Cas 945483-85-2,2-[1-(diphenylphosphinoyl)-2-(hydroxyimino)propylamino]-3-methylbutyric acid ethyl ester

945483-85-2

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Basic information

Product Name: 2-[1-(diphenylphosphinoyl)-2-(hydroxyimino)propylamino]-3-methylbutyric acid ethyl ester
Synonyms: 2-[1-(diphenylphosphinoyl)-2-(hydroxyimino)propylamino]-3-methylbutyric acid ethyl ester
CAS NO:945483-85-2
Molecular Formula:
Molecular Weight: 416.457
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: 2-[1-(diphenylphosphinoyl)-2-(hydroxyimino)propylamino]-3-methylbutyric acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[1-(diphenylphosphinoyl)-2-(hydroxyimino)propylamino]-3-methylbutyric acid ethyl ester(945483-85-2)
EPA Substance Registry System: 2-[1-(diphenylphosphinoyl)-2-(hydroxyimino)propylamino]-3-methylbutyric acid ethyl ester(945483-85-2)

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: 945483-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 945483-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,4,8 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 945483-85:
(8*9)+(7*4)+(6*5)+(5*4)+(4*8)+(3*3)+(2*8)+(1*5)=212
212 % 10 = 2
So 945483-85-2 is a valid CAS Registry Number.

945483-85-2Upstream product

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945483-85-2Relevant academic research and scientific papers

Michael addition of amine derivatives to conjugate phosphinyl and phosphonyl nitrosoalkenes. Preparation of α-amino phosphine oxide and phosphonate derivatives

De Los Santos, Jesus M.,Ignacio, Roberto,Aparicio, Domitila,Palacios, Francisco

, p. 5202 - 5206 (2008/02/08)

(Chemical Equation Presented) The synthesis of nitrosoalkenes derived from phosphine oxides and phosphonates generated through base-mediated dehydrohalogenations of readily available α-halooximes is reported. These highly reactive intermediates act as Mic

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