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Pentacyclo[20.2.2.24,7.210,13.216,19]dotriaconta-4,6,10,12,16,18,22,24,25,27,29,31-dodecaene is a complex organic compound with the molecular formula C32H48. It is a polycyclic aromatic hydrocarbon, characterized by its unique structure consisting of five interconnected rings and twelve double bonds. Pentacyclo[20.2.2.24,7.210,13.216,19]dotriaconta-4,6,10,12,16,18,22,24,25,27,29,31-dodecaene(6CI,7CI,8CI,9CI) is of interest in the field of organic chemistry, particularly for its potential applications in materials science and as a precursor in the synthesis of other complex molecules. Due to its large size and intricate structure, it presents challenges in synthesis and characterization, making it a subject of study for chemists interested in exploring the limits of molecular architecture and reactivity.

283-81-8

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283-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 283-81-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 283-81:
(5*2)+(4*8)+(3*3)+(2*8)+(1*1)=68
68 % 10 = 8
So 283-81-8 is a valid CAS Registry Number.

283-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [24]paracyclophane

1.2 Other means of identification

Product number -
Other names Tetrakis[2.2.2]paraxylylen

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:283-81-8 SDS

283-81-8Downstream Products

283-81-8Relevant academic research and scientific papers

Samarium(II) Diiodide Mediated Coupling of Bis(bromomethyl)arenes. Facile Synthesis of n>Cyclophanes without using High-Dilution Techniques

Takahashi, Senji,Mori, Nobuo

, p. 2029 - 2032 (2007/10/02)

In the presence of samarium(II) diiodide (Sml2), coupling of 1,3- and 1,4-bis(bromomethyl)benzenes proceeds smoothly to give their cyclic and acyclic oligomers.Use of 1.2 equiv. of Sml2 gives 1,2-bis(3- and 4-bromomethylphenyl)ethanes, respectively, in 95percent yield, and the use of 5.0 equiv. of Sml2 affords n>metacyclophanes and n>paracyclpphanes (n = 2, 3 and 4), respectively, in satisfactory yields.By using 5.0 equiv. of Sml2, 2-bromo- and 2-methoxy-1,4-bis(bromomethyl)benzenes and 1,4- and 2,6-bis(bromomethyl)naphthalenes each give only one of several expected isomeric cyclophanes as the major cyclic oligomer.

Reductive Coupling by Chromium(0) - (Bibenzyl)- and (Stilbene)tricarbonylchromium(0) Complexes by a One-Pot Reaction from Benzylic Halides

Wey, Hans G.,Butenschoen, Holger

, p. 93 - 99 (2007/10/02)

Reaction of Cr(CO)3(NH3)3 with benzylic mono-, di-, and trihalides leads to the formation of 1,2-diarylethanes, -ethenes, and diphenylethyne in satisfactory yields.Di(halomethyl)benzene derivatives yield product mixtures containing both reduction products and coupling products.With a higher excess in chromium(0), under otherwise unchanged reaction conditions, the corresponding (arene)tricarbonylchromium(0) complexes of the coupling products are formed in a one-pot reaction from the benzylic halides.

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