4-(2-Aminothiazol-4-yl)benzene-1,3-diol hydrochloride

95%

Reagent Code: #138586
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CAS Number 472979-20-7

science Other reagents with same CAS 472979-20-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.7 g/mol
Formula C₉H₉ClN₂O₂S
badge Registry Numbers
MDL Number MFCD01849140
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in pharmaceutical synthesis, particularly in the development of antibiotics and antimicrobial agents. It serves as a key intermediate in constructing beta-lactam antibiotic derivatives, enhancing their spectrum of activity. Its structure supports binding to bacterial cell wall targets, improving efficacy. Also explored in medicinal chemistry for designing kinase inhibitors and anti-inflammatory compounds due to its ability to interact with biological targets through hydrogen bonding and aromatic interactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿790.00
inventory 250mg
10-20 days ฿1,880.00

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4-(2-Aminothiazol-4-yl)benzene-1,3-diol hydrochloride
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Used in pharmaceutical synthesis, particularly in the development of antibiotics and antimicrobial agents. It serves as a key intermediate in constructing beta-lactam antibiotic derivatives, enhancing their spectrum of activity. Its structure supports binding to bacterial cell wall targets, improving efficacy. Also explored in medicinal chemistry for designing kinase inhibitors and anti-inflammatory compounds due to its ability to interact with biological targets through hydrogen bonding and aromatic int

Used in pharmaceutical synthesis, particularly in the development of antibiotics and antimicrobial agents. It serves as a key intermediate in constructing beta-lactam antibiotic derivatives, enhancing their spectrum of activity. Its structure supports binding to bacterial cell wall targets, improving efficacy. Also explored in medicinal chemistry for designing kinase inhibitors and anti-inflammatory compounds due to its ability to interact with biological targets through hydrogen bonding and aromatic interactions.

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