240423-53-4

Basic information

• Product Name: (1S,2R)-2-[N-BENZYL-N-(MESITYLENESULFONYL)AMINO]-1-PHENYLPROPYL ACETATE
• Synonyms: ACTIC ACID (1S,2R)-2-[N-BENZYL-N-(MESITYLENESULFONYL)AMINO]-1-PHENYLPROPYL ESTER;ACETIC ACID (1S,2R)-2-[N-BENZYL-N-(MESITYLENESULFONYL)AMINO]-1-PHENYLPROPYL ESTER;(1S,2R)-2-[N-BENZYL-N-(MESITYLENESULFONYL)AMINO]-1-PHENYLPROPYL ACETATE;(1S,2R)-N-BENZYL-N-(MESITYLENESULFONYL)-O-ACETYLNOREPHEDRINE;Acetic Acid (1S,2R)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenylpropyl Ester [Reagent for double aldol reaction];(1S,2R)-N-Benzyl-N-(mesitylenesulfonyl)-O-acetylnorephedrine (1S,2R)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenylpropyl Acetate;N-[(1R,2S)-2-(Acetyloxy)-1-methyl-2-phenylethyl]-2,4,6-trimethyl-N-(phenylmethyl)benzenesulfonamide;(1S,2R)-2-(N-Benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl acetate
• CAS NO: 240423-53-4
• Molecular Formula: C27H31NO4S
• Molecular Weight: 465.6
• Product Categories: Asymmetric Synthesis;Synthetic Organic Chemistry
• Mol File: 240423-53-4.mol
• Article Data: 0

Chemical Properties

• Melting Point: 121 °C
• Boiling Point: 605.617°C at 760 mmHg
• Flash Point: 320.066°C
• Appearance: /
• Density: 1.176g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.583
• PKA: -7.02±0.70(Predicted)
• CAS DataBase Reference: (1S,2R)-2-[N-BENZYL-N-(MESITYLENESULFONYL)AMINO]-1-PHENYLPROPYL ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R)-2-[N-BENZYL-N-(MESITYLENESULFONYL)AMINO]-1-PHENYLPROPYL ACETATE(240423-53-4)
• EPA Substance Registry System: (1S,2R)-2-[N-BENZYL-N-(MESITYLENESULFONYL)AMINO]-1-PHENYLPROPYL ACETATE(240423-53-4)

Safety Data

• Hazardous Substances Data: 240423-53-4(Hazardous Substances Data)

Usage

General Description

(1S,2R)-2-[N-BENZYL-N-(MESITYLENESULFONYL)AMINO]-1-PHENYLPROPYL ACETATE is a chemical compound with a complex structure, consisting of a benzylic group, a mesitylenesulfonyl amino group, and a phenylpropyl acetate group. It is a chiral compound, with a stereocenter at the first carbon atom and the second carbon atom, giving it two possible enantiomers. (1S,2R)-2-[N-BENZYL-N-(MESITYLENESULFONYL)AMINO]-1-PHENYLPROPYL ACETATE is commonly used in organic synthesis and medicinal chemistry research due to its ability to serve as a chiral auxiliary and as a building block for the synthesis of various pharmaceuticals and biologically active molecules. It has potential applications in the development of new drugs and as a tool in the study of asymmetric synthesis.

InChI:InChI=1/C27H31NO4S/c1-19-16-20(2)27(21(3)17-19)33(30,31)28(18-24-12-8-6-9-13-24)22(4)26(32-23(5)29)25-14-10-7-11-15-25/h6-17,22,26H,18H2,1-5H3/t22-,26-/m1/s1