Cas 1201000-52-3,[(CH3NC5H3CHNC6H4OCH3)PdCl(NCCH3)](1+)*O3SCF3(1-)=[(CH3NC5H3CHNC6H4OCH3)PdCl(NCCH3)]O3SCF3

1201000-52-3

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Basic information

Product Name: [(CH₃NC₅H₃CHNC₆H₄OCH₃)PdCl(NCCH₃)]⁽¹⁺⁾*O₃SCF₃^(1-)=[(CH₃NC₅H₃CHNC₆H₄OCH₃)PdCl(NCCH₃)]O₃SCF₃
Synonyms:
CAS NO:1201000-52-3
Molecular Formula:
Molecular Weight: 558.274
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: [(CH₃NC₅H₃CHNC₆H₄OCH₃)PdCl(NCCH₃)]⁽¹⁺⁾*O₃SCF₃^(1-)=[(CH₃NC₅H₃CHNC₆H₄OCH₃)PdCl(NCCH₃)]O₃SCF₃(CAS DataBase Reference)
NIST Chemistry Reference: [(CH₃NC₅H₃CHNC₆H₄OCH₃)PdCl(NCCH₃)]⁽¹⁺⁾*O₃SCF₃^(1-)=[(CH₃NC₅H₃CHNC₆H₄OCH₃)PdCl(NCCH₃)]O₃SCF₃(1201000-52-3)
EPA Substance Registry System: [(CH₃NC₅H₃CHNC₆H₄OCH₃)PdCl(NCCH₃)]⁽¹⁺⁾*O₃SCF₃^(1-)=[(CH₃NC₅H₃CHNC₆H₄OCH₃)PdCl(NCCH₃)]O₃SCF₃(1201000-52-3)

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: 1201000-52-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1201000-52-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,0,0 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1201000-52:
(9*1)+(8*2)+(7*0)+(6*1)+(5*0)+(4*0)+(3*0)+(2*5)+(1*2)=43
43 % 10 = 3
So 1201000-52-3 is a valid CAS Registry Number.

1201000-52-3Upstream product

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1201000-52-3Relevant academic research and scientific papers

Modular syntheses of chiral and achiral C,N-chelated Pd(ii)-pyridinylidenes

Strong, Elizabeth T. J.,Price, Jacquelyn T.,Jones, Nathan D.

, p. 9123 - 9125 (2009)

Modular, high-yielding routes to achiral and chiral, C,N-chelated pyridinylidene complexes of Pd(ii) have been developed which rely on oxidative addition of either chloropyridinium imines or aldehydes to Pd(0), respectively, and, in the latter case, subsequent Schiff base formation with chiral primary amines. These protocols succinctly circumvent many of the problems currently associated with the synthesis of chelating pyridinylidenes.

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