Cas 141584-96-5,Cu(C34H34N2O6)(C41H40N2O6)(1+)*BF4(1-)={Cu(C34H34N2O6)(C41H40N2O6)}BF4

141584-96-5

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Basic information

Product Name: Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)⁽¹⁺⁾*BF₄^(1-)={Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)}BF₄
Synonyms: Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)⁽¹⁺⁾*BF₄^(1-)={Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)}BF₄
CAS NO:141584-96-5
Molecular Formula:
Molecular Weight: 1373.78
EINECS: N/A
Product Categories: N/A
Mol File: 141584-96-5.mol
Article Data: 1

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: Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)⁽¹⁺⁾*BF₄^(1-)={Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)}BF₄(CAS DataBase Reference)
NIST Chemistry Reference: Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)⁽¹⁺⁾*BF₄^(1-)={Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)}BF₄(141584-96-5)
EPA Substance Registry System: Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)⁽¹⁺⁾*BF₄^(1-)={Cu(C₃₄H₃₄N₂O₆)(C₄₁H₄₀N₂O₆)}BF₄(141584-96-5)

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: 141584-96-5(Hazardous Substances Data)

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141584-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141584-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,8 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141584-96:
(8*1)+(7*4)+(6*1)+(5*5)+(4*8)+(3*4)+(2*9)+(1*6)=135
135 % 10 = 5
So 141584-96-5 is a valid CAS Registry Number.

141584-96-5Upstream product

76871-59-5 1,14-diiodo-3,6,9,12-tetraoxatetradecane

141584-96-5Downstream Products

141584-96-5Relevant articles and documents

Synthesis, characterization, and a proton NMR study of topologically chiral copper(I) [2]-catenates and achiral analogues

Chambron, Jean-Claude,Mitchell, Dennis K.,Sauvage, Jean-Pierre

, p. 4625 - 4631 (2007/10/02)

Cu(I) catenates and the corresponding metal-free catenands in which one or both constitutive rings are oriented have been synthesized and characterized. Ring orientation is achieved by an appropriate substitution on the phenanthroline core of the macrocyc

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