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Tricyclo[8.2.2.24,7]hexadeca-4,6,10,12,13,15-hexaene-5,6,11,12-t is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53922-63-7

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53922-63-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53922-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53922-63:
(7*5)+(6*3)+(5*9)+(4*2)+(3*2)+(2*6)+(1*3)=127
127 % 10 = 7
So 53922-63-7 is a valid CAS Registry Number.

53922-63-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,2]paracyclophane-4,5,12,13-tetracarbonitrile

1.2 Other means of identification

Product number -
Other names 4,5,12,13-tertacyano[2.2]paracyclophane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53922-63-7 SDS

53922-63-7Downstream Products

53922-63-7Relevant academic research and scientific papers

Anti-[2.2](1,4)phthalocyaninophane: Spectroscopic evidence for transannular interaction in the excited states

Asano, Yoshiaki,Muranaka, Atsuya,Fukasawa, Akira,Hatano, Terutaka,Uchiyama, Masanobu,Kobayashi, Nagao

, p. 4516 - 4517 (2007)

The design and synthesis of a novel type of bisphthalocyanines, anti-[2.2](1,4)phthalocyaninophanes, were reported. The phthalocyanine dimer exhibited significantly split and red-shifted absorption in the near-IR region and maintained the fluorescence properties of phthalocyanines. The origin of the electronic communication between the two phthalocyanines was rationalized on the basis of the MO model analysis. Copyright

Weak C - H ... N≡ C hydrogen bonds in the structures of two poly(cyano)-substituted ring systems

Jones, Peter G.,Hopf, Henning,Mlynek, Cornelia,Swaminathan, Vijay Narayanan

, p. o723-o725 (2008/09/18)

In benzene-1,2,3-tricarbonitrile, C9H3N3, the packing of the two independent mol-ecules is three-dimensional and complex, involving inter alia bifurcated (C - H)2...N systems from neighbouring CH groups. In [2.2]paracyclo-phane-4,5,12,13-tetra-carbonitrile, C20H12N4, the [2.2]paracyclo-phane systems display the usual distortions, namely lengthened C - C bonds and widened sp 3 angles in the bridges, narrow angles in the six-membered rings at the bridgehead atoms, and flattened boat conformations of the rings. The mol-ecules are linked by a series of C - H...N inter-actions to form layers parallel to the ab plane. International Union of Crystallography 2007.

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