2-Aminothiazol-4-acetic Acid丨CAS 29676-71-9

2-Aminothiazol-4-acetic Acid丨CAS 29676-71-9
Product Introduction:
Catalog No.: SS124934
CAS No.: 29676-71-9
Assay (on dried basis): 99% min
Product Name: 2-Aminothiazol-4-acetic acid
Certificate: ISO9001; ISO14001
Molecular Formula: C5H6N2O2S
Molecular Weight: 158.18
Synonym(s): (2-Aminothiazole-4-yl)acetic acid
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Technical Parameters
Description

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Specifications

 

Appearance White or off white powder
Assay (on dried basis) 99% min
Identification Conforms
Water 0.3% max
Melting point 129°C min
Individual impurity 1% max
Total impurities 1.5% max

 

Transport Information

 

Parameter

Specification

UN Number

 

Class

 

Packing Group

 

H.S. Code

2934999099305

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Keep container tightly closed. Store in a refrigerator.

Condition to Avoid

Heat. Exposure to air

Package

 

 

Manufacturing Information

 

Parameter

Specification

Capacity

10MT/month

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

Production since 1993

Stock

 

 

 

 

Applications

 

2-Aminothiazol-4-acetic acid (CAS 29676-71-9) is a heterocyclic amino acid derivative widely used as an intermediate in pharmaceutical and agrochemical synthesis. Its 2-aminothiazole core with an acetic acid side chain makes it a versatile building block for the design of β-lactam antibiotics, enzyme inhibitors, and other bioactive compounds. In medicinal chemistry, it is applied in the synthesis of penicillin and cephalosporin analogues, where the aminothiazole ring enhances antibacterial activity and binding specificity. In agrochemicals, it serves as a precursor for herbicides, fungicides, and insecticides with improved efficacy. Additionally, it is used in organic synthesis to create functionalized heterocycles and study structure–activity relationships in drug development.

 

Benefits

 

The benefits of 2-aminothiazol-4-acetic acid arise from its multifunctional reactivity and biologically relevant scaffold. The amino group allows selective derivatization, coupling, and condensation reactions, while the acetic acid moiety provides solubility and enables further functionalization. The aminothiazole ring contributes electronic and steric features that enhance binding affinity in biological targets. Its combination of reactivity, stability, and biological relevance makes it a highly adaptable intermediate for the efficient synthesis of antibiotics, agrochemicals, and other bioactive molecules.

 

Conclusion

 

In summary, 2-aminothiazol-4-acetic acid is a valuable heterocyclic intermediate in pharmaceutical and agrochemical synthesis. Its applications include the preparation of β-lactam antibiotics, enzyme inhibitors, and crop-protection agents, while its benefits lie in multifunctional reactivity, scaffold stability, and biological relevance. As demand for effective heterocyclic intermediates continues to grow, this compound remains a critical tool for designing and synthesizing bioactive molecules.

 

 

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