L-Phenylglycine

Product Details

CAS No:2935-35-5

MF:C8H9NO2

Appearance:white or off-white crystalline powder

Specification:99.0%

UN number:-

Package:1/5/10/25kgs/drum

Supply Capacity:Tons

Synonyms:H-(PHENYL)GLY-OH;H-L-PHG-OH;(+)-L-ALPHA-PHENYLGLYCINE;L-(+)-ALPHA-PHENYLGLYCINE;L(+)-ALPHA-AMINOPHENYLACETIC ACID;L-ALPHA-AMINOPHENYLACETIC ACID;L-AMINOPHENYLACETIC ACID;L-(+)-2-PHENYLGLYCINE; L-Phenylglycine; 2935-35-5; L-(+)-2-Phenylglycine; Phenylglycine, L-; Glycine, 2-phenyl-, L-; L-(+)-alpha-Aminophenylacetic acid; 3I753R0XI6; Benzeneacetic acid, alpha-amino-, (alphaS)-; DTXSID801022916; NSC-206293; Benzeneacetic acid, alpha-amino-, (S)-; L-Phg amino acid; RefChem:861740; 2-phenylglycine, (L)-; DTXCID901507343; 220-909-8; H-Phg-Oh; (S)-2-Amino-2-phenylacetic acid; (2S)-2-amino-2-phenylacetic acid; L-2-Phenylglycine; L-(+)-alpha-Phenylglycine; (S)-phenylglycine; L-(+)-|A-Phenylglycine; (2S)-amino(phenyl)acetic acid; MFCD00064403; L(+)-alpha-Phenylglycine; (S)-(+)-2-Phenylglycine; (2S)-2-ammonio-2-phenylacetate; (2S)-2-Amino-2-phenyl-acetic acid; (alphaS)-alpha-aminobenzeneacetic acid; L-alpha-Phenylglycine; CHEMBL378605; (2S)-amino(phenyl)ethanoic acid; M03226; NSC 206293; Benzeneacetic acid, .alpha.-amino-, (S)-; Benzeneacetic acid, .alpha.-amino-, (.alpha.S)-; (+)-PHENYLGLYCINE; UNII-3I753R0XI6; EINECS 220-909-8; (S)-AMINO(PHENYL)ACETIC ACID; (S)-(+)-alpha-Aminophenylacetic Acid; L-(+)-a-Phenylglycine; (s)-(+)-phenylglycine; L(+)-|_-Phenylglycine; L?(+)-|A-Phenylglycine; SCHEMBL71958; (S)-2-PHENYLGLYCINE; L-(+)-PHENYLGLYCINE; SCHEMBL6768591; S-(+)-a-Aminophenylacetic acid; CHEBI:439819; L-(+)-alpha-Phenylglycine, 99%; L(+)-.ALPHA.-PHENYLGLYCINE; .ALPHA.-PHENYLGLYCINE S-FORM; BDBM50179721; EBC-03396; MSK165325; (S)-AMINO-PHENYL-ACETIC ACID; AKOS015923207; S-(+)-.ALPHA.-PHENYLGLYCINE; CS-W018122; H-Phg-OH (S)-(+)-2-Phenylglycine; HY-W017406; L-.ALPHA.-AMINOPHENYLACETIC ACID; AC-10440; AS-14724; BP-12540; H-Phg-OH(Discontinued,SeeCPTD788391); SY005672; .ALPHA.-PHENYLGLYCINE S-FORM [MI]; (S)-.ALPHA.-AMINOBENZENEACETIC ACID; P1288; (S)-2-AMINO-2-(PHENYL)ETHANOIC ACID; EN300-60938; C18623; Q27225746; L-(+)-alpha-Phenylglycine, puriss., >=99.0% (NT); Z957336528

Product application:L-Phenylglycine,2935-35-5,(S)-alpha-Aminobenzeneacetic acid,(S)-(+)-2-Phenylglycine,L-alpha-Phenylglycine,Chiral unnatural amino acid,Chiral amino acid derivative,Beta-lactam antibiotic side chain,Cephalosporin synthesis intermediate,Penicillin side chain building block,Peptidomimetic building block,Chiral resolution agent,Chiral ligand precursor,Chiral agrochemical intermediate,Pharmaceutical intermediate CAS 2935-35-5,Fine organic synthesis raw material,High chiral purity L-phenylglycine 99%,Research biochemical,Custom synthesis intermediate,L-Phenylglycine manufacturer China,CAS 2935-35-5 supplier,Suzhou Health Chemicals amino acids,L-Phenylglycine wholesale bulk export

 

L-Phenylglycine serves as an indispensable, high-purity chiral building block and foundational unnatural amino acid extensively utilized across the pharmaceutical, beta-lactam antibiotic synthesis, peptidomimetic engineering, asymmetric catalysis, and fine agrochemical sectors. In the commercial manufacturing of active pharmaceutical ingredients (APIs), owing to its well-defined (S)-enantiomeric configuration and versatile functional groups, it functions as a critical side-chain intermediate for the semi-synthesis of major cephalosporin and penicillin antibiotics, as well as novel broad-spectrum antibacterial compounds. In medicinal chemistry and peptide drug discovery, the incorporation of this alpha-phenyl-substituted glycine core into peptidomimetic sequences modulates backbone conformational rigidity and shields adjacent peptide bonds from enzymatic cleavage, thereby significantly enhancing the metabolic half-life and cellular membrane permeability of therapeutic oncology and antiviral leads. In asymmetric synthesis and catalytic engineering, L-Phenylglycine is widely employed as a chiral template and chiral pool starting material to construct chiral oxazoline ligands, amino alcohol catalysts, and optical resolving agents for enantioselective transformation reactions. In specialized crop protection chemistry, it is utilized to synthesize structurally advanced chiral fungicides and selective herbicides. Furthermore, in academic and industrial laboratory research, L-Phenylglycine remains a classic biochemical standard for developing chiral chromatography stationary phases and studying amino acid stereoselective recognition kinetics.