256417-11-5

Basic information

• Product Name: 2,3-Difluoro-4-methoxybenzaldehyde
• Synonyms: 2,3-Difluoro-4-methoxybenzaldehyde
• CAS NO: 256417-11-5
• Molecular Formula: C₈H₆F₂O₂
• Molecular Weight: 172.13
• Mol File: 256417-11-5.mol
• Article Data: 6

Chemical Properties

• Melting Point: 65-66 °C
• Boiling Point: 235.7°Cat760mmHg
• Flash Point: 93.7°C
• Appearance: /
• Density: 1.289g/cm³
• Vapor Pressure: 0.0494mmHg at 25°C
• Refractive Index: 1.506
• Storage Temp.: 2-8°C
• Sensitive: Air Sensitive
• CAS DataBase Reference: 2,3-Difluoro-4-methoxybenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Difluoro-4-methoxybenzaldehyde(256417-11-5)
• EPA Substance Registry System: 2,3-Difluoro-4-methoxybenzaldehyde(256417-11-5)

Safety Data

• Hazard Codes: Xi
• TSCA: No
• Hazardous Substances Data: 256417-11-5(Hazardous Substances Data)

Usage

Uses

use in drug synthesis.

InChI:InChI=1/C8H6F2O2/c1-12-6-3-2-5(4-11)7(9)8(6)10/h2-4H,1H3

Upstream product

• 4885-02-3 Dichloromethyl methyl ether 
• 134364-69-5 2.3-difluoroanisole 
• 6418-38-8 2,3-difluorophenol 
• 4394-85-8 4-morpholinecarboxaldehyde 
• 676500-39-3 2,3-difluoro-4-hydroxybenzaldehyde 
• 74-88-4 methyl iodide 
• 749230-30-6 (2,3-difluorophenoxy)triisopropylsilane 
• 1010800-88-0 2,3-difluoro-4-((triisopropylsilyl)oxy)benzoic acid 
• 1010801-00-9 2,3-difluoro-4-((triisopropylsilyl)oxy)benzaldehyde 
• 594-19-4 tert.-butyl lithium 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 689258-07-9 (2E)-3-(2,3-difluoro-4-methoxyphenyl)-N-methoxy-N-methylprop-2-enamide 
• 1010801-01-0 methyl 3-(2,3-difluoro-4-methoxyphenyl)-3-hydroxy-2,2-dimethylpropanoate 
• 676500-39-3 2,3-difluoro-4-hydroxybenzaldehyde 
• 931108-29-1 1-ethynyl-2,3-difluoro-4-methoxybenzene 
• 1355330-17-4 5-(2,3-difluoro-4-methoxyphenyl)-1-(3,4,5-trimethoxyphenyl)-1H-1,2,3-triazole 
• 1010801-02-1 methyl 3-(2,3-difluoro-4-methoxyphenyl)-2,2-dimethyl-3-oxopropanoate 
• 1010801-04-3 3-(2,3-difluoro-4-hydroxyphenyl)-4,4-dimethyl-1H-pyrazol-5(4H)-one 
• 1010802-00-2 C₂₉H₂₉F₅N₆O₄ 
• 1093857-65-8 2-[4-[2,3-Difluoro-4-(4,4-dimethyl-5-oxo-4,5-dihydro-1H-pyrazol-3-yl)phenoxy]butyl]-5-(8-methoxy-2-trifluoromethylimidazo[1,2-a]pyridin-5-yl)-4,4-dimethyl-2,4-dihydro-pyrazol-3-one 
• 1093857-58-9 2-[4-[2,3-difluoro-4-(4,4-dimethyl-5-oxo-4,5-dihydro-1H-pyrazol-3-yl)phenoxy]butyl]-5-(4-methoxy-2-trifluoromethylbenzo[d]thiazol-7-yl)-4,4-dimethyl-2,4-dihydro-pyrazol-3-one 
• 1010801-03-2 5-(2,3-Difluoro-4-methoxyphenyl)-4,4-dimethyl-2,4-dihydropyrazol-3-one 

Relevant articles and documents

GEMINAL SUBSTITUTED QUINUCLIDINE AMIDE COMPOUNDS AS AGONISTS OF ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTORS

The present invention relates to novel geminal substituted quinuclidine amide compounds, and pharmaceutical compositions of the same, that are suitable as agonists or partial agonists of α7- nAChR, and methods of preparing these compounds and compositions, and the use of these compounds and compositions in methods of maintaining, treating and/or improving cognitive function. In particular, methods of administering the compound or composition to a patient in need thereof, for example a patient with a cognitive deficiency and/or a desire to enhance cognitive function, that may derive a benefit therefrom.

Halogenated analogs of 1′-acetoxychavicol acetate, Rev-export inhibitor from Alpinia galanga, designed from mechanism of action

In the course of search for the robust analogs of 1′-acetoxychavicol acetate (ACA, 1), the Rev-export inhibitor from the medicinal plant Alpinia galanga, we clarified formation of the quinone methide intermediate ii to be essential for exerting the inhibi

Cycloalkyl alkanoic acids as integrin receptor antagonists derivatives

The present invention relates to a class of compounds represented by the Formula I or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising compounds of the Formula I, and methods of selectively inhibiting or antagonizing the αvβ3 and/or αvβ5 integrin.