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1,4a,6a,6b-Tetrahydrocyclopenta[cd]pentalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89032-66-6

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89032-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89032-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,3 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89032-66:
(7*8)+(6*9)+(5*0)+(4*3)+(3*2)+(2*6)+(1*6)=146
146 % 10 = 6
So 89032-66-6 is a valid CAS Registry Number.

89032-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name isotriquinacene

1.2 Other means of identification

Product number -
Other names (4aS,6aS,6bS)-1,4a,6a,6b-Tetrahydro-cyclopenta[cd]pentalene

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:89032-66-6 SDS

89032-66-6Downstream Products

89032-66-6Relevant academic research and scientific papers

General Approach to the Synthesis of Poliquinenes. 8. Synthesis of Triquinacene, 1,10-Dimethyltriquinacene, and 1,10-Cyclohexanotriquinacene

Gupta, Ashok K.,Lannoye, Greg S.,Kubiak, Greg,Schkeryantz, Jeff,Wehrli, Suzanne,Cook, James M.

, p. 2169 - 2179 (2007/10/02)

The synthesis of tricyclo4,10>deca-2,5,8-triene (1), 1,10-dimethyltricyclo4,10>deca-2,5,8-triene (3), and tetracyclo1,8.04,8>tetradeca-2,5,13-triene (4) has been accomplished via the reaction of 1,2-dicarbonyl compounds with di-tert-butyl 3-oxoglutarate (Weiss reaction).Condensation of glyoxal 5a with di-tert-butyl 3-oxoglutarate (6b) gave the tetra-tert-butyl cis-dioxobicyclooctane-2,4,6,8-tetracarboxylate 7b in 93percent yield.This bisenol 7b was converted into the bisenol ether 9b regiospecifically (90percent yield).This transformation was followed by monoalkylation (KH, allyl iodide; -58 deg C) and hydrolysis to generate 2-allyl-cis-bicyclooctane-3,7-dione in 90percent overall yield from 9b.The mixture of epimiric 2-allyl-3,7-diones 11a,b was transformed (O3; DMS) into the mixture of epimiric aldehydes 12a,b.This process was followed by aldol cyclization (2 N HCl, THF) to provide the diastereomeric mixture of of endo-(13a) and exo-(13b) triquinane monols in 85percent yield.Reduction of 13a,b with borane-THF (0 deg C) generated the stereoisomeric mixture of triols 14a,b which were subjected to an HPMA-mediated dehydration sequence to provide triquinacene (1), accompanied by small amounts of isotriquinacene.The mixture of trienes were converted into pure 1 by exposure to p-TSA in methylene chloride-pentane.Substitution of biacetyl (5b) for glyoxal 5a in the Weiss reaction, followed by the analogous steps detailed in the synthesis of 1, provided 1,10-dimethyltriquinacene (3).In addition, the synthesis of 1,10-cyclohexanotriquinacene (4), another centro-substituted triquinacene, has been accomplished by substitution of cyclohexane-1,2-dione (23) for 5a in the condensation, followed by the same sequence of reactions presented above for 1 and 3.

THE SYNTHESIS OF TRIQUINACENE VIA THE WEISS REACTION.

Bertz, Steven H.,Lannoye, G.,Cook, J. M.

, p. 4695 - 4698 (2007/10/02)

A short, simple preparation of triquinacene 1 is based on four key steps: the Weiss reaction, high-yield monoalkylation of the resulting bicyclo system, aldol cyclization of aldehyde 6 and HMPA-mediated dehydration of triol 8.

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