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42523-15-9

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42523-15-9 Usage

Appearance

White to yellow crystalline solid.

Solubility

Insoluble in water; soluble in organic solvents.

Usage

Building block for the synthesis of various organic compounds.

Applications

Potential pharmaceutical and industrial applications.

Hazards

Harmful if ingested, inhaled, or absorbed through the skin; may cause irritation to the eyes, skin, and respiratory system.

Safety Precautions

Handle and store with care; use proper protective equipment and procedures.

Check Digit Verification of cas no

The CAS Registry Mumber 42523-15-9 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, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42523-15:
(7*4)+(6*2)+(5*5)+(4*2)+(3*3)+(2*1)+(1*5)=89
89 % 10 = 9
So 42523-15-9 is a valid CAS Registry Number.

42523-15-9SDS

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-methoxyfluoren-9-one

1.2 Other means of identification

Product number -
Other names 1-methoxy-9-fluorenone

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:42523-15-9 SDS

42523-15-9Relevant articles and documents

Decarboxylative C-H arylation of benzoic acids under radical conditions

Seo, Sangwon,Slater, Mark,Greaney, Michael F.

, p. 2650 - 2653 (2012/07/27)

A decarboxylative radical cyclization reaction has been developed for the synthesis of fluorenones. The reaction uses Ag(I)/K2S 2O8 to oxidatively decarboxylate an aroylbenzoic acid to an aryl radical, which undergoes cyclization to afford fluorenone products in good yield.

Palladium-catalyzed annulation of arynes by 2-halobenzaldehydes: Synthesis of fluoren-9-ones

Zhang, Xiaoxia,Larock, Richard C.

, p. 3973 - 3976 (2007/10/03)

(Chemical Equation Presented) Arynes, generated in situ from 2-(trimethylsilyl)aryl triflates and CsF, undergo annulation by o-haloarenecarboxaldehydes in the presence of a Pd catalyst, providing a useful new method for the synthesis of fluoren-9-ones in good yields.

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