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Cat. No.: HY-W714837

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5-Phenyllevulinic acid

Name: 5-Phenyllevulinic acid
Brand: MedChemExpress
SKU: HY-W714837
Availability: PreOrder

(Synonyms: 4-Oxo-5-phenylpentanoic acid; 5-Phenyl-4-oxopentanoic acid)

5-Phenyllevulinic acid (4-Oxo-5-phenylpentanoic acid) is an endogenous fungal metabolite with inhibitory activity against the bacterium B. megaterium, the plant pathogenic fungus S. tritici, and the alga C. fusca. 5-Phenyllevulinic acid is also an intermediate in the synthesis of σ receptor ligands. 5-Phenyllevulinic acid holds potential for research in the field of anti-infection studies .

For research use only. We do not sell to patients.

CAS No.: 3183-15-1
Formula: C₁₁H₁₂O₃
Molecular Weight:192.21

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (265 KB)

5-Phenyllevulinic acid Chemical Structure

CAS No.: 3183-15-1

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity

Description

All Antibiotic Isoforms :

All Endogenous Metabolite Isoforms :

All Sigma Receptor Isoforms :

Chemical Information

CAS No. 3183-15-1
Molecular Weight 192.21
Formula C₁₁H₁₂O₃
SMILES

O=C(CC1=CC=CC=C1)CCC(O)=O
Synonyms

4-Oxo-5-phenylpentanoic acid; 5-Phenyl-4-oxopentanoic acid
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (265 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Lu S, et al. Bioactive aromatic derivatives from endophytic fungus, Cytospora sp. Nat Prod Commun. 2011 May;6(5):661-6. [Content Brief]

[2]. Ketterer C, et al. Lipase‐Catalyzed Kinetic Resolution of 2‐Phenylethanol Derivatives and Chiral Oxa‐Pictet–Spengler Reaction as the Key Steps in the Synthesis of Enantiomerically Pure Tricyclic Amines[J]. European Journal of Organic Chemistry, 2012, 2012(12): 2428-2444.

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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Biological Activity
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References

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5-Phenyllevulinic acid

All Antibiotic Isoforms

All Endogenous Metabolite Isoforms

All Sigma Receptor Isoforms