2-AMINO-3-FLUOROBUTYRIC ACID

Base Information

• Chemical Name: 2-AMINO-3-FLUOROBUTYRIC ACID
• CAS No.: 50885-01-3
• Molecular Formula: C4H8FNO2
• Molecular Weight: 121.111
• Hs Code.: 2922498590
• Mol file: 50885-01-3.mol

Synonyms:2-Amino-3-fluorobutyric acid;2-Amino-3-fluorobutanoic acid;

Chemical Property of 2-AMINO-3-FLUOROBUTYRIC ACID

Chemical Property:

• Vapor Pressure: 0.00782mmHg at 25°C
• Melting Point: 186-187 °C
• Refractive Index: 1.433
• Boiling Point: 248.3 °C at 760 mmHg
• PKA: 1.89±0.10(Predicted)
• Flash Point: 104 °C
• PSA: 63.32000
• Density: 1.222 g/cm³
• LogP: 0.45660

Purity/Quality:

99% ^*data from raw suppliers

2-Amino-3-fluorobutyricacid ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Safety Statements: 24/25

MSDS Files:

Useful:

Technology Process of 2-AMINO-3-FLUOROBUTYRIC ACID

There total 5 articles about 2-AMINO-3-FLUOROBUTYRIC ACID which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

benzyl 2-(4,5-diphenyl-2-oxo-4-oxazolin-3-yl)-3-fluorobutanoate (110353-88-3,110353-89-4) → 3-fluoro-2-amino-butyric acid (50885-01-3)

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethanol; under 2327.2 Torr;

DOI:10.1021/jo00230a033

Reference yield:

2-Bromo-3-fluoro-butyric acid (50884-93-0) → 3-fluoro-2-amino-butyric acid (50885-01-3)

Guidance literature:

With ammonia;

DOI:10.1021/jm00270a022

Reference yield:

2-Amino-3-fluoro-butyronitrile → 3-fluoro-2-amino-butyric acid (50885-01-3)

Guidance literature:

With water; hydrogen cation; Heating;

DOI:10.1016/S0022-1139(00)85554-2

upstream raw materials:

L-threonine

2-Bromo-3-fluoro-butyric acid

benzyl 2-(4,5-diphenyl-2-oxo-4-oxazolin-3-yl)-3-fluorobutanoate

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