The defined (5S) stereochemistry preserves the conformational preferences of the proline ring, which is critical for controlling backbone geometry in downstream synthesis. L-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S)- is a protected dipeptide derivative used as a synthetic intermediate in peptide and medicinal chemistry.It comprises an L-valine residue linked via an amide bond to 5-methyl-L-proline, with the N-terminus protected as a methoxycarbonyl (carbamate).
L-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S)
| API Name | Velpatasvir |
|---|---|
| CAS No | 1335316-40-9 |
| Molecular Formula | C13H22N2O5 |
| Molecular Weight | 286.32 g/mol |
| Synonyms | (2S,5S)-1-[(2S)-2-(methoxycarbonylamino)-3-methylbutanoyl]-5-methylpyrrolidine-2-carboxylic acid |
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Frequently Asked Questions
The defined (5S) stereochemistry preserves the conformational preferences of the proline ring, which is critical for controlling backbone geometry in downstream synthesis. L-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S)- is a protected dipeptide derivative used as a synthetic intermediate in peptide and medicinal chemistry.It comprises an L-valine residue linked via an amide bond to 5-methyl-L-proline, with the N-terminus protected as a methoxycarbonyl (carbamate).
The CAS number of L-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S) is 1335316-40-9.
The molecular formula of L-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S) is C13H22N2O5.
The listed molecular weight of L-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S) is 286.32 g/mol.
L-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S) is listed as being used in connection with the following API: Velpatasvir.
The listed synonym or IUPAC name for L-Proline, N-(methoxycarbonyl)-L-valyl-5-methyl-, (5S) is (2S,5S)-1-[(2S)-2-(methoxycarbonylamino)-3-methylbutanoyl]-5-methylpyrrolidine-2-carboxylic acid.