AB50916
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 97% | in stock | $8.00 | $5.00 | - + | |
250mg | 97% | in stock | $15.00 | $10.00 | - + | |
1g | 97% | in stock | $16.00 | $12.00 | - + | |
5g | 97% | in stock | $23.00 | $17.00 | - + | |
10g | 97% | in stock | $46.00 | $33.00 | - + | |
25g | 97% | in stock | $113.00 | $80.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB50916 |
Chemical Name: | (S)-3-Aminobutan-1-ol |
CAS Number: | 61477-39-2 |
Molecular Formula: | C4H11NO |
Molecular Weight: | 89.1362 |
MDL Number: | MFCD08275763 |
SMILES: | C[C@@H](CCO)N |
Complexity: | 30.7 |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Heavy Atom Count: | 6 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 2 |
XLogP3: | -0.6 |
(S)-3-Aminobutan-1-ol, also known as (S)-3-aminobutanol, plays a crucial role in chemical synthesis as a chiral building block. Its unique stereochemistry allows for the creation of complex molecules with precise control over the arrangement of functional groups. In organic synthesis, (S)-3-Aminobutan-1-ol can be utilized as a chiral auxiliary in asymmetric synthesis reactions to induce stereocontrol and enhance enantioselectivity. It can serve as a key starting material for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Additionally, this compound can be employed in the synthesis of biologically active compounds, such as amino alcohols, amino acids, and peptides.By incorporating (S)-3-Aminobutan-1-ol into synthetic pathways, chemists can access a diverse array of structurally intricate molecules with specific stereochemical configurations. Its versatility and strategic importance make it a valuable tool in the synthesis of complex organic compounds with high levels of stereochemical purity.