3-(1H-Benzo[d]imidazol-1-yl)propanoic acid

98%

Reagent Code: #195577
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CAS Number 14840-18-7

science Other reagents with same CAS 14840-18-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.20 g/mol
Formula C₁₀H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD00817167
thermostat Physical Properties
Boiling Point 415.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of drugs targeting enzyme inhibition and receptor modulation. Its structure supports conjugation in peptide-like molecules, making it valuable in designing enzyme inhibitors and antimicrobial agents. Also explored in the synthesis of fluorescent probes due to the benzimidazole moiety’s photophysical properties. Commonly employed in medicinal chemistry for modifying drug candidates to improve solubility and binding affinity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿159.50
1g
10-20 days ฿750.00
3-(1H-Benzo[d]imidazol-1-yl)propanoic acid
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Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of drugs targeting enzyme inhibition and receptor modulation. Its structure supports conjugation in peptide-like molecules, making it valuable in designing enzyme inhibitors and antimicrobial agents. Also explored in the synthesis of fluorescent probes due to the benzimidazole moiety’s photophysical properties. Commonly employed in medicinal chemistry for modifying drug candidates to i

Used in pharmaceutical research as an intermediate for synthesizing bioactive compounds, particularly in the development of drugs targeting enzyme inhibition and receptor modulation. Its structure supports conjugation in peptide-like molecules, making it valuable in designing enzyme inhibitors and antimicrobial agents. Also explored in the synthesis of fluorescent probes due to the benzimidazole moiety’s photophysical properties. Commonly employed in medicinal chemistry for modifying drug candidates to improve solubility and binding affinity.

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