Cas 1243210-34-5,ethyl 2-(4-methoxybenzyloxy)-4-(5-oxo-1,2,3,5-tetrahydroindolizin-6-yloxy)but-2-enoate

1243210-34-5

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Basic information

Product Name: ethyl 2-(4-methoxybenzyloxy)-4-(5-oxo-1,2,3,5-tetrahydroindolizin-6-yloxy)but-2-enoate
Synonyms: ethyl 2-(4-methoxybenzyloxy)-4-(5-oxo-1,2,3,5-tetrahydroindolizin-6-yloxy)but-2-enoate
CAS NO:1243210-34-5
Molecular Formula:
Molecular Weight: 399.444
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: ethyl 2-(4-methoxybenzyloxy)-4-(5-oxo-1,2,3,5-tetrahydroindolizin-6-yloxy)but-2-enoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-(4-methoxybenzyloxy)-4-(5-oxo-1,2,3,5-tetrahydroindolizin-6-yloxy)but-2-enoate(1243210-34-5)
EPA Substance Registry System: ethyl 2-(4-methoxybenzyloxy)-4-(5-oxo-1,2,3,5-tetrahydroindolizin-6-yloxy)but-2-enoate(1243210-34-5)

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: 1243210-34-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1243210-34-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,3,2,1 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1243210-34:
(9*1)+(8*2)+(7*4)+(6*3)+(5*2)+(4*1)+(3*0)+(2*3)+(1*4)=95
95 % 10 = 5
So 1243210-34-5 is a valid CAS Registry Number.

1243210-34-5Upstream product

1243210-34-5Downstream Products

1243210-34-5Relevant academic research and scientific papers

Total synthesis of (±)-17-norcamptothecin, a novel E-ring modified camptothecin

Devert, Marie,Sabot, Cyrille,Giboreau, Pascale,Constant, Jean-Franois,Greene, Andrew E.,Kanazawa, Alice

experimental part, p. 7227 - 7231 (2010/09/30)

The first total synthesis of (±)-17-norcamptothecin, a novel camptothecin analog possessing an α-hydroxy-γ-lactone E-ring, has been accomplished by using a short and flexible route. The stability of this new compound in aqueous medium has been evaluated t

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