6-Chloro-2,3-dihydro-1H-pyrrolo[3,2-c]pyridine

≥95%

Reagent Code: #161966
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CAS Number 23596-25-0

science Other reagents with same CAS 23596-25-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.60 g/mol
Formula C₇H₇ClN₂
badge Registry Numbers
MDL Number MFCD00980787
thermostat Physical Properties
Boiling Point 287.2°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.291g/cm3
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, making it valuable in creating targeted therapies. Also employed in the preparation of neuroprotective compounds and investigational drugs for neurological disorders due to its ability to cross the blood-brain barrier. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and metabolic stability.

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Test Parameter Specification
Appearance White to yellow or pale-red or gray solid
Purity (%) 95-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,010.00
inventory 1g
10-20 days ฿11,770.00
inventory 250mg
10-20 days ฿4,896.00

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6-Chloro-2,3-dihydro-1H-pyrrolo[3,2-c]pyridine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, making it valuable in creating targeted therapies. Also employed in the preparation of neuroprotective compounds and investigational drugs for neurological disorders due to its ability to cross the blood-brain barrier. Commonly utilized in medicinal chemistry for scaffold modification to enhance dru

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, making it valuable in creating targeted therapies. Also employed in the preparation of neuroprotective compounds and investigational drugs for neurological disorders due to its ability to cross the blood-brain barrier. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and metabolic stability.

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