Cas 1423779-06-9,tert-butyl N-{(2S)-1-[(2S)-2-({1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamoyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate

1423779-06-9

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Basic information

Product Name: tert-butyl N-{(2S)-1-[(2S)-2-({1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamoyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
Synonyms: tert-butyl N-{(2S)-1-[(2S)-2-({1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamoyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate
CAS NO:1423779-06-9
Molecular Formula:
Molecular Weight: 661.579
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: tert-butyl N-{(2S)-1-[(2S)-2-({1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamoyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl N-{(2S)-1-[(2S)-2-({1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamoyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate(1423779-06-9)
EPA Substance Registry System: tert-butyl N-{(2S)-1-[(2S)-2-({1-[bis(2,2,2-trifluoroethoxy)phosphoryl]-2-phenylethyl}carbamoyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}carbamate(1423779-06-9)

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: 1423779-06-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1423779-06-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,7,7 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1423779-06:
(9*1)+(8*4)+(7*2)+(6*3)+(5*7)+(4*7)+(3*9)+(2*0)+(1*6)=169
169 % 10 = 9
So 1423779-06-9 is a valid CAS Registry Number.

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1423779-06-9Relevant academic research and scientific papers

Efficient methods for the synthesis of α-aminophosphonate fluoroalkyl esters

Skoreński, Marcin,Oleksyszyn, Józef,Sieńczyk, Marcin

supporting information, p. 1566 - 1568 (2013/03/28)

Two novel synthetic methods for the preparation of bis(trifluoroethyl) esters of α-aminophosphonic acids are presented. Preliminary results on the application of the compounds synthesized as inhibitors of serine proteases are also reported. Structures originating from α-aminoalkylphosphonate diaryl esters represent a novel class of serine protease inactivators.

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