Indolizine-6-carboxylic acid

≥95%

Reagent Code: #200304
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CAS Number 588720-42-7

science Other reagents with same CAS 588720-42-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.16 g/mol
Formula C₉H₇NO₂
badge Registry Numbers
MDL Number MFCD10000610
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used in pharmaceutical research as a building block for synthesizing biologically active compounds. Its structure supports development of agents with potential antimicrobial, anti-inflammatory, and anticancer properties. Commonly employed in medicinal chemistry for designing drug candidates targeting neurological and oncological pathways. Also utilized in agrochemicals for developing novel pesticides due to its heterocyclic stability and reactivity. Serves as a scaffold in combinatorial chemistry for high-throughput screening of new therapeutic molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿21,320.00
250mg
10-20 days ฿42,650.00
Indolizine-6-carboxylic acid
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Used in pharmaceutical research as a building block for synthesizing biologically active compounds. Its structure supports development of agents with potential antimicrobial, anti-inflammatory, and anticancer properties. Commonly employed in medicinal chemistry for designing drug candidates targeting neurological and oncological pathways. Also utilized in agrochemicals for developing novel pesticides due to its heterocyclic stability and reactivity. Serves as a scaffold in combinatorial chemistry for high-t
Used in pharmaceutical research as a building block for synthesizing biologically active compounds. Its structure supports development of agents with potential antimicrobial, anti-inflammatory, and anticancer properties. Commonly employed in medicinal chemistry for designing drug candidates targeting neurological and oncological pathways. Also utilized in agrochemicals for developing novel pesticides due to its heterocyclic stability and reactivity. Serves as a scaffold in combinatorial chemistry for high-throughput screening of new therapeutic molecules.
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