Cas 13696-02-1,p-(1-Methyl-4-<1-methyl-4-(1-methyl-4-nitropyrryl-(2)-carbonylamino)-pyrryl-(2)-carbonylamino>-pyrryl-(2)-carbonylamino)-benzonitril

13696-02-1

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Basic information

Product Name: p-(1-Methyl-4-<1-methyl-4-(1-methyl-4-nitropyrryl-(2)-carbonylamino)-pyrryl-(2)-carbonylamino>-pyrryl-(2)-carbonylamino)-benzonitril
Synonyms:
CAS NO:13696-02-1
Molecular Formula:
Molecular Weight: 514.5
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: p-(1-Methyl-4-<1-methyl-4-(1-methyl-4-nitropyrryl-(2)-carbonylamino)-pyrryl-(2)-carbonylamino>-pyrryl-(2)-carbonylamino)-benzonitril(CAS DataBase Reference)
NIST Chemistry Reference: p-(1-Methyl-4-<1-methyl-4-(1-methyl-4-nitropyrryl-(2)-carbonylamino)-pyrryl-(2)-carbonylamino>-pyrryl-(2)-carbonylamino)-benzonitril(13696-02-1)
EPA Substance Registry System: p-(1-Methyl-4-<1-methyl-4-(1-methyl-4-nitropyrryl-(2)-carbonylamino)-pyrryl-(2)-carbonylamino>-pyrryl-(2)-carbonylamino)-benzonitril(13696-02-1)

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: 13696-02-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 13696-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,9 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13696-02:
(7*1)+(6*3)+(5*6)+(4*9)+(3*6)+(2*0)+(1*2)=111
111 % 10 = 1
So 13696-02-1 is a valid CAS Registry Number.

13696-02-1Upstream product

13696-02-1Downstream Products

13696-02-1Relevant academic research and scientific papers

Structure--activity relationships of pyrrole amidine antiviral antibiotics. 1. Modifications of the alkylamidine side chain.

Bialer et al.

, p. 1296,1299 (1979)

Representatives of three types of side-chain analogues of distamycin A (1) were synthesized. These were tested for cytotoxicity, inhibition of herpes simplex virus (HSV) replication in cultured cells, effects on the synthesis of HSV DNA in isolated nuclei in vitro, as well as on DNA synthesis by purified HSV DNA polymerase. Distamycin A was the most active compound in all three antiviral tests, as well as the most toxic. However, several compounds, in particular the aromatic analogues 15 and 16, showed no toxicity under the experimental conditions used but were still very active in the three antiviral tests.

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