4-(2-PIPERIDIN-1-YL-ETHOXY)-BENZOIC ACID HYDROCHLORIDE

98%

Reagent Code: #224855
label
Alias 4-(2-piperidinyl ethoxy)benzoic acid hydrochloride; 4-[2-piperidin-1-ethoxy]benzoic acid hydrochloride; 4-[2-(1-piperidinyl)ethoxy]benzoic acid hydrochloride; 4-[2-(1-piperidinyl)ethoxy]benzoic acid hydrochloride; 4-[2-(1-piperidinyl)ethoxy]benzoic acid hydrochloride
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CAS Number 84449-80-9

science Other reagents with same CAS 84449-80-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.77 g/mol
Formula C₁₄H₂₀ClNO₃
badge Registry Numbers
EC Number 282-882-9
MDL Number MFCD06657755
thermostat Physical Properties
Melting Point 267-271°C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in pharmaceutical research as an intermediate in the synthesis of selective estrogen receptor modulators (SERMs). It plays a key role in developing compounds for the treatment of hormone-dependent conditions such as breast cancer and osteoporosis. Its structure supports binding affinity to estrogen receptors with improved tissue selectivity. Also investigated for use in central nervous system agents due to its piperidine moiety, which can enhance blood-brain barrier penetration. Commonly employed in medicinal chemistry for optimizing drug candidates requiring carboxylic acid and basic amine functionalities.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿180.00
100g
10-20 days ฿2,652.00
25g
10-20 days ฿1,290.00
4-(2-PIPERIDIN-1-YL-ETHOXY)-BENZOIC ACID HYDROCHLORIDE
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Used in pharmaceutical research as an intermediate in the synthesis of selective estrogen receptor modulators (SERMs). It plays a key role in developing compounds for the treatment of hormone-dependent conditions such as breast cancer and osteoporosis. Its structure supports binding affinity to estrogen receptors with improved tissue selectivity. Also investigated for use in central nervous system agents due to its piperidine moiety, which can enhance blood-brain barrier penetration. Commonly employed in

Used in pharmaceutical research as an intermediate in the synthesis of selective estrogen receptor modulators (SERMs). It plays a key role in developing compounds for the treatment of hormone-dependent conditions such as breast cancer and osteoporosis. Its structure supports binding affinity to estrogen receptors with improved tissue selectivity. Also investigated for use in central nervous system agents due to its piperidine moiety, which can enhance blood-brain barrier penetration. Commonly employed in medicinal chemistry for optimizing drug candidates requiring carboxylic acid and basic amine functionalities.

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