Cas 497155-65-4,[cyclohexylmeth-(Z)-ylidene][(3aS,4S,6R,6aS)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]amine N-oxide

497155-65-4

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Product Name: [cyclohexylmeth-(Z)-ylidene][(3aS,4S,6R,6aS)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]amine N-oxide
Synonyms: [cyclohexylmeth-(Z)-ylidene][(3aS,4S,6R,6aS)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]amine N-oxide
CAS NO:497155-65-4
Molecular Formula:
Molecular Weight: 369.458
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: [cyclohexylmeth-(Z)-ylidene][(3aS,4S,6R,6aS)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]amine N-oxide(CAS DataBase Reference)
NIST Chemistry Reference: [cyclohexylmeth-(Z)-ylidene][(3aS,4S,6R,6aS)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]amine N-oxide(497155-65-4)
EPA Substance Registry System: [cyclohexylmeth-(Z)-ylidene][(3aS,4S,6R,6aS)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]amine N-oxide(497155-65-4)

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: 497155-65-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 497155-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,1,5 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 497155-65:
(8*4)+(7*9)+(6*7)+(5*1)+(4*5)+(3*5)+(2*6)+(1*5)=194
194 % 10 = 4
So 497155-65-4 is a valid CAS Registry Number.

497155-65-4Upstream product

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497155-65-4Relevant academic research and scientific papers

ZnCl2-mediated stereoselective addition of terminal alkynes to D-(+)-mannofuranosyl nitrones

Topic, Dana,Aschwanden, Patrick,Faessler, Roger,Carreira, Erick M.

, p. 5329 - 5330 (2007/10/03)

(Chemical Equation Presented) An optimized process for the addition of terminal alkynes to chiral nitrones using ZnCl2 and NEt3 in toluene is reported. The new reaction protocol is facile to perform and cost-effective. The resulting

1,2,4-Oxadiazolidinones as configurationally stable chiral building blocks

Ritter, Tobias,Carreira, Erick M.

, p. 936 - 938 (2007/10/03)

An intriguing scaffold for drug development, 1,2,4-oxadiazolidinones are obtained in enantiomerically pure form by a simple reaction and purification protocol (see scheme). These heterocycles, including the previously unknown N2-unsubstituted parent struc

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