Cas 1254206-92-2,tert-butyl (S)-2-(benzyloxy)-1-((S)-5,5-dimethyl-2,5-dihydrofuran-2-yl)ethylcarbamate

1254206-92-2

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Basic information

Product Name: tert-butyl (S)-2-(benzyloxy)-1-((S)-5,5-dimethyl-2,5-dihydrofuran-2-yl)ethylcarbamate
Synonyms: tert-butyl (S)-2-(benzyloxy)-1-((S)-5,5-dimethyl-2,5-dihydrofuran-2-yl)ethylcarbamate
CAS NO:1254206-92-2
Molecular Formula:
Molecular Weight: 347.455
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 (S)-2-(benzyloxy)-1-((S)-5,5-dimethyl-2,5-dihydrofuran-2-yl)ethylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (S)-2-(benzyloxy)-1-((S)-5,5-dimethyl-2,5-dihydrofuran-2-yl)ethylcarbamate(1254206-92-2)
EPA Substance Registry System: tert-butyl (S)-2-(benzyloxy)-1-((S)-5,5-dimethyl-2,5-dihydrofuran-2-yl)ethylcarbamate(1254206-92-2)

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: 1254206-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1254206-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,2,0 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1254206-92:
(9*1)+(8*2)+(7*5)+(6*4)+(5*2)+(4*0)+(3*6)+(2*9)+(1*2)=132
132 % 10 = 2
So 1254206-92-2 is a valid CAS Registry Number.

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1254206-92-2Relevant academic research and scientific papers

Metalated aziridines for cross-coupling with aryl and alkenyl halides via palladium catalysis

Nelson, John M.,Vedejs, Edwin

supporting information; experimental part, p. 5085 - 5087 (2011/01/05)

The palladium-catalyzed coupling of an aziridinylzinc chloride intermediate with alkenyl and aryl halides has been demonstrated. The method provides products with retention of aziridine stereochemistry. The utility of the coupling procedure is illustrated

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