Ethyl (2-Amino-4-thiazolyl)acetate

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Reagent Code: #182951
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CAS Number 53266-94-7

science Other reagents with same CAS 53266-94-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.23 g/mol
Formula C₇H₁₀N₂O₂S
badge Registry Numbers
MDL Number MFCD00005330
thermostat Physical Properties
Melting Point 94°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Widely used in the pharmaceutical industry as a key intermediate in the synthesis of β-lactam antibiotics, particularly cephalosporins. Its structure supports the construction of the thiazole ring system, which is essential for the biological activity of these antibiotics. It is also employed in the preparation of other bioactive molecules and heterocyclic compounds due to its amine and ester functional groups, which allow for versatile chemical modifications. Commonly utilized in research settings for developing new antimicrobial agents and in process optimization for antibiotic manufacturing.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿340.00
inventory 100g
10-20 days ฿990.00
inventory 5g
10-20 days ฿162.00

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Ethyl (2-Amino-4-thiazolyl)acetate
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Widely used in the pharmaceutical industry as a key intermediate in the synthesis of β-lactam antibiotics, particularly cephalosporins. Its structure supports the construction of the thiazole ring system, which is essential for the biological activity of these antibiotics. It is also employed in the preparation of other bioactive molecules and heterocyclic compounds due to its amine and ester functional groups, which allow for versatile chemical modifications. Commonly utilized in research settings for d

Widely used in the pharmaceutical industry as a key intermediate in the synthesis of β-lactam antibiotics, particularly cephalosporins. Its structure supports the construction of the thiazole ring system, which is essential for the biological activity of these antibiotics. It is also employed in the preparation of other bioactive molecules and heterocyclic compounds due to its amine and ester functional groups, which allow for versatile chemical modifications. Commonly utilized in research settings for developing new antimicrobial agents and in process optimization for antibiotic manufacturing.

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