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"15,16-Diazatricyclo[9.3.1.14,8]hexadeca-1(15),4,6,8(16),11,13-hexaene" is a complex organic compound with a unique molecular structure. It is a tricyclic amine, characterized by its three interconnected rings and multiple double bonds. 15,16-Diazatricyclo[9.3.1.14,8]hexadeca-1(15),4,6,8(16),11,13-hexaene is composed of 15 carbon atoms, 12 hydrogen atoms, and 2 nitrogen atoms, arranged in a specific pattern that gives it its name. The numbering of the carbon atoms in the name reflects the positions of the double bonds and the nitrogen atoms within the molecule. This chemical is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its structural complexity and the presence of nitrogen atoms, which can participate in a variety of chemical reactions.

6574-83-0

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6574-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6574-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6574-83:
(6*6)+(5*5)+(4*7)+(3*4)+(2*8)+(1*3)=120
120 % 10 = 0
So 6574-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2/c1-3-11-7-9-13-5-2-6-14(16-13)10-8-12(4-1)15-11/h1-6H,7-10H2

6574-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name anti-4,12-diaza<22>(1,3)cyclophane

1.2 Other means of identification

Product number -
Other names 1,4(2,6)-dipyridina-cyclohexaphane

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:6574-83-0 SDS

6574-83-0Relevant academic research and scientific papers

Synthesis, X-ray Structure, Basicity, and Dynamic Stereochemistry of a Donor-Substituted (2,6)Pyridinophane

Voegtle, Fritz,Koersgen, Ute Ursula,Puff, Heinrich,Reuter, Hans

, p. 343 - 346 (2007/10/02)

Treatment of 4b with phenyllithium afforded the donor-substituted 7,15-dimethoxy(2,6)pyridinophane (2) by intermolecular cyclization. 2 is compared with the unsubstituted compound 1 by X-ray crystallography, determination of basicity, and 1H-NMR studies.The results indicate an attractive interaction between the pyridine nitrogen of 2 and a H atom of a second molecule of 2. - Keywords: Pyridinophanes/ Pyridines, basicity of

A NEW SYNTHETIC METHOD OF CYCLOPHANES

Takemura, Hiroyuki,Shinmyozu, Teruo,Inazu, Takahiko

, p. 1031 - 1032 (2007/10/02)

Diazacyclophanes were converted to the correspondingcyclophanes via their N-nitroso derivatives by reductive extrusion of nitrogens.This reaction is simple, clean and mild, and may be an alternative synthetic way of cyclophanes.

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