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1,3,4,6,7,9-hexabromo-2,3,4,5,6,7,8,9-octahydro-1H-cyclopenta[e]-as-indacene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73255-12-6

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73255-12-6 Usage

Type of Compound

Highly brominated polycyclic aromatic hydrocarbon (PAH)

Physical State

Yellowish powder

Solubility

Insoluble in water, soluble in organic solvents

Applications

a. Field-effect transistors
b. Light-emitting diodes
c. Solar cells

Properties

a. High thermal stability
b. Electron-transport properties

Environmental Impact

Toxic and harmful to the environment

Health Risks

Potential carcinogenic effects

Handling and Disposal

Proper handling and disposal are essential to prevent harm to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 73255-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,5 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73255-12:
(7*7)+(6*3)+(5*2)+(4*5)+(3*5)+(2*1)+(1*2)=116
116 % 10 = 6
So 73255-12-6 is a valid CAS Registry Number.

73255-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,4,6,7,9-hexabromo-2,3,4,5,6,7,8,9-octahydro-1H-cyclopenta[e]-as-indacene

1.2 Other means of identification

Product number -
Other names 1H-Trindene,3,4,6,7,9-hexabromo-2,3,4,5,6,7,8,9-octahydro

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:73255-12-6 SDS

73255-12-6Upstream product

73255-12-6Relevant academic research and scientific papers

The Trindene Trianion

Katz, Thomas J.,Slusarek, Wojciech

, p. 1058 - 1063 (1980)

The lithium salt of the trindene trianion (6) is synthesized in four steps from cyclopentanone.Bromination and debromination, as summarized in Scheme III, convert trindane (octahydro-1H-trindene,14) into the dihydro-1H-trindenes,16a and 16b, and these with n-butyllithium in tetrahydrofuran give 6.The formation of the trianion is evidenced by quenching with deuterated water yielding the required trideuterio derivatives of 16a,b.When only 2 mol of n-butyllithium is used, the dianion 18 forms instead, as evidenced by reaction with deuterated water yielding molecules of 16a,b containing two allylic deuterium atoms.Sandwich molecules, assigned structures 19a,b, containing two irons, are produced when the dianion is combined with ferrous chloride, and only traces of sandwiches containing three iron atoms (presumably 9 with M = Fe) are detected in the corresponding rection product of 6.A product hoped for, polymer 5, could not be identified.The trindene trianion, although it contains multiple charges in one ?-electron system, is a favorable species because its rings are all five and six membered, because its highest occupied molecular orbital is low in energy, and because its lowest unoccupied molecular orbital is high in energy.

A Diels-Alder approach to trans-trisbicyclo[2.2.1]heptabenzene derivative

Gao, Zhong-Qiang,Wei, Jun-Fa,Shi, Xian-Ying,Yu, Jun

body text, p. 6126 - 6128 (2009/04/05)

A new route to the synthesis of a trans-tris(bicyclo[2.2.1]hexeno)benzene derivative, using Diels-Alder reaction as critical step, was investigated. The compound with six methoxycarbonyl groups was successfully synthesized in good yield without any organometallic reagents. Some useful by-products from dimethyl but-2-ynedioate were also isolated from the last step. Perhaps due to stereo-hindrance or electrostatic repulsion in the cis-isomer, trans-isomer was found to be the only isomer in the crystal and its structure was proved by X-ray diffraction.

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