Cas 207971-17-3,(C6H13)3Si(CCZn(CC4H2NC(C6H3(C(CH3)3)2)C4H2N)2CC)C6H4(CCZn(CC4H2NC(C6H3(C(CH3)3)2)C4H2N)2CC)Si(C6H13)3

207971-17-3

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Product Name: (C₆H₁₃)3Si(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)C₆H₄(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)Si(C₆H₁₃)3
Synonyms: (C₆H₁₃)3Si(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)C₆H₄(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)Si(C₆H₁₃)3
CAS NO:207971-17-3
Molecular Formula:
Molecular Weight: 2236.06
EINECS: N/A
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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: (C₆H₁₃)3Si(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)C₆H₄(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)Si(C₆H₁₃)3(CAS DataBase Reference)
NIST Chemistry Reference: (C₆H₁₃)3Si(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)C₆H₄(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)Si(C₆H₁₃)3(207971-17-3)
EPA Substance Registry System: (C₆H₁₃)3Si(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)C₆H₄(CCZn(CC₄H₂NC(C₆H₃(C(CH₃)3)2)C₄H₂N)2CC)Si(C₆H₁₃)3(207971-17-3)

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: 207971-17-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 207971-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,9,7 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 207971-17:
(8*2)+(7*0)+(6*7)+(5*9)+(4*7)+(3*1)+(2*1)+(1*7)=143
143 % 10 = 3
So 207971-17-3 is a valid CAS Registry Number.

207971-17-3Upstream product

207971-17-3Downstream Products

207971-17-3Relevant academic research and scientific papers

Enhanced electronic conjugation in anthracene-linked porphyrins

Taylor, Peter N.,Wylie, Andrew P.,Huuskonen, Juhani,Anderson, Harry L.

, p. 986 - 989 (2007/10/03)

Despite their larger separation, the porphyrin groups in 1 are more strongly conjugated than in analogous compounds in which butadiyne is the bridging unit. This stronger electronic coupling in 1 results in a bathochromic shift in its absorption and emission spectra.

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