Cas 53678-50-5,Phosphonic acid, [1-hydroxy-1-(nitromethyl)-2-phenylethyl]-, bis(1-methylethyl) ester

53678-50-5

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Basic information

Product Name: Phosphonic acid, [1-hydroxy-1-(nitromethyl)-2-phenylethyl]-, bis(1-methylethyl) ester
Synonyms:
CAS NO:53678-50-5
Molecular Formula: C15H24NO6P
Molecular Weight: 345.332
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Phosphonic acid, [1-hydroxy-1-(nitromethyl)-2-phenylethyl]-, bis(1-methylethyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: Phosphonic acid, [1-hydroxy-1-(nitromethyl)-2-phenylethyl]-, bis(1-methylethyl) ester(53678-50-5)
EPA Substance Registry System: Phosphonic acid, [1-hydroxy-1-(nitromethyl)-2-phenylethyl]-, bis(1-methylethyl) ester(53678-50-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 53678-50-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 53678-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,7 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53678-50:
(7*5)+(6*3)+(5*6)+(4*7)+(3*8)+(2*5)+(1*0)=145
145 % 10 = 5
So 53678-50-5 is a valid CAS Registry Number.

53678-50-5Upstream product

53678-50-5Downstream Products

57915-30-7 (1-Aminomethyl-1-hydroxy-2-phenyl-ethyl)-phosphonic acid

53678-50-5Relevant academic research and scientific papers

Studies on organophosphorus compounds, 53: A new procedure for the synthesis of 1-alkyl or 1-aryl-1-hydroxy-2-nitroethylphosphonates under PTC conditions

Yuan,Cui,Wang,Feng,Chen,Li,Ding,Maier

, p. 258 - 260 (1992)

A series of dialkyl 1-alkyl- or 1-aryl-1-hydroxy-2-nitroethyl-phosphonates and 1-hydroxy-1-(nitromethyl)alkylphosphonates was prepared by nucleophilic addition of nitromethane to dialkyl acylphosphonates in the presence of potassium carbonate and tetrabutylammonium bromide.

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