Cas 353244-63-0,(3R,4R,5R)-4-Benzyloxy-5-((1S,2R,4R)-6,6-dimethyl-7-oxa-1-aza-bicyclo[2.2.1]hept-2-yl)-tetrahydro-furan-2,3-diol

353244-63-0

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Basic information

Product Name: (3R,4R,5R)-4-Benzyloxy-5-((1S,2R,4R)-6,6-dimethyl-7-oxa-1-aza-bicyclo[2.2.1]hept-2-yl)-tetrahydro-furan-2,3-diol
Synonyms: (3R,4R,5R)-4-Benzyloxy-5-((1S,2R,4R)-6,6-dimethyl-7-oxa-1-aza-bicyclo[2.2.1]hept-2-yl)-tetrahydro-furan-2,3-diol
CAS NO:353244-63-0
Molecular Formula:
Molecular Weight: 335.4
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: (3R,4R,5R)-4-Benzyloxy-5-((1S,2R,4R)-6,6-dimethyl-7-oxa-1-aza-bicyclo[2.2.1]hept-2-yl)-tetrahydro-furan-2,3-diol(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R,5R)-4-Benzyloxy-5-((1S,2R,4R)-6,6-dimethyl-7-oxa-1-aza-bicyclo[2.2.1]hept-2-yl)-tetrahydro-furan-2,3-diol(353244-63-0)
EPA Substance Registry System: (3R,4R,5R)-4-Benzyloxy-5-((1S,2R,4R)-6,6-dimethyl-7-oxa-1-aza-bicyclo[2.2.1]hept-2-yl)-tetrahydro-furan-2,3-diol(353244-63-0)

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: 353244-63-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 353244-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,4 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 353244-63:
(8*3)+(7*5)+(6*3)+(5*2)+(4*4)+(3*4)+(2*6)+(1*3)=130
130 % 10 = 0
So 353244-63-0 is a valid CAS Registry Number.

353244-63-0Upstream product

353244-63-0Downstream Products

1054663-69-2 Formic acid (1R,2S)-2-benzyloxy-1-((1S,2R,4R)-6,6-dimethyl-7-oxa-1-aza-bicyclo[2.2.1]hept-2-yl)-3-oxo-propyl ester

353244-63-0Relevant academic research and scientific papers

Asymmetric synthesis of novel polyhydroxylated derivatives of indolizidine and quinolizidine by intramolecular 1,3-dipolar cycloaddition of N-(3-alkenyl)nitrones

Gebarowski,Sas

, p. 915 - 916 (2007/10/03)

Reaction of 3.0-benzyl-1,2-O-isopropylidene-1,5-penta dialdo-α-D-xylofuranose with N-(1,1-dimethylbut-3-enyl)hydroxylamine followed by intramolecular 1,3-dipolar cycloaddition yields 7-oxa-1-azabicyclo[2.2.1]heptane derivative 4, which is easily converted

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