38102-67-9

Basic information

• Product Name: 4-(3-METHOXYPHENYL)-4-OXOBUTYRIC ACID
• Synonyms: 4-(3-METHOXYPHENYL)-4-OXOBUTYRIC ACID
• CAS NO: 38102-67-9
• Molecular Formula: C₁₁H₁₂O₄
• Molecular Weight: 208.21
• Mol File: 38102-67-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 105-107°C
• Boiling Point: 391°C at 760 mmHg
• Flash Point: 154.8°C
• Appearance: /
• Density: 1.206g/cm³
• Vapor Pressure: 8.13E-07mmHg at 25°C
• Refractive Index: 1.535
• CAS DataBase Reference: 4-(3-METHOXYPHENYL)-4-OXOBUTYRIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3-METHOXYPHENYL)-4-OXOBUTYRIC ACID(38102-67-9)
• EPA Substance Registry System: 4-(3-METHOXYPHENYL)-4-OXOBUTYRIC ACID(38102-67-9)

Safety Data

• Hazardous Substances Data: 38102-67-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H12O4/c1-15-9-4-2-3-8(7-9)10(12)5-6-11(13)14/h2-4,7H,5-6H2,1H3,(H,13,14)

Upstream product

• 108-30-5 succinic acid anhydride 
• 1711-05-3 m-anisoyl chloride 
• 105-36-2 ethyl bromoacetate 
• 100-66-3 methoxybenzene 
• 1115-30-6 diethyl acetylsuccinate 
• 6328-00-3 4-(3-nitro-phenyl)-4-oxo-butyric acid 
• 2051-95-8 succinylbenzene 
• 56872-07-2 4-(3-hydroxy-phenyl)-4-oxo-butyric acid 
• 77-78-1 dimethyl sulfate 
• 38102-72-6 4-oxo-4-(3-methoxyphenyl)butanenitrile 

Downstream Products

• 1017-06-7 6-(4-Methoxyphenyl)-4,5-dihydro-2H-pyridazin-3-one 
• 1427435-37-7 7-(4-methoxyphenyl)-3,4,8,9-tetrahydro-2H-pyridazino[1,6-a][1,3,5]triazin-2-imine 
• 1445852-90-3 C₁₂H₁₄N₂O₃ 
• 1427435-38-8 7-(4-methoxyphenyl)-3,4,8,9-tetrahydro-2H-pyridazino[1,6-a][1,3,5]triazin-2-one 
• 1427435-39-9 7-(4-methoxyphenyl)-3,4,8,9-tetrahydro-2H-pyridazino[1,6-a][1,3,5]triazin-2-thione 
• 6836-19-7 7-Methoxy-1-tetralone 
• 20175-97-7 7-methoxy-3,4-dihydronaphthalen-1(2H)-one oxime 
• 38102-79-3 (+)-(R)-γ-(3-methoxyphenyl)-γ-butyrolactone 
• 1283458-79-6 C₁₇H₁₇NO₃ 
• 38102-68-0 rac-5-(3-methoxyphenyl)dihydrofuran-2(3H)-one 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 
• 692728-90-8 4-(4-fluoro-benzyl)-6-methoxy-3,4-dihydro-2H-naphthalen-1-one 

Relevant articles and documents

Highly enantioselective [3+2] coupling of cyclic enamides with quinone monoimines promoted by a chiral phosphoric acid

Enantioselective [3+2] coupling of cyclic enamides with quinone monoimines was realised using a chiral phosphoric acid as a catalyst. This transformation allowed for the synthesis of highly enantioenriched polycyclic 2,3-dihydrobenzofurans (up to 99.9% ee). The absolute configuration of one product was determined by an X-ray crystal structural analysis. We also found a possible mechanism for this reaction.

THIOTRIAZOLYL DERIVATIVES

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