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42523-22-8

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42523-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42523-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,2 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42523-22:
(7*4)+(6*2)+(5*5)+(4*2)+(3*3)+(2*2)+(1*2)=88
88 % 10 = 8
So 42523-22-8 is a valid CAS Registry Number.

42523-22-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dihydroxy-9H-fluoren-9-one

1.2 Other means of identification

Product number -
Other names 1,4-Dihydroxy-fluoren-9-one

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:42523-22-8 SDS

42523-22-8Relevant articles and documents

Cu(I)-catalyzed intramolecular cyclizations of substituted 2-iodobenzophenones under thermal and microwave conditions

Haggam, Reda A.

, p. 6488 - 6494 (2013/07/26)

Novel, easy-to-perform and practical intramolecular Cu(I)-catalyzed cyclizations of substituted 2-iodobenzophenones under thermal and microwave conditions are reported. The isolated cyclized products under microwave conditions are obtained with high yields and with short reaction times offering a valuable and reliable alternative to other protocols for the synthesis of fluorene analogues.

An efficient synthesis of dihydroxyfluorenones via in situ Pd(0)-catalyzed cross-coupling

Ciske, Fred L.,Jones Jr., Winton D.

, p. 1195 - 1198 (2007/10/03)

All six dimethoxyfluorenones 6a-f and dihydroxyfluorenones 7a-f, wherein substitution occurs at only one aromatic ring, were conveniently prepared by palladium(0)-catalyzed cross-coupling reactions of aryl bromides/triflates 2a-e with in situ generated ar

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