Cas 244091-53-0,N-((1R)-1-methyl-2-oxo-2-phenylethyl)-N-[(tert-butoxy)carbonylamino](2,2,2-trichloroethoxy)carboxamide

244091-53-0

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Basic information

Product Name: N-((1R)-1-methyl-2-oxo-2-phenylethyl)-N-[(tert-butoxy)carbonylamino](2,2,2-trichloroethoxy)carboxamide
Synonyms: N-((1R)-1-methyl-2-oxo-2-phenylethyl)-N-[(tert-butoxy)carbonylamino](2,2,2-trichloroethoxy)carboxamide
CAS NO:244091-53-0
Molecular Formula:
Molecular Weight: 439.723
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: N-((1R)-1-methyl-2-oxo-2-phenylethyl)-N-[(tert-butoxy)carbonylamino](2,2,2-trichloroethoxy)carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((1R)-1-methyl-2-oxo-2-phenylethyl)-N-[(tert-butoxy)carbonylamino](2,2,2-trichloroethoxy)carboxamide(244091-53-0)
EPA Substance Registry System: N-((1R)-1-methyl-2-oxo-2-phenylethyl)-N-[(tert-butoxy)carbonylamino](2,2,2-trichloroethoxy)carboxamide(244091-53-0)

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: 244091-53-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 244091-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,0,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 244091-53:
(8*2)+(7*4)+(6*4)+(5*0)+(4*9)+(3*1)+(2*5)+(1*3)=120
120 % 10 = 0
So 244091-53-0 is a valid CAS Registry Number.

244091-53-0Upstream product

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244091-53-0Relevant academic research and scientific papers

Catalytic enantioselective amination of enolsilanes using C2-symmetric copper(II) complexes as chiral lewis acids

Evans, David A.,Johnson, Douglas S.

, p. 595 - 598 (2008/02/11)

(Matrix presented) [Cu(S,S)-t-Bu-box](OTf)2 (1) catalyzes the enantioselective amination of enolsilanes with azodicarboxylate derivatives. Isomerically pure enolsilanes of aryl ketones, acylpyrroles, and thioesters added to the azo-imide in gre

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