10550-79-5

Basic information

• Product Name: 1,1,2,2-Propanetetracarbonxamide
• Synonyms: 1,1,2,2-Propanetetracarbonxamide
• CAS NO: 10550-79-5
• Molecular Formula: C7H12 N4 O4
• Molecular Weight: 216.19
• Mol File: 10550-79-5.mol
• Article Data: 6

Chemical Properties

• Melting Point: 257 °C (decomp)
• Boiling Point: 779.3°Cat760mmHg
• Flash Point: 425.1°C
• Appearance: /
• Density: 1.46g/cm³
• Vapor Pressure: 3.16E-24mmHg at 25°C
• Refractive Index: 1.571
• PKA: 6.21±0.70(Predicted)
• CAS DataBase Reference: 1,1,2,2-Propanetetracarbonxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,2,2-Propanetetracarbonxamide(10550-79-5)
• EPA Substance Registry System: 1,1,2,2-Propanetetracarbonxamide(10550-79-5)

Safety Data

• Hazardous Substances Data: 10550-79-5(Hazardous Substances Data)

Usage

General Description

1,1,2,2-Propanetetracarboxamide is a chemical compound with the molecular formula C7H12N4O4. It is a derivative of propanetetracarboxylic acid and is used as a crosslinking agent in the production of polymers and resins. It is also utilized as a curing agent for epoxy resins, and as a flame retardant in plastics. With its ability to form strong and stable bonds between polymer chains, 1,1,2,2-Propanetetracarboxamide plays a crucial role in improving the mechanical and thermal properties of various materials. Additionally, it is known for its low toxicity and environmental compatibility, making it a popular choice in the chemical and manufacturing industries.

InChI:InChI=1/C7H12N4O4/c8-4(12)2(5(9)13)1-3(6(10)14)7(11)15/h2-3H,1H2,(H2,8,12)(H2,9,13)(H2,10,14)(H2,11,15)

Upstream product

• 2121-66-6 tetraethyl 1,1,3,3-propanetetracarboxylate 
• 880-09-1 di(N-piperidinyl)methane 
• 108-13-4 malonodiamide 
• 50-00-0 formaldehyd 
• 75-09-2 dichloromethane 
• 28781-92-2 Propane-1,1,3,3-tetracarboxylic acid tetramethyl ester 
• 563-83-7 ISOPROPYLAMIDE 

Downstream Products

• 4889-98-9 2,4,6,8-tetraoxo-3,7-diazabicyclo[3.3.1]nonane 
• 1415208-73-9 1,1,3,3-Tetra(salicylideneiminomethyl)propane 

Relevant articles and documents

A practical synthesis of (±)-α-isosparteine from a tetraoxobispidine core

(Chemical Equation Presented) The title alkaloid was synthesized in racemic form from 3,7-diallyl-2,4,6,8-tetraoxo-3,7-diazabicyclo[3.3.1]nonane (7) by a regioselective diallylation reaction followed by double ring-closing olefin metathesis and exhaustive reduction. Tetraoxobispidine 7 was itself prepared in three simple operations from dimethyl malonate. The entire sequence to α-isosparteine was conducted on a multigram scale and proceeded without recourse to chromatography.

Synthesis and characterization of binuclear Co(II) complexes with bis(salen-type) ligands

Two new, bridged bis(salen-type) ligand precursors, 1,1,3,3- tetrakis(salicylidene-3-iminopropyl)butylenediamine (I) and 1,1,3,3- tetra(salicylideneiminomethyl)propane (IV), were prepared by Schiff base condensation of salicylaldehyde with appropriate tet

Synthesis, Physicochemical and Pharmacological Properties of N,N′,N″, N?-Substituted Amides of 1,1,3,3- Propanetetracarboxylic Acid

By condensation of symmetrical malonic acid diamides with dichloromethane (method a) and with paraform (method b) N,N′,N″,N?- substituted amides of 1,1,3,3-propanetetracarboxylic acid were synthesized. Better yields of the target products (68-80%) and the use of less toxic reagents indicate that method b is more feasible. The primary pharmacological screening revealed that the compounds obtained possess pronounced anticonvulsant activity at moderate toxicity.