5467-28-7

Basic information

• Product Name: 1,1-di-tert-butyl 2,3-diethyl propane-1,1,2,3-tetracarboxylate
• CAS NO: 5467-28-7
• Molecular Formula: C₁₉H₃₂O₈
• Molecular Weight: 388.4526
• Mol File: 5467-28-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 430.7°C at 760 mmHg
• Flash Point: 182.5°C
• Density: 1.088g/cm³
• Vapor Pressure: 1.27E-07mmHg at 25°C
• Refractive Index: 1.455
• CAS DataBase Reference: 1,1-di-tert-butyl 2,3-diethyl propane-1,1,2,3-tetracarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-di-tert-butyl 2,3-diethyl propane-1,1,2,3-tetracarboxylate(5467-28-7)
• EPA Substance Registry System: 1,1-di-tert-butyl 2,3-diethyl propane-1,1,2,3-tetracarboxylate(5467-28-7)

Safety Data

• Hazardous Substances Data: 5467-28-7(Hazardous Substances Data)

Usage

Chemical structure

A complex structure with four carboxylate groups attached to a central carbon atom, which is bonded to two tert-butyl groups and two ethyl groups.

Derivative

It is a derivative of the widely used industrial solvent tetrachloroethylene.

Potential applications

It has potential applications in the fields of organic synthesis and materials science.

Unique structure

Its unique structure and properties make it an interesting target for further study and potential applications in various industries.

Carboxylate groups

The compound has four carboxylate groups, which are important for its chemical reactivity and potential applications.

Tert-butyl groups

The presence of two tert-butyl groups contributes to the compound's steric hindrance and stability.

Ethyl groups

The two ethyl groups attached to the central carbon atom provide additional functionality and potential for further chemical modification.

Industrial relevance

As a derivative of tetrachloroethylene, this compound may have potential applications in the industrial sector, particularly in the development of new materials and synthetic processes.

Further study

The compound's unique structure and potential applications warrant further research to better understand its properties and explore its use in various industries.

Upstream product

• 541-16-2 t-butyl malonate 
• 141-05-9 Diethyl maleate 

Relevant articles and documents

Lithium binaphtholate-catalyzed michael reaction of malonates with maleates and its application to the enantioselective synthesis of tricarboxylic acid derivatives

The Michael reaction of malonates with maleates afforded the corresponding adducts in high yields with high enantioselectivities (up to 98% enantiomeric excess (ee)) by using dilithium 3,3′-dichlorobinaphtholate as a catalyst. The obtained Michael adducts