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2(3H)-Furanone, dihydro-3-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

194724-89-5

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194724-89-5 Usage

Chemical structure

Furanone ring with a 4-methoxyphenyl group attached

Physical state

Colorless liquid

Odor

Sweet, caramel-like

Common uses

Production of flavorings and fragrances

Antimicrobial properties

Capable of killing or inhibiting the growth of microorganisms

Antioxidant properties

Able to prevent or slow down the oxidation of other substances

Health benefits

Potential anti-inflammatory and anti-cancer properties

Scientific research

Ongoing studies exploring its potential health benefits and uses

Appearance

Colorless liquid

Usage

Commonly used in food and cosmetic products

Safety concerns

Potential health risks may depend on concentration and exposure levels.

Check Digit Verification of cas no

The CAS Registry Mumber 194724-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,7,2 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 194724-89:
(8*1)+(7*9)+(6*4)+(5*7)+(4*2)+(3*4)+(2*8)+(1*9)=175
175 % 10 = 5
So 194724-89-5 is a valid CAS Registry Number.

194724-89-5SDS

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-(4-methoxyphenyl)oxolan-2-one

1.2 Other means of identification

Product number -
Other names 3-(4-methoxy-phenyl)-dihydro-furan-2-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:194724-89-5 SDS

194724-89-5Relevant academic research and scientific papers

Organocatalytic Gram-Scale Synthesis and Alkylation of Heteroaryl and Electron-Rich Aryl α-Substituted γ-Lactones

Bos, Maxence,Buttard, Floris,Riguet, Emmanuel,Vallée, Alexis

, p. 3151 - 3159 (2019/08/07)

The synthesis of γ-lactones α-substituted with heterocycles and electron-rich aromatic rings is described. The method, based on a sequence involving an organocatalytic addition of boronic acid to the 5-hydroxyfuran-2(5 H)-one, followed by reduction and lactonization, gives access to broad range of γ-lactones on a gram scale. Among these, γ-lactones bearing a benzofuran, a benzothiophene, and an indole ring were alkylated in mild catalytic conditions to construct α-quaternary stereocenters. Interesting mild oxidation reaction, using molecular oxygen, was also highlighted during this study.

Ni-Catalyzed Reductive C-O Bond Arylation of Oxalates Derived from α-Hydroxy Esters with Aryl Halides

Gao, Mengyu,Sun, Deli,Gong, Hegui

supporting information, p. 1645 - 1648 (2019/03/11)

A Ni-catalyzed reductive cross-coupling of α-hydroxycarbonyl compounds modified with oxalyl groups and aryl halides has been developed that furnishes α-aryl esters under mild conditions and tolerates a variety of functionalized aryl halides bearing electron-withdrawing and -donating groups. This work highlights C-O bond fragmentation on secondary alkyl carbon centers that generates α-carbonyl radicals.

SERINE/THREONINE KINASE INHIBITORS

-

Paragraph 00263, (2015/07/16)

Compounds of Formula I or a stereoisomer, tautomer or pharmaceutically acceptable salt thereof are provided, which are useful for the treatment of diseases. Methods of using compounds of Formula I or a stereoisomer, tautomer or pharmaceutically acceptable salt thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such diseases, or associated pathological conditions are disclosed.

Weak arene C-h×××o hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones

Huang, Zhiyan,Chen, Zuliang,Lim, Li Hui,Quang, Gia Chuong Phan,Hirao, Hajime,Zhou, Jianrong

supporting information, p. 5807 - 5812 (2013/07/05)

Weak force in action: In the title reaction, the palladium catalyst (see figure, left) uses weak CH×××O hydrogen bonding to control the absolute configuration of the new stereocenter. A similar palladium catalyst (right) used conventional NH×××O hydrogen bonding to guide stereoselection. Copyright

Enantioselective acylation of silyl ketene acetals through fluoride anion-binding catalysis

Birrell, James A.,Desrosiers, Jean-Nicolas,Jacobsen, Eric N.

supporting information; experimental part, p. 13872 - 13875 (2011/10/09)

A highly enantioselective acylation of silyl ketene acetals with acyl fluorides has been developed to generate useful α,α-disubstituted butyrolactone products. This transformation is promoted by a new thiourea catalyst and 4-pyrrolidinopyridine and represents the first example of enantioselective thiourea anion-binding catalysis with fluoride.

Regioselective hydroformylation of allylic alcohols

Lightburn, Thomas E.,De Paolis, Omar A.,Cheng, Ka H.,Tan, Kian L.

supporting information; experimental part, p. 2686 - 2689 (2011/06/28)

A highly regioselective hydroformylation of allylic alcohols is reported toward the synthesis of β-hydroxy-acid and aldehyde products. The selectivity is achieved through the use of a ligand that reversibly binds to alcohols in situ, allowing for a directed hydroformylation to occur. The application to trisubstituted olefins was also demonstrated, which yields a single diastereomer product consistent with a stereospecific addition of CO and hydrogen.

Catalytic hydrogenation of carboxamides and esters by well-defined Cp*Ru complexes bearing a protic amine ligand

Ito, Masato,Ootsuka, Takashi,Watari, Ryo,Shiibashi, Akira,Himizu, Akio,Ikariya, Takao

supporting information; experimental part, p. 4240 - 4242 (2011/06/21)

A novel catalytic method for the straightforward hydrogenation of carboxamides and esters to primary alcohols has been developed. Chiral modification in the ligand sphere of the well-defined Cp*Ru catalyst molecule opens up a new possibility for the development of an enantioselective hydrogenation of racemic substrates via dynamic kinetic resolution.

A novel estrogen receptor ligand template

Sibley, Robert,Hatoum-Mokdad, Holia,Schoenleber, Robert,Musza, Laszlo,Stirtan, William,Marrero, Diana,Carley, William,Xiao, Hong,Dumas, Jacques

, p. 1919 - 1922 (2007/10/03)

Three synthetic routes towards a novel estrogen receptor ligand template based on a rigid bicyclo-[3.3.1]-nonene core have been investigated. The prototype compound exhibits potent binding at the ERβ receptor and promising estrogen receptor subtype select

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