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Benzene, 1,1',1'',1'''-(1,2,3,4-cyclobutanetetrayl)tetrakis-, also known as cubane, is a unique organic compound with a highly symmetrical structure. It consists of four benzene rings connected by four ethylene bridges, forming a cubic arrangement. This molecule is characterized by its high stability and resistance to chemical reactions, making it an interesting subject for study in organic chemistry. The synthesis of cubane is challenging due to its complex structure, but it has been achieved through various methods, including the use of transition metal catalysts. The compound has potential applications in materials science and as a precursor for other complex organic molecules.

806-90-6

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806-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 806-90-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,0 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 806-90:
(5*8)+(4*0)+(3*6)+(2*9)+(1*0)=76
76 % 10 = 6
So 806-90-6 is a valid CAS Registry Number.

806-90-6SDS

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 (2,3,4-triphenylcyclobutyl)benzene

1.2 Other means of identification

Product number -
Other names 1,2,3,4-tetraphenylcyclobutane

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:806-90-6 SDS

806-90-6Upstream product

806-90-6Downstream Products

806-90-6Relevant academic research and scientific papers

Picosecond Dynamics of trans-Stilbene Photodimerization

Peters, Kevin S.,Freilich, Steven C.,Lee, Joseph

, p. 5482 - 5485 (2007/10/02)

Picosecond absorption spectroscopy is used to examine the dynamics of the 2+2 photodimerization reaction of trans-stilbene in benzene.The quenching of the first excited singlet state of trans-stilbene by ground-state trans-stilbene occurs at the diffusion limit, 2.03 * 1010 M-1 s-1.Upon quenching, a new intermediate is formed with a λmax of 480 nm which is characteristic of the charge-transfer species.The rate of the decay of the transient species is (2.40 +/- 0.37) * 109 s-1.The assignment of the transient to the excimer or a biradicaloid species at the pericyclic minimum is discussed.

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