Cas 1260103-96-5,Hg((C2H4O)5C2H4NC6H4CH(OH)C6H2(NO2)(OCH3)2)(ClO4)(1+)*ClO4(1-)=Hg((C2H4O)5C2H4NC6H4CH(OH)C6H2(NO2)(OCH3)2)(ClO4)2

1260103-96-5

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Basic information

Product Name: Hg((C₂H₄O)5C₂H₄NC₆H₄CH(OH)C₆H₂(NO₂)(OCH₃)2)(ClO₄)⁽¹⁺⁾*ClO₄^(1-)=Hg((C₂H₄O)5C₂H₄NC₆H₄CH(OH)C₆H₂(NO₂)(OCH₃)2)(ClO₄)2
Synonyms:
CAS NO:1260103-96-5
Molecular Formula:
Molecular Weight: 950.097
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: Hg((C₂H₄O)5C₂H₄NC₆H₄CH(OH)C₆H₂(NO₂)(OCH₃)2)(ClO₄)⁽¹⁺⁾*ClO₄^(1-)=Hg((C₂H₄O)5C₂H₄NC₆H₄CH(OH)C₆H₂(NO₂)(OCH₃)2)(ClO₄)2(CAS DataBase Reference)
NIST Chemistry Reference: Hg((C₂H₄O)5C₂H₄NC₆H₄CH(OH)C₆H₂(NO₂)(OCH₃)2)(ClO₄)⁽¹⁺⁾*ClO₄^(1-)=Hg((C₂H₄O)5C₂H₄NC₆H₄CH(OH)C₆H₂(NO₂)(OCH₃)2)(ClO₄)2(1260103-96-5)
EPA Substance Registry System: Hg((C₂H₄O)5C₂H₄NC₆H₄CH(OH)C₆H₂(NO₂)(OCH₃)2)(ClO₄)⁽¹⁺⁾*ClO₄^(1-)=Hg((C₂H₄O)5C₂H₄NC₆H₄CH(OH)C₆H₂(NO₂)(OCH₃)2)(ClO₄)2(1260103-96-5)

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: 1260103-96-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1260103-96-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,1,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1260103-96:
(9*1)+(8*2)+(7*6)+(6*0)+(5*1)+(4*0)+(3*3)+(2*9)+(1*6)=105
105 % 10 = 5
So 1260103-96-5 is a valid CAS Registry Number.

1260103-96-5Upstream product

1260103-52-3 (4,5-dimethoxy-2-nitrophenyl)[4-(1,4,7,10,13-pentaoxa-16-azacyclooctadec-16-yl)phenyl]methanol

1260103-96-5Downstream Products

1260103-52-3 (4,5-dimethoxy-2-nitrophenyl)[4-(1,4,7,10,13-pentaoxa-16-azacyclooctadec-16-yl)phenyl]methanol

1260103-96-5Relevant academic research and scientific papers

Buffering heavy metal ions with photoactive CrownCast cages

Mbatia, Hannah W.,Kennedy, Daniel P.,Camire, Casey E.,Incarvito, Christopher D.,Burdette, Shawn C.

, p. 5069 - 5078 (2010)

Historically, caged compounds have been used to interrogate the biological activity of organic molecules by using light; however, R. Tsien and others have developed methodologies over the last three decades for using nitrobenzyl-derived caged complexes to

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