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1,4-Pentanedione, 3-(4-chlorobenzoyl)-1-phenyl- is a chemical compound with the molecular formula C13H11ClO2. It is a derivative of pentanedione, featuring a 4-chlorobenzoyl group attached to the 3-position and a phenyl group at the 1-position. 1,4-Pentanedione, 3-(4-chlorobenzoyl)-1-phenyl- is known for its potential applications in the synthesis of various organic compounds and pharmaceuticals, particularly as an intermediate in the preparation of certain drugs and agrochemicals. Its structure provides a unique combination of functional groups, which can participate in various chemical reactions, such as condensations, substitutions, and rearrangements, making it a valuable building block in organic synthesis.

93078-47-8

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93078-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93078-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,7 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93078-47:
(7*9)+(6*3)+(5*0)+(4*7)+(3*8)+(2*4)+(1*7)=148
148 % 10 = 8
So 93078-47-8 is a valid CAS Registry Number.

93078-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorobenzoyl)-1-phenylpentane-1,4-dione

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

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More Details:93078-47-8 SDS

93078-47-8Downstream Products

93078-47-8Relevant academic research and scientific papers

DERIVES N-ARYL PYRROLIQUES A ACTIVITE ANALGESIQUE ET ANTI-INFLAMMATOIRE 2eme Partie - Pharmaco-modulation du modele aryl-1 pyrrole.

Thiault, G. A.,Le Guen, Y.,Boucherle, A.,Walrant, P.

, p. 765 - 780 (2007/10/02)

In order to increase the pharmacological activities of the molecules described in the first part of the paper, an acetic or a 2-propionic group was introduced in to the fondamental structure, either on the aromatic ring, on the pyrrole nitrogen or on carb

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