(R)-1-(4-Chloro-2-fluorophenyl)ethan-1-amine hydrochloride

95%

Reagent Code: #230842
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CAS Number 856562-91-9

science Other reagents with same CAS 856562-91-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.08 g/mol
Formula C₈H₁₀Cl₂FN
badge Registry Numbers
MDL Number MFCD24414699
inventory_2 Storage & Handling
Storage Room temperature, inert gas storage

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the creation of fluorinated and chlorinated aromatic compounds, which are common motifs in modern drug design for enhancing metabolic stability and binding affinity. Commonly employed in the production of central nervous system agents and anti-inflammatory drugs. Also utilized in research settings for asymmetric synthesis and development of novel bioactive molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,430.00
250mg
10-20 days ฿11,120.00
1g
10-20 days ฿27,680.00
5g
10-20 days ฿64,030.00
(R)-1-(4-Chloro-2-fluorophenyl)ethan-1-amine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the creation of fluorinated and chlorinated aromatic compounds, which are common motifs in modern drug design for enhancing metabolic stability and binding affinity. Commonly employed in the production of central nervous system agents and anti-inflammatory drugs. Also utilized in research settings for as

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the creation of fluorinated and chlorinated aromatic compounds, which are common motifs in modern drug design for enhancing metabolic stability and binding affinity. Commonly employed in the production of central nervous system agents and anti-inflammatory drugs. Also utilized in research settings for asymmetric synthesis and development of novel bioactive molecules.

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