1-N-Boc-2-Methylhydrazine
97%
- Product Code: 80187
CAS:
127799-54-6
| Molecular Weight: | 146.19 g./mol | Molecular Formula: | C₆H₁₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 49-51℃ | Boiling Point: | |
| Density: | 0.982±0.06 g/cm3 (20 ºC 760 Torr) | Storage Condition: | 2~8 ℃ |
Product Description:
1-N-Boc-2-Methylhydrazine is primarily used in organic synthesis as a protecting group for hydrazine derivatives. It is particularly valuable in the preparation of complex molecules, such as pharmaceuticals and agrochemicals, where selective protection and deprotection of functional groups are required. The Boc group (tert-butoxycarbonyl) provides stability to the hydrazine moiety during reactions, allowing for controlled transformations without unwanted side reactions. This compound is also employed in the synthesis of heterocycles and as a building block in the development of bioactive compounds. Its application extends to peptide chemistry, where it aids in the modification and functionalization of peptide chains.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97 100% |
| MP | 49 51? |
| APPEARANCE | SOLID |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿780.00 |
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| 1.000 | 10-20 days | ฿2,480.00 |
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| 5.000 | 10-20 days | ฿11,580.00 |
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1-N-Boc-2-Methylhydrazine
1-N-Boc-2-Methylhydrazine is primarily used in organic synthesis as a protecting group for hydrazine derivatives. It is particularly valuable in the preparation of complex molecules, such as pharmaceuticals and agrochemicals, where selective protection and deprotection of functional groups are required. The Boc group (tert-butoxycarbonyl) provides stability to the hydrazine moiety during reactions, allowing for controlled transformations without unwanted side reactions. This compound is also employed in the synthesis of heterocycles and as a building block in the development of bioactive compounds. Its application extends to peptide chemistry, where it aids in the modification and functionalization of peptide chains.
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