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5,6,11,12,17,18-hexadehydrotribenzo[a,e,i][12]annulene is a complex organic compound characterized by its unique structure, which consists of three fused benzene rings forming a 12-membered annulene ring system. 5,6,11,12,17,18-hexadehydrotribenzo[a,e,i][12]annulene is notable for its extensive dehydrogenation, with 16 hydrogen atoms removed, leading to a highly unsaturated and conjugated π-electron system. The compound's name reflects its structure, with the numbers indicating the positions of the double bonds relative to the benzene rings. Due to its highly unsaturated nature, 5,6,11,12,17,18-hexadehydrotribenzo[a,e,i][12]annulene is likely to exhibit interesting electronic and optical properties, making it a subject of interest in the field of organic chemistry and materials science.

5385-26-2

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5385-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5385-26-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,8 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5385-26:
(6*5)+(5*3)+(4*8)+(3*5)+(2*2)+(1*6)=102
102 % 10 = 2
So 5385-26-2 is a valid CAS Registry Number.

5385-26-2SDS

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 AC1L3CWD

1.2 Other means of identification

Product number -
Other names Tribenzo[a,e,i]cyclododecene,5,6,11,12,17,18-hexadehydro

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:5385-26-2 SDS

5385-26-2Relevant academic research and scientific papers

Copper-mediated simple and efficient synthesis of tribenzohexadehydro[12] annulene and its derivatives

Iyoda, Masahiko,Sirinintasak, Siriwan,Nishiyama, Yoshihiro,Vorasingha, Anusorn,Sultana, Fatema,Nakao, Kazumi,Kuwatani, Yoshiyuki,Matsuyama, Haruo,Yoshida, Masato,Miyake, Yoshihiro

, p. 1527 - 1531 (2007/10/03)

A simple and efficient synthesis of tribenzohexadehydro[12]annulene and its derivatives was carried out using coupling reaction of acetylenes with iodoarenes in the presence of catalytic amounts of CuI and PPh3, together with three equivalents

Synthesis and structural and theoretical characterization of a nickel(0) complex of tribenzocyclyne (TBC) and the preparation of a novel organometallic conductor

Ferrara,Tanaka,Fierro,Tessier-Youngs,Youngs

, p. 2089 - 2098 (2008/10/08)

Reaction of Ni(COD)2 with TBC in benzene affords a planar nickel(0) complex, Ni(TBC), with the nickel atom coordinated equally by all three alkynes of the TBC ligand. The reaction chemistry of moderately reversible. Ni(TBC) is reduced with lithium, sodium, and potassium in various solvents (THF and DME) in the presence of various chelating agents (TMEDA, 18-crown-6, and cryptand-(2.2.2)) to the monoanion and dianion. The material [K(C222)]2[Ni(TBC)] was combined with Ni(TBC) to yield a conducting material. The maximum conductivity (via two-probe power compaction) was observed to be 2 × 10-3 (Ω cm)-1 at 0.5 electron per Ni(TBC) unit. A parallel study on TBC showed a maximum conductivity of 8 (2) × 10-5 (Ω cm)-1 at 0.6 electron per TBC unit.

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