3,3,3-Trifluoroalanine methyl ester hydrochloride

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Reagent Code: #43874
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CAS Number 134297-36-2

science Other reagents with same CAS 134297-36-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.55 g/mol
Formula C₄H₇ClF₃NO₂
badge Registry Numbers
MDL Number MFCD08532471
thermostat Physical Properties
Melting Point 165.0℃(Solv: methanol (67-56-1))
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of fluorinated amino acids, which are crucial for developing peptide-based drugs. Its trifluoromethyl group enhances metabolic stability and bioavailability, making it valuable in creating therapeutic agents. Additionally, it is employed in organic synthesis to introduce fluorine atoms into target molecules, improving their chemical properties for various applications in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿31,356.00
inventory 250mg
10-20 days ฿3,402.00
inventory 1g
10-20 days ฿11,097.00

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3,3,3-Trifluoroalanine methyl ester hydrochloride
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of fluorinated amino acids, which are crucial for developing peptide-based drugs. Its trifluoromethyl group enhances metabolic stability and bioavailability, making it valuable in creating therapeutic agents. Additionally, it is employed in organic synthesis to introduce fluorine atoms into target molecules, improving their chemical properties for various applications in medicinal chemistry.

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of fluorinated amino acids, which are crucial for developing peptide-based drugs. Its trifluoromethyl group enhances metabolic stability and bioavailability, making it valuable in creating therapeutic agents. Additionally, it is employed in organic synthesis to introduce fluorine atoms into target molecules, improving their chemical properties for various applications in medicinal chemistry.

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