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1914-58-5,MFCD00002783
Catalog No.:AA002F4Z

1914-58-5 | Trans-styrylacetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$13.00   $9.00
- +
1g
95%
in stock  
$28.00   $20.00
- +
5g
98%
in stock  
$127.00   $89.00
- +
25g
98%
in stock  
$552.00   $387.00
- +
100g
≥ 99% (GC)
in stock  
$2,051.00   $1,436.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002F4Z
Chemical Name:
Trans-styrylacetic acid
CAS Number:
1914-58-5
Molecular Formula:
C10H10O2
Molecular Weight:
162.1852
MDL Number:
MFCD00002783
SMILES:
OC(=O)C/C=C/c1ccccc1
Properties
Properties
 
BP:
228.88°C (rough estimate)  
Form:
Solid  
MP:
84-86 °C(lit.)  
Refractive Index:
1.6000 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
167  
Covalently-Bonded Unit Count:
1  
Defined Bond Stereocenter Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
2.3  

Downstream Synthesis Route

[1]Yang,Shan;Liu,Lingling;Zhou,Zheng;Huang,Zhibin;Zhao,Yingsheng[OrganicLetters,2021,vol.23,#2,p.296-299]

Literature

Title: Fragrance material review on 4-phenyl-3-buten-2-ol.

Journal: Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20120901

Title: Synthesis and antimalarial and antituberculosis activities of a series of natural and unnatural 4-methoxy-6-styryl-pyran-2-ones, dihydro analogues and photo-dimers.

Journal: Bioorganic & medicinal chemistry 20120215

Title: p38 MAPK activation, JNK inhibition, neoplastic growth inhibition, and increased gap junction communication in human lung carcinoma and Ras-transformed cells by 4-phenyl-3-butenoic acid.

Journal: Journal of cellular biochemistry 20120101

Title: Enhanced neuropeptide Y synthesis during intermittent hypoxia in the rat adrenal medulla: role of reactive oxygen species-dependent alterations in precursor peptide processing.

Journal: Antioxidants & redox signaling 20110401

Title: Probing the peptidylglycine alpha-hydroxylating monooxygenase active site with novel 4-phenyl-3-butenoic acid based inhibitors.

Journal: ChemMedChem 20100903

Title: Anti-inflammatory effects of 4-phenyl-3-butenoic acid and 5-(acetylamino)-4-oxo-6-phenyl-2-hexenoic acid methyl ester, potential inhibitors of neuropeptide bioactivation.

Journal: The Journal of pharmacology and experimental therapeutics 20070301

Title: Study of polarized IR spectra of the hydrogen bond system in crystals of styrylacetic acid.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20061001

Title: Isolation and antifungal activity of 4-phenyl-3-butenoic acid from Streptomyces koyangensis strain VK-A60.

Journal: Journal of agricultural and food chemistry 20051005

Title: Streptomyces koyangensis sp. nov., a novel actinomycete that produces 4-phenyl-3-butenoic acid.

Journal: International journal of systematic and evolutionary microbiology 20050101

Title: Peptidyl-glycine alpha-amidating monooxygenase targeting and shaping of atrial secretory vesicles: inhibition by mutated N-terminal ProANP and PBA.

Journal: Circulation research 20041210

Title: Reversal of the transformed phenotype and inhibition of peptidylglycine alpha-monooxygenase in Ras-transformed cells by 4-phenyl-3-butenoic acid.

Journal: Molecular carcinogenesis 20041201

Title: Oleic acid derived metabolites in mouse neuroblastoma N18TG2 cells.

Journal: Biochemistry 20041005

Title: Glycine-extended adrenomedullin exerts vasodilator effect through amidation in the rat aorta.

Journal: Regulatory peptides 20030515

Title: Intracellular angiotensin II increases the long isoform of PDGF mRNA in rat hepatoma cells.

Journal: Journal of molecular and cellular cardiology 20021101

Title: The phenylacetyl-CoA catabolon: a complex catabolic unit with broad biotechnological applications.

Journal: Molecular microbiology 20010301

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