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63295-11-4

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63295-11-4 Usage

Chemical class

Furanone

Derivative

Dihydro derivative of 5,5-bis(4-fluorophenyl)furan-2(3H)-one

Potential applications

Pharmaceutical and agricultural industries

Bioactive properties

Antioxidant, antibacterial, and antifungal
Possible use as a flavor and fragrance ingredient

Ongoing research

Further investigation into potential applications and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 63295-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,9 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63295-11:
(7*6)+(6*3)+(5*2)+(4*9)+(3*5)+(2*1)+(1*1)=124
124 % 10 = 4
So 63295-11-4 is a valid CAS Registry Number.

63295-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-Bis(4-fluorphenyl)-4,5-dihydro-2(3H)-furanon

1.2 Other means of identification

Product number -
Other names 4,4-bis-(4-fluorophenyl)-4-butanolide

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:63295-11-4 SDS

63295-11-4Relevant articles and documents

Lactones, V: Synthesis of γ,γ-diaryl-γ-butyrolactones via 1,1-diarylethenes

Lehmann,Gajewski

, p. 754 - 757 (1985)

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Copper-Catalyzed Formal [2+2+1] Heteroannulation of Alkenes, Alkylnitriles, and Water: Method Development and Application to a Total Synthesis of (±)-Sacidumlignan D

Ha, Tu M.,Chatalova-Sazepin, Claire,Wang, Qian,Zhu, Jieping

supporting information, p. 9249 - 9252 (2016/08/05)

A copper-catalyzed three-component reaction of alkenes, alkylnitriles, and water affords γ-butyrolactones in good yields. The domino process involves an unprecedented hydroxy-cyanoalkylation of alkenes and subsequent lactonization with the creation of three chemical bonds and a quaternary carbon center. The synthetic potential of this novel [2+2+1] heteroannulation reaction was illustrated by a concise total synthesis of (±)-sacidumlignan D.

A Novel Friedel-Crafts Reaction: Synthesis of 4-Phenylnaphthalen-1-ols

Huang, Jai-Tung,Su, Tsann-Long,Watanabe, Kyoichi A.

, p. 4811 - 4815 (2007/10/02)

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