461393

(S)-β-Methylphenethylamine

99%

• Synonym(s): (S)-2-Phenyl-1-propylamine
• Linear Formula: C₆H₅CH(CH₃)CH₂NH₂
• CAS Number: 17596-79-1
• Molecular Weight: 135.21
• Beilstein/REAXYS Number: 3195645
• MDL number: MFCD00216741
• UNSPSC Code: 12352116
• PubChem Substance ID: 24869850
• NACRES: NA.22

Properties

• assay: 99%
• optical activity: [α]22/D −35°, c = 1 in ethanol
• refractive index: n20/D 1.525 (lit.)
• mp: 207 °C (lit.)
• density: 0.945 g/mL at 25 °C (lit.)
• SMILES string: C[C@H](CN)c1ccccc1
• InChI: 1S/C9H13N/c1-8(7-10)9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3/t8-/m1/s1
• InChI key: AXORVIZLPOGIRG-MRVPVSSYSA-N

Description

General description

Bacteriorhodopsin is the prototypical "seven-helix" transmembrane protein (with seven α-helical domains), whose study led to advances in understanding G protein-coupled receptors (GPCRs). In Halobacteria, it acts as a light-harvesting protein, producing a proton gradient across the cell wall that is then used to drive biosynthetic processes.

Application

Building block for the enantioselective synthesis of pyrizinostatin, a pyroglutamyl peptidase inhibitor.

Safety Information

• pictograms: GHS05
• signalword: Danger
• hcodes: H314
• pcodes: P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405
• Hazard Classifications: Skin Corr. 1B
• Storage Class: 8A - Combustible corrosive hazardous materials
• wgk_germany: WGK 3
• flash_point_f: 177.8 °F - closed cup
• flash_point_c: 81 °C - closed cup
• ppe: Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter