Name: Name:5-Phenylpentanoic acid
Brand: AABLOCKS
SKU: AA003MVO
Rating: 90 (10 reviews)

Technical Information

Catalog Number: AA003MVO

Chemical Name: 5-Phenylpentanoic acid

CAS Number: 2270-20-4

Molecular Formula: C11H14O2

Molecular Weight: 178.2277

MDL Number: MFCD00009109

SMILES: OC(=O)CCCCc1ccccc1

NSC Number: 65637

Properties

BP: 308.5±0.0°C at 760 mmHg

Form: Solid

MP: 58-60 °C(lit.);

Refractive Index: 1.4920 (estimate)

Storage: Keep in dry area;Room Temperature;

Complexity: 148

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 13

Hydrogen Bond Acceptor Count: 2

Hydrogen Bond Donor Count: 1

Isotope Atom Count: 0

Rotatable Bond Count: 5

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: 2.7

Literature fold

Title: Protective effects of 4-phenylbutyrate derivatives on the neuronal cell death and endoplasmic reticulum stress.

Journal: Biological & pharmaceutical bulletin20120101

Title: Activation of the plant mitochondrial potassium channel by free fatty acids and acyl-CoA esters: a possible defence mechanism in the response to hyperosmotic stress.

Journal: Journal of experimental botany20110101

Title: Specificity of procaine and ester hydrolysis by human, minipig, and rat skin and liver.

Journal: Drug metabolism and disposition: the biological fate of chemicals20071101

Title: Inter-individual variability in esterases in human liver.

Journal: Biochemical pharmacology20070915

Title: 4-Phenylbutyrate restores the functionality of a misfolded mutant low-density lipoprotein receptor.

Journal: The FEBS journal20070401

Title: Structure and polymer form of poly-3-hydroxyalkanoates produced by Pseudomonas oleovorans grown with mixture of sodium octanoate/undecylenic acid and sodium octanoate/5-phenylvaleric acid.

Journal: International journal of biological macromolecules20070130

Title: Effects of chromophore orientation and molecule conformation on surface-enhanced Raman scattering studied with alkanoic acids and colloidal silver nanoparticles.

Journal: The Journal of chemical physics20061221

Title: Induction and quantification of phenylacyl-CoA ligase enzyme activities in Pseudomonas putida CA-3 grown on aromatic carboxylic acids.

Journal: FEMS microbiology letters20051015

Title: Molecular characterization of extracellular medium-chain-length poly(3-hydroxyalkanoate) depolymerase genes from Pseudomonas alcaligenes strains.

Journal: Journal of microbiology (Seoul, Korea)20050601

Title: The inhibition of the high sensitive peripheral nerve soluble esterases by mipafox. A new mathematical processing for the kinetics of inhibition of esterases by organophosphorus compounds.

Journal: Toxicology letters20040615

Title: Metabolism of dietary procyanidins in rats.

Journal: Free radical biology & medicine20031015

Title: Properties of phenyl valerate esterase activities from chicken serum are comparable with soluble esterases of peripheral nerves in relation with organophosphorus compounds inhibition.

Journal: Toxicology letters20030430

Title: Intracellular degradation of two structurally different polyhydroxyalkanoic acids accumulated in Pseudomonas putida and Pseudomonas citronellolis from mixtures of octanoic acid and 5-phenylvaleric acid.

Journal: International journal of biological macromolecules20011210

Title: Paraoxon sensitive phenylvalerate hydrolase in assessing the severity of acute paraoxon poisoning.

Journal: Journal of toxicology. Clinical toxicology20010101

2270-20-4 | 5-Phenylpentanoic acid