(2-Aminothiazol-5-yl)methanol

97%

Reagent Code: #136958
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CAS Number 131184-73-1

science Other reagents with same CAS 131184-73-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.17 g/mol
Formula C₄H₆N₂OS
badge Registry Numbers
MDL Number MFCD06203018
thermostat Physical Properties
Boiling Point 340.738°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly antibiotics and antiviral agents. Its structure is commonly incorporated into beta-lactamase inhibitors and cephalosporin-class drugs. Also serves as a building block in the development of biologically active heterocyclic compounds. Widely utilized in medicinal chemistry for designing new drug candidates due to its favorable reactivity and ability to bind with biological targets.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,230.00
inventory 250mg
10-20 days ฿2,030.00
inventory 1g
10-20 days ฿4,720.00
inventory 5g
10-20 days ฿21,800.00
(2-Aminothiazol-5-yl)methanol
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Used as a key intermediate in the synthesis of various pharmaceuticals, particularly antibiotics and antiviral agents. Its structure is commonly incorporated into beta-lactamase inhibitors and cephalosporin-class drugs. Also serves as a building block in the development of biologically active heterocyclic compounds. Widely utilized in medicinal chemistry for designing new drug candidates due to its favorable reactivity and ability to bind with biological targets.

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly antibiotics and antiviral agents. Its structure is commonly incorporated into beta-lactamase inhibitors and cephalosporin-class drugs. Also serves as a building block in the development of biologically active heterocyclic compounds. Widely utilized in medicinal chemistry for designing new drug candidates due to its favorable reactivity and ability to bind with biological targets.

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