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75857-94-2

  • Product Name1-Benzyl 2-methyl (2S)-5-oxo-1,2-pyrrolidinedicarboxylate, Cbz-Pyr-Ome
  • Molecular FormulaC14H15NO5
  • Molecular Weight277.277
  • Purity99%
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Product Details

Quick Details

  • CasNo: 75857-94-2
  • Molecular Formula: C14H15NO5
  • Purity: 99%

High Quality 1-Benzyl 2-methyl (2S)-5-oxo-1,2-pyrrolidinedicarboxylate 75857-94-2 (Cbz-Pyr-Ome)

  • Molecular Formula:C14H15NO5
  • Molecular Weight:277.277
  • Boiling Point:452.3±45.0 °C(Predicted) 
  • PSA:72.91000 
  • Density:1.306±0.06 g/cm3(Predicted) 
  • LogP:1.42510 

1-Benzyl 2-methyl (2S)-5-oxo-1,2-pyrrolidinedicarboxylate(Cas 75857-94-2) Usage

Chemical Properties

white crystals or fine crystalline powder

Uses

1-Benzyl 2-methyl (2S)-5-oxo-1,2-pyrrolidinedicarboxylate is a derivative of pyrrole and has been synthesized using various methods.

General Description

1-Benzyl 2-methyl (2S)-5-oxo-1,2-pyrrolidinedicarboxylate is a usefull chemical material. The chemical formula of  1,2-Pyrrolidinedicarboxylic acid, 5-oxo-, 2-methyl 1-(phenylmethyl) ester, (S)- is C14H15NO5 which containing 14 Carbon atoms,15 Hydrogen atoms,1 Nitrogen atoms and 5 Oxygen atoms,and the molecular weight of  1,2-Pyrrolidinedicarboxylic acid, 5-oxo-, 2-methyl 1-(phenylmethyl) ester, (S)- is 277.277.

Isomeric SMILES: COC(=O)[C@@H]1CCC(=O)N1C(=O)OCC2=CC=CC=C2  
InChIKey: MBOBZGBHABMDMC-NSHDSACASA-N  
InChI: InChI=1S/C14H15NO5/c1-19-13(17)11-7-8-12(16)15(11)14(18)20-9-10-5-3-2-4-6-10/h2-6,11H,7-9H2,1H3/t11-/m0/s1  

Cbz-Pyr-Ome 75857-94-2 Relevant articles

Synthesis of highly functionalized 2,5-disubstituted pyrrolidines via an aza-Morita-Baylis-Hillman-type reaction

Kitulagoda, James E.,Palmelund, Anders,Aggarwal, Varinder K.

supporting information; experimental part, p. 6293 - 6299 (2010/10/19)

An aza-Morita-Baylis-Hillman-type reacti...

Scale-up of trisodium [(3Β,5Β,12α)-3-[[4(S)-4-[bis[2- [bis[(carboxy-kO)methyl]aminokN] ethyl]amino-kN]-4-(carboxy-kO)-1-oxobutyl] amino]-12-hydroxycholan-24- oato(6-)]gadolinate(3-)], a Gd(III) complex under development as a contrast agent for MRI coronary angiography

Anelli, Pier Lucio,Brocchetta, Marino,Lattuada, Luciano,Manfredi, Giuseppe,Morosini, Pierfrancesco,Murru, Marcella,Palano, Daniela,Sipioni, Marco,Visigalli, Massimo

scheme or table, p. 739 - 746 (2010/04/22)

Process chemistry involved in the discov...

Synthesis, determination of the absolute stereochemistry, and evaluations at the nicotinic acetylcholine receptors of a hydroxyindolizidine alkaloid from the ant Myrmicaria melanogaster

Zhou, Dejun,Toyooka, Naoki,Nemoto, Hideo,Yamaguchi, Kaoru,Tsuneki, Hiroshi,Wada, Tsutomu,Sasaoka, Toshiyasu,Sakai, Hideki,Tezuka, Yasuhiro,Kadota, Shigetoshi,Jones, Tappey H.,Garraffo, H. Martin,Spande, Thomas F.,Daly, John W.

experimental part, p. 565 - 571 (2009/12/05)

The first chiral synthesis of new hydrox...

Blood pool agents for nuclear magnetic resonance diagnostics

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Page/Page column 17; 27; 51, (2008/12/06)

The present invention relates to bile ac...

75857-94-2 Process route

Cbz-L-pGlu-OH
32159-21-0

Cbz-L-pGlu-OH

methyl iodide
74-88-4

methyl iodide

(5S)-N-(benzyloxycarbonyl)-5-methoxycarbonyl-2-pyrrolidinone
75857-94-2

(5S)-N-(benzyloxycarbonyl)-5-methoxycarbonyl-2-pyrrolidinone

Conditions
Conditions Yield
With N-ethyl-N,N-diisopropylamine; In dichloromethane;
98%
With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 6.5h; Heating / reflux;
98%
dibenzyl dicarbonate
31139-36-3

dibenzyl dicarbonate

methyl (S)-pyroglutamate
4931-66-2

methyl (S)-pyroglutamate

(5S)-N-(benzyloxycarbonyl)-5-methoxycarbonyl-2-pyrrolidinone
75857-94-2

(5S)-N-(benzyloxycarbonyl)-5-methoxycarbonyl-2-pyrrolidinone

Conditions
Conditions Yield
With dmap; In acetonitrile; at 20 ℃; for 3h;
75%

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