Cas 1114265-48-3,Z-(2R,4aR,6S,10bS)-4,4a,6,10b-tetrahydro-6-methoxy-2-phenyl-9-(2-furyl)-1,3-dioxino[4',5':5,6]-pyrano[4,3-d]-pyrimidine

1114265-48-3

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Basic information

Product Name: Z-(2R,4aR,6S,10bS)-4,4a,6,10b-tetrahydro-6-methoxy-2-phenyl-9-(2-furyl)-1,3-dioxino[4',5':5,6]-pyrano[4,3-d]-pyrimidine
Synonyms: Z-(2R,4aR,6S,10bS)-4,4a,6,10b-tetrahydro-6-methoxy-2-phenyl-9-(2-furyl)-1,3-dioxino[4',5':5,6]-pyrano[4,3-d]-pyrimidine
CAS NO:1114265-48-3
Molecular Formula:
Molecular Weight: 366.373
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-(2R,4aR,6S,10bS)-4,4a,6,10b-tetrahydro-6-methoxy-2-phenyl-9-(2-furyl)-1,3-dioxino[4',5':5,6]-pyrano[4,3-d]-pyrimidine(CAS DataBase Reference)
NIST Chemistry Reference: Z-(2R,4aR,6S,10bS)-4,4a,6,10b-tetrahydro-6-methoxy-2-phenyl-9-(2-furyl)-1,3-dioxino[4',5':5,6]-pyrano[4,3-d]-pyrimidine(1114265-48-3)
EPA Substance Registry System: Z-(2R,4aR,6S,10bS)-4,4a,6,10b-tetrahydro-6-methoxy-2-phenyl-9-(2-furyl)-1,3-dioxino[4',5':5,6]-pyrano[4,3-d]-pyrimidine(1114265-48-3)

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: 1114265-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1114265-48-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,4,2,6 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1114265-48:
(9*1)+(8*1)+(7*1)+(6*4)+(5*2)+(4*6)+(3*5)+(2*4)+(1*8)=113
113 % 10 = 3
So 1114265-48-3 is a valid CAS Registry Number.

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1114265-48-3Relevant academic research and scientific papers

Efficient functionalizations of a pyranosido-pyrimidine scaffold

Samb, Issa,Pellegrini-Mo?se, Nadia,Lamandé-Langle, Sandrine,Chapleur, Yves

experimental part, p. 896 - 902 (2009/04/10)

Efficient reaction conditions have been developed to prepare highly functionalized chiral pyranosido-pyrimidine by regioselective alkylation of the pyranoside ring and palladium-catalyzed cross-coupling reaction on the pyrimidine ring under microwave acti

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