6-Chloroindolizine

95%

Reagent Code: #164014
fingerprint
CAS Number 1632285-97-2

science Other reagents with same CAS 1632285-97-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.59 g/mol
Formula C₈H₆ClN
badge Registry Numbers
MDL Number MFCD26143271
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in pharmaceutical research as a key scaffold for developing bioactive compounds, particularly in the design of kinase inhibitors and antimicrobial agents. Shows potential in studies related to anti-inflammatory and anticancer activities due to its ability to interact with cellular signaling pathways. Also employed in agrochemical research for developing novel pesticides with improved efficacy and selectivity. Its structural similarity to natural indole alkaloids makes it valuable in synthesizing derivatives for drug discovery and biological screening.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿28,220.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-Chloroindolizine
No image available

Used in pharmaceutical research as a key scaffold for developing bioactive compounds, particularly in the design of kinase inhibitors and antimicrobial agents. Shows potential in studies related to anti-inflammatory and anticancer activities due to its ability to interact with cellular signaling pathways. Also employed in agrochemical research for developing novel pesticides with improved efficacy and selectivity. Its structural similarity to natural indole alkaloids makes it valuable in synthesizing der

Used in pharmaceutical research as a key scaffold for developing bioactive compounds, particularly in the design of kinase inhibitors and antimicrobial agents. Shows potential in studies related to anti-inflammatory and anticancer activities due to its ability to interact with cellular signaling pathways. Also employed in agrochemical research for developing novel pesticides with improved efficacy and selectivity. Its structural similarity to natural indole alkaloids makes it valuable in synthesizing derivatives for drug discovery and biological screening.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...