Cas 562099-98-3,2(3H)-Furanone, 3-[[(4S,6S)-5,6-dihydro-4-(4-methoxyphenyl)-2-phenyl-4H-1,3-oxazin-6- yl]oxy]dihydro-4,4-dimethyl-, (3R)-

562099-98-3

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Basic information

Product Name: 2(3H)-Furanone, 3-[[(4S,6S)-5,6-dihydro-4-(4-methoxyphenyl)-2-phenyl-4H-1,3-oxazin-6- yl]oxy]dihydro-4,4-dimethyl-, (3R)-
Synonyms:
CAS NO:562099-98-3
Molecular Formula: C23H25NO5
Molecular Weight: 395.455
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: 2(3H)-Furanone, 3-[[(4S,6S)-5,6-dihydro-4-(4-methoxyphenyl)-2-phenyl-4H-1,3-oxazin-6- yl]oxy]dihydro-4,4-dimethyl-, (3R)-(CAS DataBase Reference)
NIST Chemistry Reference: 2(3H)-Furanone, 3-[[(4S,6S)-5,6-dihydro-4-(4-methoxyphenyl)-2-phenyl-4H-1,3-oxazin-6- yl]oxy]dihydro-4,4-dimethyl-, (3R)-(562099-98-3)
EPA Substance Registry System: 2(3H)-Furanone, 3-[[(4S,6S)-5,6-dihydro-4-(4-methoxyphenyl)-2-phenyl-4H-1,3-oxazin-6- yl]oxy]dihydro-4,4-dimethyl-, (3R)-(562099-98-3)

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: 562099-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 562099-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,2,0,9 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 562099-98:
(8*5)+(7*6)+(6*2)+(5*0)+(4*9)+(3*9)+(2*9)+(1*8)=183
183 % 10 = 3
So 562099-98-3 is a valid CAS Registry Number.

562099-98-3Upstream product

562099-98-3Downstream Products

562100-15-6 (S)-N-[1-(4-methoxyphenyl)-2-formylethyl]benzamide

562099-98-3Relevant academic research and scientific papers

Novel use of N-benzoyl-N, O-acetals as N-acylimine equivalents in asymmetric heterocycloaddition: An extended enantioselective pathway to β-benzamido aldehydes

Gizecki, Patricia,Dhal, Robert,Poulard, Celine,Gosselin, Pascal,Dujardin, Gilles

, p. 4338 - 4344 (2007/10/03)

For the first time, easily available N-(α-methoxyalkyl)amides were successfully used as synthetic equivalents of N-acylimines in an asymmetric heterocycloaddition process. The facial-controlled formation of 6-alkoxydihydrooxazines was thus achieved by SnC

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