(3S)-3-(Difluoromethyl)pyrrolidinehydrochloride

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Reagent Code: #237821
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CAS Number 1638744-40-7

science Other reagents with same CAS 1638744-40-7

blur_circular Chemical Specifications

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Weight 157.59 g/mol
Formula C₅H₁₀ClF₂N
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MDL Number MFCD28501341
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of enzyme inhibitors and receptor modulators due to the presence of the difluoromethyl group, which enhances metabolic stability and binding affinity. Commonly employed in the production of antidiabetic and antiviral agents, where chirality plays a critical role in drug efficacy. The hydrochloride salt form improves solubility and handling in aqueous reaction environments.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,830.00
inventory 250mg
10-20 days ฿20,450.00
inventory 1g
10-20 days ฿62,300.00

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(3S)-3-(Difluoromethyl)pyrrolidinehydrochloride
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of enzyme inhibitors and receptor modulators due to the presence of the difluoromethyl group, which enhances metabolic stability and binding affinity. Commonly employed in the production of antidiabetic and antiviral agents, where chirality plays a critical role in drug efficacy. The hydrochloride salt form improve

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structure supports the development of enzyme inhibitors and receptor modulators due to the presence of the difluoromethyl group, which enhances metabolic stability and binding affinity. Commonly employed in the production of antidiabetic and antiviral agents, where chirality plays a critical role in drug efficacy. The hydrochloride salt form improves solubility and handling in aqueous reaction environments.

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