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4-Benzoyl-3-methoxyfuran-2(5H)-one is a chemical compound with the molecular formula C12H10O4. It is a derivative of furan-2(5H)-one, featuring a benzoyl group at the 4-position and a methoxy group at the 3-position. 4-benzoyl-3-methoxyfuran-2(5H)-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through chemical reactions involving furan derivatives and can be used as an intermediate in the preparation of more complex molecules. The compound's properties, such as its solubility and stability, can be influenced by the presence of the benzoyl and methoxy groups, making it a versatile building block in organic chemistry.

7478-50-4

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7478-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7478-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7478-50:
(6*7)+(5*4)+(4*7)+(3*8)+(2*5)+(1*0)=124
124 % 10 = 4
So 7478-50-4 is a valid CAS Registry Number.

7478-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzoyl-4-methoxy-2H-furan-5-one

1.2 Other means of identification

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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:7478-50-4 SDS

7478-50-4Relevant academic research and scientific papers

Substituted γ-Lactones: On the Structural Elucidation of the Reaction Products from 4-Aroyl-3-hydroxy-2(5H)-furanones and 1,2-Diamines

Zimmer, Hans,Amer, Adel,Ho, Douglas,Palmer-Sungail, R.

, p. 1501 - 1510 (2007/10/02)

The reaction pathway of 4-aroyl-3-hydroxy-2(5H)-furanones 1 with diamines depends on the nature of the amine as well as on the applied reaction conditions.Thus, the reaction of 1a-d with 5,6-diamino-1,3-dimethyluracil 5 led to the formation of two isomeri

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