Cas 133765-82-9,2-<2-<3-<3-(guanidinoacetamido)benzene-1-carboxamido>benzene-1-carboxamido>ethyl>imidazoline

133765-82-9

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Basic information

Product Name: 2-<2-<3-<3-(guanidinoacetamido)benzene-1-carboxamido>benzene-1-carboxamido>ethyl>imidazoline
Synonyms:
CAS NO:133765-82-9
Molecular Formula:
Molecular Weight: 450.5
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: 2-<2-<3-<3-(guanidinoacetamido)benzene-1-carboxamido>benzene-1-carboxamido>ethyl>imidazoline(CAS DataBase Reference)
NIST Chemistry Reference: 2-<2-<3-<3-(guanidinoacetamido)benzene-1-carboxamido>benzene-1-carboxamido>ethyl>imidazoline(133765-82-9)
EPA Substance Registry System: 2-<2-<3-<3-(guanidinoacetamido)benzene-1-carboxamido>benzene-1-carboxamido>ethyl>imidazoline(133765-82-9)

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: 133765-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133765-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,7,6 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133765-82:
(8*1)+(7*3)+(6*3)+(5*7)+(4*6)+(3*5)+(2*8)+(1*2)=139
139 % 10 = 9
So 133765-82-9 is a valid CAS Registry Number.

133765-82-9Upstream product

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133765-82-9Relevant academic research and scientific papers

Synthesis, DNA binding properties and biological evaluation of novel oligo-meta-benzamides related to netropsin

Debart,Gosselin,Rayner,Le Ber,Auclair,Balzarini,De Clercq,Paoletti,Imbach

, p. 261 - 271 (2007/10/02)

A series of oligo-meta-benzamides structurally related to the natural agent netropsin have been synthesized. Their binding constants to double-stranded polynucleotides as well as their cytostatic activity against tumor cell lines and their in vitro activi

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