Cas 851957-93-2,N-acetyl-3,5-bis((p-dimethylaminophenyl)thiomethyl)phenylpalladium trifluoroacetate

851957-93-2

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Basic information

Product Name: N-acetyl-3,5-bis((p-dimethylaminophenyl)thiomethyl)phenylpalladium trifluoroacetate
Synonyms:
CAS NO:851957-93-2
Molecular Formula:
Molecular Weight: 684.112
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: N-acetyl-3,5-bis((p-dimethylaminophenyl)thiomethyl)phenylpalladium trifluoroacetate(CAS DataBase Reference)
NIST Chemistry Reference: N-acetyl-3,5-bis((p-dimethylaminophenyl)thiomethyl)phenylpalladium trifluoroacetate(851957-93-2)
EPA Substance Registry System: N-acetyl-3,5-bis((p-dimethylaminophenyl)thiomethyl)phenylpalladium trifluoroacetate(851957-93-2)

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: 851957-93-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 851957-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,9,5 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 851957-93:
(8*8)+(7*5)+(6*1)+(5*9)+(4*5)+(3*7)+(2*9)+(1*3)=212
212 % 10 = 2
So 851957-93-2 is a valid CAS Registry Number.

851957-93-2Upstream product

851957-98-7 N-acetyl-3,5-bis((p-dimethylaminophenyl)thiomethyl)aniline

851957-93-2Downstream Products

851957-93-2Relevant academic research and scientific papers

Synthesis and characterization of electronically varied XCX palladacycles with functional arene groups

Bergbreiter, David E.,Frels, Jonathon D.,Rawson, Jeffrey,Li, Jun,Reibenspies, Joseph H.

, p. 1912 - 1922 (2008/10/09)

X-ray crystallographic studies show that varying the nature of the S-aryl ligands in SCS-Pd(II) pincer complexes and the electronic nature of the aryl substituent para to the Pd(II) group in PCP-Pd(II) pincer complexes do not lead to structural changes in

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