| Chemical Name: | Butanoic acid,4-[(2,2-dimethylpropoxy)sulfonyl]-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(2S)- |
| CAS Number: | 220951-81-5 |
| Product Number: | AG007PMK(AGN-PC-0QYOUL) |
| Synonyms: | |
| MDL No: | MFCD03424225 |
| Molecular Formula: | C24H29NO7S |
| Molecular Weight: | 475.5546 |
Fmoc-4-(neopentyloxysulfonyl)- L-aminobutyric acid is a valuable reagent commonly used in chemical synthesis, particularly in the field of peptide chemistry. This compound serves as a potent tool for solid-phase peptide synthesis due to its ability to protect and activate amino acids during the elongation of peptide chains.In peptide synthesis, Fmoc-4-(neopentyloxysulfonyl)- L-aminobutyric acid acts as a protecting group for the amino group of the amino acid residue. This protection prevents unintended reactions and ensures selective coupling of amino acids in the desired sequence. The Fmoc group is easily removed under mild conditions, allowing for efficient and high-yielding synthesis of peptides.Additionally, the neopentyloxysulfonyl moiety provides stability and compatibility with a variety of reaction conditions commonly encountered in peptide synthesis. This feature makes Fmoc-4-(neopentyloxysulfonyl)- L-aminobutyric acid a versatile building block for the preparation of complex peptides with tailored properties.Overall, the application of Fmoc-4-(neopentyloxysulfonyl)- L-aminobutyric acid in chemical synthesis offers chemists a reliable and efficient strategy for the assembly of peptide structures with precision and control.
![O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]](https://img.angenechemical.com/storage/3a59/3a5932eec850ab245f6f4d4a7f9497f9.png)
(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
O)CCS(=O)(=O)OCC(C)(C)C)OCC1c2ccccc2c2c1cccc2](https://img.angenechemical.com/storage/93e4/93e4f0a01284abd70865af8992084ed0.png)