Tetraphenylcyclopentadienone. UV 2019-01-05

Tetraphenylcyclopentadienone Rating: 4,1/10 505 reviews

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tetraphenylcyclopentadienone

. Copyright © 1921-2019 by Organic Syntheses, Inc. Appendix Chemical Abstracts Nomenclature Collective Index Number ; Registry Number Desoxybenzoin benzaldiphenylmaleide methylenedesoxybenzoin ethanol 64-17-5 Benzene 71-43-2 formaldehyde 50-00-0 Benzil 134-81-6 potassium hydroxide 1310-58-3 Phenylmagnesium bromide 100-58-3 dibenzyl ketone 102-04-5 Tetraphenylcyclopentadienone, Cyclopentadienone, tetraphenyl- 479-33-4 Follow Us via Published by Organic Syntheses, Inc. No part of this Website or Database may be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, mechanical, photocopying, recording, scanning or otherwise, except as permitted under Sections 107 or 108 of the 1976 United States Copyright Act. The flask is fitted with a reflux condenser, the temperature of the solution is raised nearly to the boiling point, and a solution of 3 g. These procedures must be conducted at one's own risk.

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tetraphenylcyclopentadienone

I have read and acknowledge that I have training in the field of organic chemistry and that Organic Syntheses does not warrant or guarantee safety in the use of these procedures. The product melts at 218—220° and weighs 35—37 g. The dark crystalline product is filtered with suction and washed with three 10-ml. When the frothing has subsided the mixture is refluxed for 15 minutes and then cooled to 0°. . . .

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