AA09712
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 97% | in stock | $8.00 | $5.00 | - + | |
5g | 97% | in stock | $10.00 | $7.00 | - + | |
10g | 97% | in stock | $11.00 | $8.00 | - + | |
25g | 97% | in stock | $26.00 | $18.00 | - + | |
100g | 97% | in stock | $68.00 | $48.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA09712 |
Chemical Name: | N-Boc-2-amino-2-methyl-1-propanol |
CAS Number: | 102520-97-8 |
Molecular Formula: | C9H19NO3 |
Molecular Weight: | 189.2521 |
MDL Number: | MFCD03788641 |
SMILES: | OCC(NC(=O)OC(C)(C)C)(C)C |
Complexity: | 182 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 4 |
XLogP3: | 0.9 |
The tert-Butyl (1-hydroxy-2-methylpropan-2-yl)carbamate is a versatile compound that finds extensive application in chemical synthesis. As a carbamate derivative, this compound serves as a valuable protecting group in organic chemistry reactions. By selectively masking reactive functional groups, such as amines or alcohols, with the tert-butyl (1-hydroxy-2-methylpropan-2-yl)carbamate group, chemists can control the reactivity of these functional groups in multi-step organic synthesis processes. This protective group strategy enables chemists to carry out complex chemical transformations with enhanced selectivity and efficiency, facilitating the synthesis of various organic compounds with specific structural features and functionalities.