5-(1-(2-Chlorophenyl)-2-methoxy-2-oxoethyl)-6,7-dihydrothieno[3,2-c]pyridin-5-ium bromide

95%

Reagent Code: #157055
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CAS Number 2418591-12-3

science Other reagents with same CAS 2418591-12-3

blur_circular Chemical Specifications

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Weight 400.7 g/mol
Formula C₁₆H₁₅BrClNO₂S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of bioactive molecules. Its structural features, including the thienopyridinium core and chlorophenyl substituent, make it valuable in constructing complex heterocyclic systems with potential pharmacological activity. It is particularly employed in the design of enzyme inhibitors and receptor modulators due to its ability to interact with biological targets through ionic and π-π interactions. Additionally, its quaternary ammonium moiety enhances solubility and binding affinity, which is advantageous in medicinal chemistry for improving drug-like properties. The compound also finds use in studies involving fluorescent probes and as a building block in the synthesis of functionalized heterocycles for drug discovery.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿192,000.00

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5-(1-(2-Chlorophenyl)-2-methoxy-2-oxoethyl)-6,7-dihydrothieno[3,2-c]pyridin-5-ium bromide
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Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of bioactive molecules. Its structural features, including the thienopyridinium core and chlorophenyl substituent, make it valuable in constructing complex heterocyclic systems with potential pharmacological activity. It is particularly employed in the design of enzyme inhibitors and receptor modulators due to its ability to interact with biological targets through ionic and π-π

Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of bioactive molecules. Its structural features, including the thienopyridinium core and chlorophenyl substituent, make it valuable in constructing complex heterocyclic systems with potential pharmacological activity. It is particularly employed in the design of enzyme inhibitors and receptor modulators due to its ability to interact with biological targets through ionic and π-π interactions. Additionally, its quaternary ammonium moiety enhances solubility and binding affinity, which is advantageous in medicinal chemistry for improving drug-like properties. The compound also finds use in studies involving fluorescent probes and as a building block in the synthesis of functionalized heterocycles for drug discovery.

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