2-(Dimethylamino)acetohydrazide hydrochloride

≥95%

Reagent Code: #179509
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CAS Number 539-64-0

science Other reagents with same CAS 539-64-0

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Weight 153.61 g/mol
Formula C₄H₁₂ClN₃O
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MDL Number MFCD00042020
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of hydrazide-based drugs with potential antimicrobial and antitubercular activity. It serves as a building block in the preparation of heterocyclic compounds such as 1,3,4-oxadiazoles and 1,2,4-triazoles, which are common scaffolds in medicinal chemistry. Also employed in the design of enzyme inhibitors and bioactive molecules due to its ability to form stable derivatives with carbonyl compounds. Its hydrazide functionality allows for easy modification and conjugation, making it valuable in drug discovery and development processes.

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inventory 5g
10-20 days ฿32,190.00

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2-(Dimethylamino)acetohydrazide hydrochloride
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of hydrazide-based drugs with potential antimicrobial and antitubercular activity. It serves as a building block in the preparation of heterocyclic compounds such as 1,3,4-oxadiazoles and 1,2,4-triazoles, which are common scaffolds in medicinal chemistry. Also employed in the design of enzyme inhibitors and bioactive molecules due to its ability to form stable derivatives with carbonyl compounds. Its hyd

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of hydrazide-based drugs with potential antimicrobial and antitubercular activity. It serves as a building block in the preparation of heterocyclic compounds such as 1,3,4-oxadiazoles and 1,2,4-triazoles, which are common scaffolds in medicinal chemistry. Also employed in the design of enzyme inhibitors and bioactive molecules due to its ability to form stable derivatives with carbonyl compounds. Its hydrazide functionality allows for easy modification and conjugation, making it valuable in drug discovery and development processes.

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