885275-89-8

Basic information

• Product Name: N-(3-FLUOROPHENYL)-3-AMINOPROPIONIC ACID
• Synonyms: N-(3-FLUOROPHENYL)-3-AMINOPROPIONIC ACID;ASISCHEM D77546;OTAVA-BB 1142581;UKRORGSYN-BB BBV-215960;3-[(3-Fluorophenyl)amino]propionic acid;N-(3-Fluorophenyl)-b-alanine
• CAS NO: 885275-89-8
• Molecular Formula: C₉H₁₀FNO₂
• Molecular Weight: 183.18
• Mol File: 885275-89-8.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: N-(3-FLUOROPHENYL)-3-AMINOPROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-FLUOROPHENYL)-3-AMINOPROPIONIC ACID(885275-89-8)
• EPA Substance Registry System: N-(3-FLUOROPHENYL)-3-AMINOPROPIONIC ACID(885275-89-8)

Safety Data

• Hazardous Substances Data: 885275-89-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
N-(3-FLUOROPHENYL)-3-AMINOPROPIONIC ACID is used as a key intermediate in the synthesis of new drugs for various medical conditions, leveraging its ability to modulate neurotransmitter levels in the brain. This property makes it instrumental in the development of treatments for neurological and psychiatric disorders.
Used in Agrochemical Industry:
N-(3-FLUOROPHENYL)-3-AMINOPROPIONIC ACID is utilized as a building block in the creation of agrochemicals, contributing to the development of innovative products for agricultural applications, such as pesticides and herbicides.
Used in Medicinal Chemistry Research:
As a valuable tool in medicinal chemistry, N-(3-FLUOROPHENYL)-3-AMINOPROPIONIC ACID aids researchers in understanding the structure-activity relationships of compounds and in the design of novel therapeutic agents.
Used in Neuroscience Research:
In the field of neuroscience, N-(3-FLUOROPHENYL)-3-AMINOPROPIONIC ACID is employed to study the mechanisms of neurotransmission and to explore the potential of new compounds in treating brain-related disorders.

Upstream product

• 372-19-0 meta-fluoroaniline 
• 79-10-7 acrylic acid 

Downstream Products

• 1095270-78-2 5-fluoro-2,3-dihydro-1H-quinolin-4-one 
• 114417-35-5 7-fluoro-2,3-dihydro-1H-quinolin-4-one 
• 1257556-55-0 C₂₁H₂₅N₃O₃S 

Relevant articles and documents

1-(Arylsulfonyl)-2,3-dihydro-1H-quinolin-4-one derivatives as 5-HT 6 serotonin receptor ligands

Piperazinyl derivatives of 1-(arylsulfonyl)-2,3-dihydro-1H-quinolin-4-ones have been identified with high binding affinities for 5-HT6 receptor. In particular, 2-methyl-5-(N-methyl-piperazin-1-yl)-1-(naphthalene-2-sulfonyl)- 2,3-dihydro-1H-quinolin-4-one (8g) exhibits high binding affinity toward 5-HT6 (IC50 = 8 nM) receptor with good selectivity over other serotonin and dopamine receptors.

COMPOUND HAVING 11 ?-HSD1 INHIBITORY ACTIVITY

The present invention provides compounds having excellent 11β-HSD1 inhibitory activity. A compound represented by the following formula (I): [wherein X1 represents an oxygen atom, or the formula -(CR11R12)p-, etc., Y1 represents a hydrogen atom, a hydroxyl group, etc., Z1 represents an oxygen atom or the formula -(NR14)-, R1 represents a hydrogen atom, a halogen atom, a cyano group, a C1-4 alkyl group, a C1-4 alkyl group substituted with 1 to 3 halogen atoms, a C1-4 alkoxy group, a C1-4 alkoxycarbonyl group, a carboxyl group, a carbamoyl group, or an amino group, and m represents an integer of 1 or 2, and R2 represents a hydrogen atom or a C1-4 alkyl group, and n represents an integer of 1 or 2].