2-Amino-2-(2,6-difluorophenyl)ethanol hydrochloride

95%

Reagent Code: #138248
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CAS Number 1311317-35-7

science Other reagents with same CAS 1311317-35-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.62 g/mol
Formula C₈H₁₀ClF₂NO
badge Registry Numbers
MDL Number MFCD18917323
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used in the synthesis of fluorinated pharmaceutical intermediates, particularly in the development of antifungal agents. Featuring an amino and hydroxymethyl group on a stereogenic carbon with a 2,6-difluorophenyl substituent, its structure supports the creation of chiral building blocks for bioactive molecules. Commonly employed in medicinal chemistry for optimizing drug potency and metabolic stability. Also utilized in asymmetric synthesis due to its stereogenic center, enabling the production of enantiomerically pure compounds.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,820.00
250mg
10-20 days ฿17,330.00
1g
10-20 days ฿55,910.00
2-Amino-2-(2,6-difluorophenyl)ethanol hydrochloride
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Used in the synthesis of fluorinated pharmaceutical intermediates, particularly in the development of antifungal agents. Featuring an amino and hydroxymethyl group on a stereogenic carbon with a 2,6-difluorophenyl substituent, its structure supports the creation of chiral building blocks for bioactive molecules. Commonly employed in medicinal chemistry for optimizing drug potency and metabolic stability. Also utilized in asymmetric synthesis due to its stereogenic center, enabling the production of enant

Used in the synthesis of fluorinated pharmaceutical intermediates, particularly in the development of antifungal agents. Featuring an amino and hydroxymethyl group on a stereogenic carbon with a 2,6-difluorophenyl substituent, its structure supports the creation of chiral building blocks for bioactive molecules. Commonly employed in medicinal chemistry for optimizing drug potency and metabolic stability. Also utilized in asymmetric synthesis due to its stereogenic center, enabling the production of enantiomerically pure compounds.

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