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2-Propen-1-one, 1-(5-chloro-2-hydroxy-4-methylphenyl)-3-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24547-65-7

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24547-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24547-65-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,4 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24547-65:
(7*2)+(6*4)+(5*5)+(4*4)+(3*7)+(2*6)+(1*5)=117
117 % 10 = 7
So 24547-65-7 is a valid CAS Registry Number.

24547-65-7SDS

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 (E)-1-(5-Chloro-2-hydroxy-4-methyl-phenyl)-3-(4-methoxy-phenyl)-propenone

1.2 Other means of identification

Product number -
Other names -

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:24547-65-7 SDS

24547-65-7Downstream Products

24547-65-7Relevant academic research and scientific papers

Iodine-mediated direct synthesis of 3-iodoflavones

Patil, Avinash M.,Kamble, Dayanand A.,Lokhande, Pradeep D.

, p. 1299 - 1307 (2018/04/05)

Molecular iodine has been used for the regioselective, one pot, direct synthesis of 3-iodoflavones from 2′-allyloxy chalcones, 2′-hydroxy chalcones and flavones. Allyl deprotection, cyclization dehydrogenation and α-iodination of 2′-allyloxychalcones has been achieved in a single step to offer 3-iodoflavones.

New synthesis of flavanones catalyzed by L-proline

Chandrasekhar,Vijeender,Venkatram Reddy

, p. 6991 - 6993 (2007/10/03)

L-Proline is utilized as an efficient organocatalyst for the synthesis of substituted flavanones and chalcones in good yields. The efficiency of the catalyst was proved with a variety of substrates ranging from electron-deficient to electron-rich aryl aldehydes and 2-hydroxyacetophenones.

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