8-Chloro-1,2,3,4-tetrahydroquinoline

95%

Reagent Code: #163464
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CAS Number 90562-36-0

science Other reagents with same CAS 90562-36-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.64 g/mol
Formula C₉H₁₀ClN
badge Registry Numbers
MDL Number MFCD09034968
inventory_2 Storage & Handling
Storage Store at room temperature away from light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antipsychotic drugs. It serves as a building block in medicinal chemistry due to its structural similarity to bioactive quinoline and tetrahydroquinoline derivatives. Its chloro-substituted ring enhances reactivity for further functionalization, enabling the creation of more complex molecules for drug discovery. Also explored in the design of selective enzyme inhibitors and receptor ligands.

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Test Parameter Specification
Appearance Light Yellow to Brown Liquid
Purity 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,440.00
inventory 1g
10-20 days ฿13,350.00
inventory 250mg
10-20 days ฿3,680.00

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8-Chloro-1,2,3,4-tetrahydroquinoline
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antipsychotic drugs. It serves as a building block in medicinal chemistry due to its structural similarity to bioactive quinoline and tetrahydroquinoline derivatives. Its chloro-substituted ring enhances reactivity for further functionalization, enabling the creation of more complex molecules for drug discovery. Also explored in the design of selective enzyme inhibitors and re

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antipsychotic drugs. It serves as a building block in medicinal chemistry due to its structural similarity to bioactive quinoline and tetrahydroquinoline derivatives. Its chloro-substituted ring enhances reactivity for further functionalization, enabling the creation of more complex molecules for drug discovery. Also explored in the design of selective enzyme inhibitors and receptor ligands.

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