Cas 449144-84-7,thioacetic acid <i>S</i>-{4-[5''-(4-acetylsulfanyl-phenylethynyl)-[2,2';6',2'']terpyridin-5-ylethynyl]-phenyl} ester

449144-84-7

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Basic information

Product Name: thioacetic acid S-{4-[5''-(4-acetylsulfanyl-phenylethynyl)-[2,2';6',2'']terpyridin-5-ylethynyl]-phenyl} ester
Synonyms:
CAS NO:449144-84-7
Molecular Formula:
Molecular Weight: 581.719
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: thioacetic acid S-{4-[5''-(4-acetylsulfanyl-phenylethynyl)-[2,2';6',2'']terpyridin-5-ylethynyl]-phenyl} ester(CAS DataBase Reference)
NIST Chemistry Reference: thioacetic acid S-{4-[5''-(4-acetylsulfanyl-phenylethynyl)-[2,2';6',2'']terpyridin-5-ylethynyl]-phenyl} ester(449144-84-7)
EPA Substance Registry System: thioacetic acid S-{4-[5''-(4-acetylsulfanyl-phenylethynyl)-[2,2';6',2'']terpyridin-5-ylethynyl]-phenyl} ester(449144-84-7)

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: 449144-84-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 449144-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,9,1,4 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 449144-84:
(8*4)+(7*4)+(6*9)+(5*1)+(4*4)+(3*4)+(2*8)+(1*4)=167
167 % 10 = 7
So 449144-84-7 is a valid CAS Registry Number.

449144-84-7Upstream product

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449144-84-7Relevant academic research and scientific papers

Ruthenium complexes containing fully conjugated ligands terminated with thiol groups

Otsuki, Joe,Kameda, Hiroyuki,Tomihira, Sota,Sakaguchi, Hiroshi,Takido, Toshio

, p. 610 - 611 (2007/10/03)

Bipyridine- and terpyridine-based ruthenium complexes containing fully conjugated ligands terminated with thiol groups were prepared and immobilized in self-assembled monolayers of alkanethiolates on gold surface, single molecules of which were observed w

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