13638-89-6

Basic information

• Product Name: MESO-2,3-DIPHENYL-SUCCINIC ACID DIETHYL ESTER
• Synonyms: MESO-2,3-DIPHENYL-SUCCINIC ACID DIETHYL ESTER
• CAS NO: 13638-89-6
• Molecular Formula: C₂₀H₂₂O₄
• Molecular Weight: 326.39
• Mol File: 13638-89-6.mol
• Article Data: 4

Chemical Properties

• Melting Point: 139-140.5 °C
• Boiling Point: 418.6°C at 760 mmHg
• Flash Point: 202.5°C
• Appearance: /
• Density: 1.123g/cm³
• Vapor Pressure: 3.25E-07mmHg at 25°C
• Refractive Index: 1.543
• CAS DataBase Reference: MESO-2,3-DIPHENYL-SUCCINIC ACID DIETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: MESO-2,3-DIPHENYL-SUCCINIC ACID DIETHYL ESTER(13638-89-6)
• EPA Substance Registry System: MESO-2,3-DIPHENYL-SUCCINIC ACID DIETHYL ESTER(13638-89-6)

Safety Data

• Hazardous Substances Data: 13638-89-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C20H22O4/c1-3-23-19(21)17(15-11-7-5-8-12-15)18(20(22)24-4-2)16-13-9-6-10-14-16/h5-14,17-18H,3-4H2,1-2H3/t17-,18+

Upstream product

• 101-97-3 Ethyl 2-phenylethanoate 
• 4870-65-9 2-bromophenylacetic acid 
• 611-71-2 MANDELIC ACID 
• 2882-19-1 ethyl 2-phenyl-2-bromoacetate 
• 75-03-6 ethyl iodide 
• 64-17-5 ethanol 
• 151-50-8 potassium cyanide 
• 7584-72-7 meso-2,3-diphenylsuccinic acid 
• 103-82-2 phenylacetic acid 
• 865-47-4 potassium tert-butylate 
• 2303-76-6 sodium diethyl phosphite 
• 71-43-2 benzene 
• 129320-23-6 meso-2.3-diphenyl-succinic acid-dichloride 

Downstream Products

• 131252-50-1 meso-1,4-diiodo-2,3-diphenyl-butane 
• 21037-34-3 (2R₃R)-2,3-Diphenylbernsteinsaeure 
• 74431-38-2 (2S,3S)-(+)-2,3-Diphenylsuccinic acid 
• 7584-72-7 meso-2,3-diphenylsuccinic acid 
• 1225-13-4 (2S,3S)-(dl)-2,3-diphenylsuccinic acid 
• 6287-98-5 meso-2,3-bis-(4-nitro-phenyl)-succinic acid diethyl ester 
• 6583-62-6 (2R,3S)-2,3-diphenylbutane-1,4-diol 
• 286936-47-8 N-(α-Methylbenzyl)-3,4-diphenylpyrrolidin-2,5-dione 
• 4209-77-2 N-Benzyl-3,4-diphenylpyrrolidine 
• 1225-13-4 erythro-2,3-diphenylsuccinic acid 
• 1225-13-4 threo-2,3-diphenylsuccinic acid 

Relevant articles and documents

Dynamic kinetic resolution of bis-aryl succinic anhydrides: Enantioselective synthesis of densely functionalised γ-butyrolactones

The efficient Dynamic Kinetic Resolution (DKR) of disubstituted anhydrides has been shown to be possible for the first time. Using an ad hoc designed organocatalyst and an enantio- and diastereoselective cycloaddition process with aldehydes, stereochemically complex γ-butyrolactone derivatives can be obtained-with control over three contiguous stereocentres, one of which is all carbon quaternary.

CONVENIENT METHOD FOR THE PREPARATION OF LITHIUM

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