Cas 450409-33-3,(E)-3-(3,4-Bis-benzyloxy-phenyl)-N-[3-(6-{3-[(E)-3-(3,4-bis-benzyloxy-phenyl)-acryloylamino]-propyl}-[1,6]diazecan-1-yl)-propyl]-acrylamide

450409-33-3

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Basic information

Product Name: (E)-3-(3,4-Bis-benzyloxy-phenyl)-N-[3-(6-{3-[(E)-3-(3,4-bis-benzyloxy-phenyl)-acryloylamino]-propyl}-[1,6]diazecan-1-yl)-propyl]-acrylamide
Synonyms: (E)-3-(3,4-Bis-benzyloxy-phenyl)-N-[3-(6-{3-[(E)-3-(3,4-bis-benzyloxy-phenyl)-acryloylamino]-propyl}-[1,6]diazecan-1-yl)-propyl]-acrylamide
CAS NO:450409-33-3
Molecular Formula:
Molecular Weight: 941.223
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: (E)-3-(3,4-Bis-benzyloxy-phenyl)-N-[3-(6-{3-[(E)-3-(3,4-bis-benzyloxy-phenyl)-acryloylamino]-propyl}-[1,6]diazecan-1-yl)-propyl]-acrylamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(3,4-Bis-benzyloxy-phenyl)-N-[3-(6-{3-[(E)-3-(3,4-bis-benzyloxy-phenyl)-acryloylamino]-propyl}-[1,6]diazecan-1-yl)-propyl]-acrylamide(450409-33-3)
EPA Substance Registry System: (E)-3-(3,4-Bis-benzyloxy-phenyl)-N-[3-(6-{3-[(E)-3-(3,4-bis-benzyloxy-phenyl)-acryloylamino]-propyl}-[1,6]diazecan-1-yl)-propyl]-acrylamide(450409-33-3)

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: 450409-33-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 450409-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,0,4,0 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 450409-33:
(8*4)+(7*5)+(6*0)+(5*4)+(4*0)+(3*9)+(2*3)+(1*3)=123
123 % 10 = 3
So 450409-33-3 is a valid CAS Registry Number.

450409-33-3Upstream product

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450409-33-3Relevant academic research and scientific papers

Simple syntheses of cyclic polyamines using selectively N-tritylated polyamines and succinic anhydride

Militsopoulou, Maria,Tsiakopoulos, Nikolaos,Chochos, Christos,Magoulas, George,Papaioannou, Dionissios

, p. 2593 - 2596 (2007/10/03)

Treatment of selectively N-tritylated spermidine and spermine derivatives with succinic anhydride, followed by PyBrOP-mediated intramolecular amide bond formation and LiAlH4 reduction, allows for an easy and general entry to cyclic polyamine derivatives.

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