ChemicalBook--->CAS DataBase List--->1314008-27-9

1314008-27-9

1314008-27-9 Structure

1314008-27-9 Structure
IdentificationBack Directory
[Name]

Benzenemethanol,2-[(7,8-difluoro-2-methyl-3-quinolinyl)oxy]-6-fluoro-,-dimethyl-
[CAS]

1314008-27-9
[Synonyms]

Ipflufenoquin
Benzenemethanol,2-[(7,8-difluoro-2-methyl-3-quinolinyl)oxy]-6-fluoro-,-dimethyl-
[Molecular Formula]

C19H16F3NO2
[MOL File]

1314008-27-9.mol
[Molecular Weight]

347.331
Chemical PropertiesBack Directory
[Boiling point ]

442.225±45.00 °C(Press: 760.00 Torr)(predicted)
[density ]

1.316±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
[form ]

Solid
[pka]

13.959±0.29(predicted)
[color ]

Off-white to light yellow
[EPA Substance Registry System]

Benzenemethanol, 2-[(7,8-difluoro-2-methyl-3-quinolinyl)oxy]-6-fluoro-?,?-dimethyl- (1314008-27-9)
Safety DataBack Directory
[Symbol(GHS) ]

Environment (GHS09)
GHS09
[Signal word ]

Warning
[Hazard statements ]

H410
[Precautionary statements ]

P273-P391-P501
Hazard InformationBack Directory
[Uses]

Ipflufenoquin is used in the preparation of fungicidal compositions for the prevention and treatment of rice blast, and is suitable for the prevention and treatment of fungal diseases in rice, corn, fruits and vegetables.
[Definition]

ChEBI: Ipflufenoquin is a member of the class of quinolines that is quinoline substituted by a methyl group, 3-fluoro-2-(2-hydroxypropan-2-yl)phenoxy group, fluoro group and fluoro group at positions 2, 3, 7 and 8, respectively. It is a fungicide being developed by Nippon-Soda Co. Ltd (Japan) which has stable efficacy against a wide range of plant diseases, such as gray mold, scab and rice blast. It has a role as a fungicide. It is a member of quinolines, an organofluorine compound, an aromatic ether and a member of benzyl alcohols.
[Production Methods]

Ipflufenoquin is manufactured through a modular small-molecule route typical of modern quinoline-based fungicides: producers first build the substituted quinoline core from halogenated aniline and beta ketoester precursors via cyclisation, then introduce the key fluoroalkyl and ether substituents through controlled nucleophilic substitution or metal-catalysed coupling steps. The side-chain alcohol is installed late in the sequence to minimise degradation, followed by final oxidation or protection-deprotection steps to deliver the fully elaborated scaffold. After crude isolation, the active ingredient undergoes purification, crystallisation and quality control before being formulated into agricultural products.
[Mechanism of action]

Dihydroorotate dehydrogenase (DHODH) inhibitor
[Pesticide Type]

Fungicide
1314008-27-9 suppliers list
Company Name: BOC Sciences
Tel: +1-631-485-4226
Website: https://www.bocsci.com/
Company Name: Suzhou ARTK Medchem Co., Ltd.
Tel: +86-18168183658 , +86-18168183658
Website:
Company Name: ACE BIOSCIENCES  
Tel: +91-9395105396
Website: www.acebiosciences.in
Company Name: Shanghai Beckham Medical Technology Co., Ltd  
Tel: 13816613772
Website: https://www.chemicalbook.com/ShowSupplierProductsList16976/0_EN.htm
Company Name: Chongqing Chemieliva Pharmaceutical Co., Ltd.  
Tel: 18696571988
Website: http://www.chemieliva.com
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Website: https://www.targetmol.cn/
Company Name: Shanghai Kaisen Biotechnology Co., Ltd  
Tel: 17558870519
Website: https://coa.ikekule.com/
Company Name: Zhejiang Huida Biotech Co., Ltd.  
Tel: 0571-89903022 18679456698
Website: www.huidacollection.cn
Company Name: Guangzhou Baide Biotechnology Co., Ltd.  
Tel: 18925065404
Website: www.chemicalbook.com/ShowSupplierProductsList1802487/0_EN.htm
Tags:1314008-27-9 Related Product Information