70631-88-8

Basic information

• Product Name: 4-(3-fluoro-phenyl)-4-oxo-butyric acid
• Synonyms: Benzenebutanoic acid, 3-fluoro-;3-Fluorobenzenebutanoic acid;4-(3-FLUOROPHENYL)BUTANOIC ACID
• CAS NO: 70631-88-8
• Molecular Formula: C₁₀H₁₁FO₂
• Molecular Weight: 196.1750632
• EINECS: -0
• Mol File: 70631-88-8.mol
• Article Data: 14

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(3-fluoro-phenyl)-4-oxo-butyric acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3-fluoro-phenyl)-4-oxo-butyric acid(70631-88-8)
• EPA Substance Registry System: 4-(3-fluoro-phenyl)-4-oxo-butyric acid(70631-88-8)

Safety Data

• Hazardous Substances Data: 70631-88-8(Hazardous Substances Data)

Upstream product

• 1254715-20-2 C₁₅H₁₉FO₄ 
• 625-38-7 but-3-enoic acid 
• 768-35-4 3-fluorophenylboronic acid 
• 455-36-7 1-(3-fluorophenyl)ethanone 
• 456-48-4 3-Fluorobenzaldehyde 
• 51114-94-4 (2-carboxyethyl)triphenylphosphonium bromide 
• 462-06-6 fluorobenzene 
• 69797-46-2 4-(3'-fluorophenyl)-4-oxo-butanoic acid 
• 1231765-06-2 ethyl 4-(3-fluorophenyl)butanoate 
• 134464-81-6 C₁₁H₁₃FO₂ 
• 69797-47-3 4-(3-fluoro-phenyl)-4-oxo-butyric acid methyl ester 
• 127404-67-5 4-(3-fluoro-phenyl)-but-3-enoic acid 

Downstream Products

• 13790-88-0 7-fluoro-1-tetralone oxime 
• 2840-44-0 7-fluoro-3,4-dihydronaphthalen-1(2H)-one 
• 93742-85-9 5-fluoro-3,4-dihydronaphthalen-1(2H)-one 
• 1213300-76-5 (R)-(6-phenylsulfanyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-acetic acid methyl ester 
• 895534-22-2 (R)-(6-phenylsulfanyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-acetic acid 
• 895534-14-2 6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalene-1-carbonitrile 
• 895534-13-1 6-benzenesulfonyl-3,4-dihydro-naphthalene-1-carbonitrile 
• 895132-99-7 6-Benzenesulfonyl-3,4-dihydro-2H-naphthalen-1-one 
• 149915-80-0 6-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one 
• 880544-27-4 (6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-(4,5-dihydro-1H-imidazol-2-yl)-amine 
• 880544-30-9 C-(6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-methylamine 

Relevant articles and documents

COMPOSITIONS AND METHODS OF USING THE SAME FOR TREATMENT OF NEURODEGENERATIVE AND MITOCHONDRIAL DISEASE

The present disclosure is directed to adenine analogs, methods of making adenine analogs, and methods of treating disorders associated with PINK1 kinase activity including, but not limited to, neurodegenerative diseases, mitochondrial diseases, fibrosis,

Synthesis of Novel Pterocarpen Analogues via [3?+?2] Coupling-Elimination Cascade of α,α-Dicyanoolefins with Quinone Monoimines

By employing triethylamine as a catalyst, [3?+?2] coupling-elimination cascade of α,α-dicyanoolefins with quinone monoimines was realized. The reactions afforded various novel pterocarpen analogues with generally moderate yields (up to 75%). In addition, a plausible reaction mechanism was proposed.

SUBSTITUTED AROMATIC CARBOXAMIDE AND UREA DERIVATIVES AS VANILLOID RECEPTOR LIGANDS

The invention relates to substituted aromatic carboxamide and urea derivatives, to processes for the preparation thereof, to pharmaceutical compositions containing these compounds and also to the use of these compounds for preparing pharmaceutical compositions (formula (I)).