38873-94-8

Basic information

• Product Name: Phosphonic acid, ethyl-, bis(4-nitrophenyl) ester
• Synonyms: Aethyl-phosphonsaeure-bis-(4-nitro-phenylester);ethyl-phosphonic acid bis-(4-nitro-phenyl ester);Phosphonic acid,ethyl-,bis(4-nitrophenyl) ester;ethylphosphonic acid bis(nitrophenyl)ester
• CAS NO: 38873-94-8
• Molecular Formula: C14H13N2O7P
• Molecular Weight: 352.24
• Mol File: 38873-94-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 138 °C
• Boiling Point: 512.0±50.0 °C(Predicted)
• Density: 1.430±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Phosphonic acid, ethyl-, bis(4-nitrophenyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, ethyl-, bis(4-nitrophenyl) ester(38873-94-8)
• EPA Substance Registry System: Phosphonic acid, ethyl-, bis(4-nitrophenyl) ester(38873-94-8)

Safety Data

• Hazardous Substances Data: 38873-94-8(Hazardous Substances Data)

Upstream product

• 100-02-7 4-nitro-phenol 
• 1066-50-8 Ethylphosphonic dichloride 

Downstream Products

• 71002-67-0 butyl p-nitrophenyl ethylphosphonate 
• 1428268-02-3 2-fluoroethyl 4-nitrophenyl ethylphosphonate 
• 368874-04-8 C₈H₁₀NO₅P 
• 1428268-19-2 C₁₁H₁₅BrNO₄PS 
• 4230-68-6 C₁₀H₁₃BrNO₄PS 
• 1428268-18-1 C₁₁H₁₅INO₄PS 
• 1428268-17-0 C₁₀H₁₃INO₄PS 
• 1428268-14-7 C₁₀H₁₃FNO₄PS 
• 1428268-13-6 C₁₁H₁₅BrNO₅P 
• 1428268-12-5 2-bromoethyl 4-nitrophenyl ethylphosphonate 
• 1428268-11-4 C₁₁H₁₅INO₅P 
• 1428268-10-3 2-iodoethyl 4-nitrophenyl ethylphosphonate 

Relevant articles and documents

Balancing Specificity and Promiscuity in Enzyme Evolution: Multidimensional Activity Transitions in the Alkaline Phosphatase Superfamily

Highly proficient, promiscuous enzymes can be springboards for functional evolution, able to avoid loss of function during adaptation by their capacity to promote multiple reactions. We employ a systematic comparative study of structure, sequence, and sub

Synthesis and anti-acetylcholinesterase properties of novel β- And γ-substituted alkoxy organophosphonates

Activated organophosphate (OP) insecticides and chemical agents inhibit acetylcholinesterase (AChE) to form OP-AChE adducts. Whereas the structure of the OP correlates with the rate of inhibition, the structure of the OP-AChE adduct influences the rate at