Cas 557792-67-3,Carbamic acid, [12-[[(2S)-3-[4-(1,1-dimethylethoxy)phenyl]-1-oxo-2-[(1-oxobutyl)amino] propyl]amino]dodecyl]-, 1,1-dimethylethyl ester

557792-67-3

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Basic information

Product Name: Carbamic acid, [12-[[(2S)-3-[4-(1,1-dimethylethoxy)phenyl]-1-oxo-2-[(1-oxobutyl)amino] propyl]amino]dodecyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:557792-67-3
Molecular Formula: C34H59N3O5
Molecular Weight: 589.86
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: Carbamic acid, [12-[[(2S)-3-[4-(1,1-dimethylethoxy)phenyl]-1-oxo-2-[(1-oxobutyl)amino] propyl]amino]dodecyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [12-[[(2S)-3-[4-(1,1-dimethylethoxy)phenyl]-1-oxo-2-[(1-oxobutyl)amino] propyl]amino]dodecyl]-, 1,1-dimethylethyl ester(557792-67-3)
EPA Substance Registry System: Carbamic acid, [12-[[(2S)-3-[4-(1,1-dimethylethoxy)phenyl]-1-oxo-2-[(1-oxobutyl)amino] propyl]amino]dodecyl]-, 1,1-dimethylethyl ester(557792-67-3)

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: 557792-67-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 557792-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,7,7,9 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 557792-67:
(8*5)+(7*5)+(6*7)+(5*7)+(4*9)+(3*2)+(2*6)+(1*7)=213
213 % 10 = 3
So 557792-67-3 is a valid CAS Registry Number.

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557792-67-3Relevant academic research and scientific papers

A sequential high-yielding large-scale solution-method for synthesis of philanthotoxin analogues

Wellendorph, Petrine,Jaroszewski, Jerzy W.,Hansen, Steen Honore,Franzyk, Henrik

, p. 117 - 122 (2007/10/03)

A general, improved procedure for rapid synthesis of philanthotoxin analogues, a pharmacologically important class of polyamine conjugates, is described. The solution-phase procedure is illustrated by gram-scale synthesis of philanthotoxins PhTX-343 and P

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