2-chloroacetohydrazide hydrochloride (1:1)
97%
- Product Code: 80435
CAS:
868-83-7
| Molecular Weight: | 144.9878 g./mol | Molecular Formula: | C₂H₆Cl₂N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01961484 | |
| Melting Point: | Boiling Point: | 316.3 °C at 760 mmHg | |
| Density: | Storage Condition: | room temperature |
Product Description:
2-Chloroacetohydrazide hydrochloride (1:1) is primarily utilized in organic synthesis as a key intermediate for the preparation of various hydrazide derivatives. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of antitubercular and antimicrobial agents. The compound’s reactive chloro and hydrazide groups make it suitable for constructing complex molecular structures. Additionally, it is used in the synthesis of heterocyclic compounds, which have applications in medicinal chemistry and drug discovery. Its role in facilitating the formation of hydrazone linkages also makes it valuable in the design of bioactive molecules and chemical probes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off-white powder |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,120.00 |
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| 1.000 | 10-20 days | ฿12,360.00 |
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2-chloroacetohydrazide hydrochloride (1:1)
2-Chloroacetohydrazide hydrochloride (1:1) is primarily utilized in organic synthesis as a key intermediate for the preparation of various hydrazide derivatives. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of antitubercular and antimicrobial agents. The compound’s reactive chloro and hydrazide groups make it suitable for constructing complex molecular structures. Additionally, it is used in the synthesis of heterocyclic compounds, which have applications in medicinal chemistry and drug discovery. Its role in facilitating the formation of hydrazone linkages also makes it valuable in the design of bioactive molecules and chemical probes.
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