4-methylcyclohexa-1,4-dienyl)butylamino)-1,2-diphenylethyl)methanesulfonamide hydrochloride 
• 1404469-40-4 N-((1S,2S)-2-(4-(5-methylcyclohexa-1,4-dienyl)butylamino)-1,2-diphenylethyl)methanesulfonamide hydrochloride 

Relevant articles and documents

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METHOD FOR THE PREPARATION OF TRICYCLIC AMINO ALCOHOL DERIVATIVES THROUGH AZIDES

The present invention is directed to processes for the preparation of a tricyclic amino-alcohol derivative useful for treating and preventing diabetes, obesity, hyperlipidemia and the like, which compound is represented by the formula (1): wherein R1 represents a lower alkyl group or a benzyl group; *1 represents an asymmetric carbon atom; R2 represents a hydrogen atom, a halogen atom or a hydroxyl group; and A represents one of the following groups: wherein X represents NH, O or S; R5 represents a hydrogen atom, a hydroxyl group, an amino group or an acetylamino group; and *2 represents an asymmetric carbon atom when R5 is not a hydrogen atom. The processes of the present invention proceed via azide derivatives and are convenient, practical preparing processes with low cost which comprise a small number of steps with good industrial work efficiency.