CAS 3397-33-9

1,2-Pyrrolidinedicarboxylic acid, 2-(2,5-dioxo-1-pyrrolidinyl) 1-(phenylmethyl) ester, (2S)-

Description:

1,2-Pyrrolidinedicarboxylic acid, 2-(2,5-dioxo-1-pyrrolidinyl) 1-(phenylmethyl) ester, (2S)-, is a chemical compound characterized by its complex structure, which includes a pyrrolidine ring and multiple carboxylic acid functional groups. This compound features a stereocenter, indicating chirality, which can influence its biological activity and interactions. It is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or other fine chemicals. The presence of the phenylmethyl group suggests potential applications in medicinal chemistry, as aromatic rings often enhance the lipophilicity and biological activity of compounds. Additionally, the dioxo functionality indicates potential reactivity, making it a candidate for further chemical transformations. Its CAS number, 3397-33-9, allows for easy identification in chemical databases and literature. Overall, this compound exemplifies the intricate relationship between structure and function in organic chemistry, with implications for various applications in research and industry.

Formula: C₁₇H₁₈N₂O₆

InChI: InChI=1S/C17H18N2O6/c20-14-8-9-15(21)19(14)25-16(22)13-7-4-10-18(13)17(23)24-11-12-5-2-1-3-6-12/h1-3,5-6,13H,4,7-11H2/t13-/m0/s1

InChI key: InChIKey=BDNYCEKWUBRCBJ-ZDUSSCGKSA-N

SMILES: C(ON1C(=O)CCC1=O)(=O)[C@H]2N(C(OCC3=CC=CC=C3)=O)CCC2

Synonyms:

• 1,2-Pyrrolidinedicarboxylic acid, 1-benzyl ester, succinimido deriv., <span class="text-smallcaps">L</span>-
• 1,2-Pyrrolidinedicarboxylic acid, 2-(2,5-dioxo-1-pyrrolidinyl) 1-(phenylmethyl) ester, (2S)-
• 1-O-Benzyl 2-O-(2,5-dioxopyrrolidin-1-yl) (2S)-pyrrolidine-1,2-dicarboxylate
• 1-Pyrrolidinecarboxylic acid, 2-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-, phenylmethyl ester, (2S)-
• 1-Pyrrolidinecarboxylic acid, 2-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-, phenylmethyl ester, (S)-
• 2,5-Dioxopyrrolidin-1-Yl 1-[(Benzyloxy)Carbonyl]Prolinate
• 2,5-dioxopyrrolidin-1-yl 1-[(benzyloxy)carbonyl]-L-prolinate
• <span class="text-smallcaps">L</span>-Proline, 1-pyrrolidinecarboxylic acid deriv.
• Benzyloxycarbonyl-<span class="text-smallcaps">L</span>-proline ester with N-hydroxysuccinimide
• N-cbz-L-proline N-hydroxysuccinimide*ester
• Succinimide, N-[(1-carboxy-<span class="text-smallcaps">L</span>-prolyl)oxy]-, benzyl ester
• Z-Pro-OSu
• 1,2-Pyrrolidinedicarboxylic acid, 1-benzyl ester, succinimido deriv., L-

Z-Pro-OSu

CAS: 3397-33-9

Bachem ID: 4000215.

Formula: C₁₇H₁₈N₂O₆

Purity: > 99%

Color and Shape: White

Molecular weight: 346.34

Ref: 01-4000215

Z-Pro-OSu

CAS: 3397-33-9

Formula: C₁₇H₁₈N₂O₆

Purity: 98%

Color and Shape: Solid

Molecular weight: 346.3346

Ref: IN-DA00BZTI

Z-Pro-OSu

CAS: 3397-33-9

Z-Pro-OSu

Purity: 98%

Molecular weight: 346.34g/mol

Ref: 54-OR1034445

Z-Pro-OSu

CAS: 3397-33-9

Formula: C₁₇H₁₈N₂O₆

Purity: 95%

Color and Shape: Solid

Molecular weight: 346.339

Ref: 10-F224403

Z-L-proline N-hydroxysuccinimide ester

CAS: 3397-33-9

Z-L-proline N-hydroxysuccinimide ester is an endopeptidase that hydrolyzes peptides at the carboxyl end of the alpha amino acid. It has been shown to be active against a wide range of peptides such as those derived from human skin and nature, as well as multistep polypeptides. The enzyme has been shown to be labile in acidic environments, with a residue of about 10%. Z-L-proline N-hydroxysuccinimide ester also inhibits the aminoglycoside antibiotics gentamicin and streptomycin, which are used in the treatment of bacterial infections.

Formula: C₁₇H₁₈N₂O₆

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 346.33 g/mol

Ref: 3D-FP47841