Cas 299409-53-3,(Z)-N-{[(4S,5R)-3-(tert-butoxycarbonyl)-2,2,5-trimethyl-1,3-oxazolidin-4-yl]methylidene}benzylamine N-oxide

299409-53-3

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Basic information

Product Name: (Z)-N-{[(4S,5R)-3-(tert-butoxycarbonyl)-2,2,5-trimethyl-1,3-oxazolidin-4-yl]methylidene}benzylamine N-oxide
Synonyms: (Z)-N-{[(4S,5R)-3-(tert-butoxycarbonyl)-2,2,5-trimethyl-1,3-oxazolidin-4-yl]methylidene}benzylamine N-oxide
CAS NO:299409-53-3
Molecular Formula:
Molecular Weight: 348.442
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: (Z)-N-{[(4S,5R)-3-(tert-butoxycarbonyl)-2,2,5-trimethyl-1,3-oxazolidin-4-yl]methylidene}benzylamine N-oxide(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-N-{[(4S,5R)-3-(tert-butoxycarbonyl)-2,2,5-trimethyl-1,3-oxazolidin-4-yl]methylidene}benzylamine N-oxide(299409-53-3)
EPA Substance Registry System: (Z)-N-{[(4S,5R)-3-(tert-butoxycarbonyl)-2,2,5-trimethyl-1,3-oxazolidin-4-yl]methylidene}benzylamine N-oxide(299409-53-3)

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: 299409-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 299409-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,4,0 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 299409-53:
(8*2)+(7*9)+(6*9)+(5*4)+(4*0)+(3*9)+(2*5)+(1*3)=193
193 % 10 = 3
So 299409-53-3 is a valid CAS Registry Number.

299409-53-3Upstream product

299409-53-3Downstream Products

299409-54-4 (3S,4R,5R)-3-(N-benzylhydroxylamino)-4-(tert-butoxycarbonylamino)-5-hydroxy-4,5-O-isopropylidene-1-hexene

299409-53-3Relevant academic research and scientific papers

A new and expedient diastereoselective synthesis of α-(hydroxyamino)phosphonates and α-aminophosphonates by silyl trifiate promoted diethyl phosphite addition to chiral N-benzyl nitrones

De Risi, Carmela,Perrone, Daniela,Dondoni, Alessandro,Pollini, Gian Piero,Bertolasi, Valerio

, p. 1904 - 1914 (2007/10/03)

An efficient methodology for the synthesis of α-aminophosphonates has been developed taking advantage of the tertbutyldimethylsilyl triflate activated addition of diethyl phosphite to N-benzyl nitrones derived from chiral α-alkoxy and α-(Boc-amino) aldehy

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