Cas 955137-24-3,2-[{1-n-butyl-4-(o-nitrophenoxy)pyrimidin-2-one-5-yl}-1',3'-dithiol-2'-ylidene]-1,3-dithiole

955137-24-3

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Basic information

Product Name: 2-[{1-n-butyl-4-(o-nitrophenoxy)pyrimidin-2-one-5-yl}-1',3'-dithiol-2'-ylidene]-1,3-dithiole
Synonyms:
CAS NO:955137-24-3
Molecular Formula:
Molecular Weight: 491.637
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-[{1-n-butyl-4-(o-nitrophenoxy)pyrimidin-2-one-5-yl}-1',3'-dithiol-2'-ylidene]-1,3-dithiole(CAS DataBase Reference)
NIST Chemistry Reference: 2-[{1-n-butyl-4-(o-nitrophenoxy)pyrimidin-2-one-5-yl}-1',3'-dithiol-2'-ylidene]-1,3-dithiole(955137-24-3)
EPA Substance Registry System: 2-[{1-n-butyl-4-(o-nitrophenoxy)pyrimidin-2-one-5-yl}-1',3'-dithiol-2'-ylidene]-1,3-dithiole(955137-24-3)

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: 955137-24-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 955137-24-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,5,1,3 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 955137-24:
(8*9)+(7*5)+(6*5)+(5*1)+(4*3)+(3*7)+(2*2)+(1*4)=183
183 % 10 = 3
So 955137-24-3 is a valid CAS Registry Number.

955137-24-3Upstream product

139698-09-2 (n-buthylstannyl)tetrathiafulvalene

955137-24-3Downstream Products

955137-24-3Relevant academic research and scientific papers

TTF-cytosine dyad as an electron-donor molecule having proton-accepting ability: Formation of hemiprotonated cytosine Dimer in i3- salt

Miyazaki, Eigo,Morita, Yasushi,Yakiyama, Yumi,Maki, Suguru,Umemoto, Yoshikazu,Ohmoto, Makoto,Nakasuji, Kazuhiro

, p. 1102 - 1103 (2007)

A tetrathiafulvalene (TTF) derivative with a cytosine moiety was designed and synthesized as a bi-functional molecule with both electron-donating and proton-accepting abilities. In the crystal of I3- salt, TTF-cytosine dyad formed a

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