608-82-2

Basic information

• Product Name: diethyl 2,3-dibromobutanedioate
• Synonyms: butanedioic acid, 2,3-dibromo-, diethyl ester; Diethyl 2,3-dibromosuccinate
• CAS NO: 608-82-2
• Molecular Formula: C₈H₁₂Br₂O₄
• Molecular Weight: 331.9865
• Mol File: 608-82-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 290.9°C at 760 mmHg
• Flash Point: 129.7°C
• Density: 1.705g/cm³
• Vapor Pressure: 0.00201mmHg at 25°C
• Refractive Index: 1.508
• CAS DataBase Reference: diethyl 2,3-dibromobutanedioate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl 2,3-dibromobutanedioate(608-82-2)
• EPA Substance Registry System: diethyl 2,3-dibromobutanedioate(608-82-2)

Safety Data

• Hazardous Substances Data: 608-82-2(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 7726-95-6 bromine 
• 623-91-6 diethyl Fumarate 
• 141-05-9 Diethyl maleate 
• 87-91-2 diethyl (2R,3R)-tartrate 
• 1114-31-4 diethyl meso-2,3-dibromosuccinate 
• 1520-50-9 but-2-enedioic acid diethyl ester 

Downstream Products

• 698976-26-0 3-carbamoyl-aziridine-2-carboxylic acid ethyl ester 
• 623-91-6 diethyl Fumarate 
• 10035-10-6 hydrogen bromide 
• 141-05-9 Diethyl maleate 
• 861520-44-7 4-oxo-4-phenyl-butane-1,2,3-tricarboxylic acid triethyl ester 
• 1092776-44-7 3-bromo-1,2-dimethylindazolium bromide 
• 880142-59-6 diethyl (Z)-2-(4-chlorophenoxy)-2-butenedioate 
• 1187-16-2 4-oxo-pentane-1,2,3-tricarboxylic acid triethyl ester 
• 2049-86-7 Diethyl 2,3-diacetylsuccinate 
• 632-56-4 tetraethyl ethane-1,1,2,2-tetracarboxylate 

Relevant articles and documents

Understanding the binding properties of phosphorylated glycoluril-derived molecular tweezers and selective nanomolar binding of natural polyamines in aqueous solution

A modular synthetic platform for the construction of flexible glycoluril-derived molecular tweezers was developed. The binding properties of four exemplary supramolecular hosts obtained via this approach towards 16 organic amines were investigated by means of 1H NMR titration. In this work, we compare the Ka values obtained this way with those of three structurally related molecular tweezers and provide a computational approach towards an explanation of the observed behavior of those novel hosts. The results showcase that certain structural modifications lead to very potent and selective binders of natural polyamines, with observed binding of spermine below 10 nM. This journal is

Tetrameric DABCO-bromine: An efficient and versatile reagent for bromination of various organic compounds

Tetrameric DABCO-bromine is a powerful brominating agent but shows reasonable selectivity with certain substrates. The selective bromination for activated aromatic compounds and alkenes is reported. Synthesis of α-bromo ketones and nitriles has also been achieved by using this reagent and the results are also reported. All products reported were obtained in good to excellent yields.