Catalog No.:AA006LS5

67118-31-4 | 2-(2-Oxopyrrolidin-1-yl)butanoic acid

Name: Name:2-(2-Oxopyrrolidin-1-yl)butanoic acid
Brand: AABLOCKS
SKU: AA006LS5
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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA006LS5

Chemical Name:

2-(2-Oxopyrrolidin-1-yl)butanoic acid

CAS Number:

67118-31-4

Molecular Formula:

C8H13NO3

Molecular Weight:

171.1937

MDL Number:

MFCD08236692

SMILES:

CCC(N1CCCC1=O)C(=O)O

Properties

BP:

370.975°C at 760 mmHg

Form:

Solid

MP:

155-158 °C

Storage:

Keep in dry area;2-8℃;

Computed Properties

Complexity:

203

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

Undefined Atom Stereocenter Count:

XLogP3:

0.3

Downstream Synthesis Route

67118-31-4

102767-28-2

[1]TetrahedronAsymmetry,2005,vol.16,p.3739-3745

[2]TetrahedronAsymmetry,2005,vol.16,p.3739-3745

[3]Patent:CN110590635,2019,A

67118-31-4

102849-49-0

[1]Boschi,Francesca;Camps,Pelayo;Comes-Franchini,Mauro;Munoz-Torrero,Diego;Ricci,Alfredo;Sanchez,Laura[TetrahedronAsymmetry,2005,vol.16,#22,p.3739-3745]

[2]CurrentPatentAssignee:SHANDONGPOLYTECHNICCOLLEGE-CN110590635,2019,A

Literature

Title: Measurement of glycine binding site of N-methyl-D-asparate receptors in living human brain using 4-acetoxy derivative of L-703,717, 4-acetoxy-7-chloro-3-[3-(4-[11c] methoxybenzyl) phenyl]-2(1H)-quinolone (AcL703) with positron emission tomography.

Journal: Synapse (New York, N.Y.) 20071001

Title: A validated chiral LC method for the enantioselective analysis of Levetiracetam and its enantiomer R-alpha-ethyl-2-oxo-pyrrolidine acetamide on amylose-based stationary phase.

Journal: Journal of pharmaceutical and biomedical analysis 20040903

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