1-Benzyl-3-(Cbz-amino)-2,5-pyrrolidinedione - CAS 1219424-59-5
Catalog: |
BB005301 |
Product Name: |
1-Benzyl-3-(Cbz-amino)-2,5-pyrrolidinedione |
CAS: |
1219424-59-5 |
Synonyms: |
N-[2,5-dioxo-1-(phenylmethyl)-3-pyrrolidinyl]carbamic acid (phenylmethyl) ester; benzyl N-(1-benzyl-2,5-dioxopyrrolidin-3-yl)carbamate |
IUPAC Name: | benzyl N-(1-benzyl-2,5-dioxopyrrolidin-3-yl)carbamate |
Description: | 1-Benzyl-3-(Cbz-amino)-2,5-pyrrolidinedione (CAS# 1219424-59-5) is a useful research chemical. |
Molecular Weight: | 338.36 |
Molecular Formula: | C19H18N2O4 |
Canonical SMILES: | C1C(C(=O)N(C1=O)CC2=CC=CC=C2)NC(=O)OCC3=CC=CC=C3 |
InChI: | InChI=1S/C19H18N2O4/c22-17-11-16(18(23)21(17)12-14-7-3-1-4-8-14)20-19(24)25-13-15-9-5-2-6-10-15/h1-10,16H,11-13H2,(H,20,24) |
InChI Key: | DRPFKGKSRKPPCG-UHFFFAOYSA-N |
Storage: | Sealed in dry, Room Temperature |
LogP: | 2.38280 |
Publication Number | Title | Priority Date |
US-6348600-B1 | Methods for making optically active 3-aminopyrrolidine-2,5-dione derivative and optically active 3-aminopyrrolidine derivative | 20010220 |
JP-2002316977-A | Method for producing optically active 1H-3-aminopyrrolidine compound | 20000824 |
EP-1311518-A1 | Preparation of n-protected-3-pyrrolidine-lactam substituted phosphonium salts | 20000814 |
EP-1311518-B1 | Preparation of n-protected-3-pyrrolidine-lactam substituted phosphonium salts | 20000814 |
US-2003195364-A1 | Preparation of n-protected-3-pyrrolidine-lactam substituted phosphonium salts | 20000814 |
Complexity: | 496 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 338.12665706 |
Formal Charge: | 0 |
Heavy Atom Count: | 25 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 338.12665706 |
Rotatable Bond Count: | 6 |
Topological Polar Surface Area: | 75.7 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 2 |
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