155322

trans-Styrylacetic acid

96%

• Sinónimos: 4-Phenyl-3-butenoic acid
• Fórmula lineal: C₆H₅CH=CHCH₂CO₂H
• Número de CAS: 1914-58-5
• Peso molecular: 162.19
• MDL number: MFCD00002783
• UNSPSC Code: 12352100
• PubChem Substance ID: 24849516
• NACRES: NA.22

Propiedades

• Quality Level: 100
• assay: 96%
• greener alternative product score: old score: 22; new score: 3; Find out more about DOZN™ Scoring
• greener alternative product characteristics: Atom Economy; Design for Energy Efficiency; Use of Renewable Feedstocks; Learn more about the Principles of Green Chemistry.
• sustainability: Greener Alternative Product
• mp: 84-86 °C (lit.)
• functional group: carboxylic acid; phenyl
• greener alternative category: , Re-engineered
• SMILES string: OC(=O)C\C=C\c1ccccc1
• InChI: 1S/C10H10O2/c11-10(12)8-4-7-9-5-2-1-3-6-9/h1-7H,8H2,(H,11,12)/b7-4+
• InChI key: PSCXFXNEYIHJST-QPJJXVBHSA-N

Descripción

General description

The polarized IR spectra of the hydrogen bond system in trans-styrylacetic acid has been studied.

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Atom Economy”, “Design for Energy Efficiency” and “Use of Renewable Feedstock”. Click here to view its DOZN scorecard.

Application

trans-Styrylacetic acid (4-Phenyl-3-butenoic acid) was used as mechanism-based inhibitor of Peptidylglycine α-hydroxylating monooxygenase.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H315,H319,H335
• pcodes: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Hazard Classifications: Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• target_organs: Respiratory system
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Gloves