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5-Hydroxy-2,4-diphenyl-furan-3-one is a chemical compound with the molecular formula C16H12O3. It is a derivative of furan-3-one, featuring a hydroxyl group at the 5-position and two phenyl rings attached to the 2 and 4 positions. 5-hydroxy-2,4-diphenyl-furan-3-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can be used as an intermediate in the preparation of complex organic molecules, particularly those with potential biological activity. The compound's properties, such as its solubility and stability, can be influenced by the presence of the hydroxyl group and the phenyl substituents, making it a versatile building block in organic synthesis.

5435-01-8

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5435-01-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5435-01-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5435-01:
(6*5)+(5*4)+(4*3)+(3*5)+(2*0)+(1*1)=78
78 % 10 = 8
So 5435-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O3/c17-14-13(11-7-3-1-4-8-11)16(18)19-15(14)12-9-5-2-6-10-12/h1-10,15,18H

5435-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-2,4-diphenyl-2H-furan-5-one

1.2 Other means of identification

Product number -
Other names 5-hydroxy-2,4-diphenylfuran-3-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:5435-01-8 SDS

5435-01-8Downstream Products

5435-01-8Relevant academic research and scientific papers

REACTION OF O-TRIMETHYLSILYLATED CYANOHYDRINS WITH α-BROMOESTERS: A NEW SYNTHESIS OF TETRONIC ACIDS

Krepski, Larry R.,Lynch, Laurie E.,Heilmann, Steven M.,Rasmussem, Jerald K.

, p. 981 - 984 (2007/10/02)

Tetronic acids and β-keto-γ-butyrolactones are easily prepared by the zinc induced reaction of O-trimethylsilylated cyanohydrins and α-bromoesters.

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