DL-alpha-Phenylglycine

Product Details

CAS No:2835-06-5

MF:C8H9NO2

Appearance:white or off-white crystalline powder

Specification:98.5%

UN number:-

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

Supply Capacity:Tons

Synonyms:(.+/-.)-alpha-Phenylglycine;(+/-)-benzeneaceticaci;.alpha.-amino-,(+-)-Benzeneaceticacid;-Aminobenzeneaceticacid;Benzeneacetic acid, alpha-amino-, (±Benzeneaceticacid,-amino-,(+-)-;PHENYLGLYCINE(D,L-),2-Phenylglycine,"2-Phenylglycine; 69-91-0; (+-)-ALPHA-PHENYLGLYCINE; 2-Amino-2-phenylacetic acid; 2835-06-5; H-DL-Phg-OH; DL-alpha-Phenylglycine; DL-Phenylglycine; DL-2-Phenylglycine; ALPHA-PHENYLGLYCINE; Amino(phenyl)acetic acid; Amino-phenyl-acetic acid; DL-a-phenylglycine; alpha-Aminophenylacetic acid; aminophenylacetic acid; DL-; A-Phenylglycine; Glycine, 2-phenyl-; MFCD00064402; Phenylglycine dl; alpha-Phenylgycine; alpha-Aminobenzeneacetic acid; 2-amino-2-phenyl-acetic acid; .alpha.-Aminobenzeneacetic acid; L-.alpha.-Phenylglycine; DL-.alpha.-Phenylglycine; 96S7ZZ1KHE; alpha-amino-alpha-Toluic acid; DL-PHENYL-D5-GLYCINE; CHEBI:55484; rac-2-amino-2-phenylacetic acid; DL-.alpha.-Aminophenylacetic acid; Benzeneacetic acid, .alpha.-amino-; NSC-7928; NSC-24619; NSC-32070; L-(+)-.alpha.-Aminophenylacetic acid; .alpha.-Phenylglycine; .alpha.-Aminophenylacetic acid; .alpha.-Toluic acid, .alpha.-amino-; (+/-)-alpha-Aminophenylacetic acid; DL-alpha-Aminophenylacetic acid; c-phenylglycine; Benzeneacetic acid, alpha-amino-; 2-phenyl-glycine; NSC 206293; amino(phenyl)acetate; Glycine, DL-; Benzeneacetic acid, .alpha.-amino-, (S)-; DL-2-phenyl-glycine; alpha-aminophenylacetate; (RS)-2-phenylglycine; DL-a-aminophenylacetate; alpha-aminobenzeneacetate; Benzeneacetic acid, .alpha.-amino-, (.alpha.S)-; 2-amino-2-phenylacetate; 2-Phenylglycine, 95%; alpha-amino-alpha-toluate; (+/-)-a-phenylglycine; alpha-amino-benzeneacetate; D(-)-alpha-Phenylglycine; L(+)-alpha-Phenylglycine; PHENYLGLYCINE, DL-; DL-alpha-aminophenylacetate; DL-alpha-phenylaminoacetate; UNII-96S7ZZ1KHE; Benzeneacetic acid, (S)-; DL-a-aminophenylacetic acid; (+/-)-alpha-phenylglycine; alpha-amino-benzeneacetic acid; SCHEMBL157180; DL-alpha-phenylaminoacetic acid; CHEMBL131226; orb1308891; SCHEMBL5164233; SCHEMBL5769768; SCHEMBL16670754; SCHEMBL27351647; SCHEMBL27397292; SCHEMBL27699174; (+/-)-a-Aminophenylacetic acid; (.+-.)-.alpha.-Phenylglycine; alpha-Toluic acid, alpha-amino-; DTXSID70862455; NSC7928; (.+/-.)-.alpha.-Phenylglycine; D(-)-alpha-Aminophenylacetic acid; Amino(phenyl)acetic acid-, (S)-; .ALPHA.-PHENYLGLYCINE [MI]; BCP30023; NSC 7928; NSC24619; NSC32070; EINECS 200-719-1; EINECS 220-608-1; BBL016492; NSC 24619; NSC 32070; NSC206293; SBB056598; STK182581; 2-AMINO-2-PHENYLETHANOIC ACID; AKOS000121220; AKOS016042338; (+/-)-.ALPHA.-PHENYLGLYCINE; AB00920; AB02597; CS-W010964; HY-W010248; 2-Phenylglycine; DL-alpha-Phenylglycine; CAS 69-91-0; DS-13892; SY006358; DB-047383; NS00077571; P0326; EN300-22835; A22760; D70539; DL-alpha-Phenylglycine, purum, 98.0% (NT); 2-Amino-2-phenylacetic acid; DL-2-Phenylglycine; Benzeneacetic acid, .alpha.-amino-, (.+/-.)-; SR-01000944793; SR-01000944793-1; Q15633805; 93378EBE-2D42-40BB-8CFB-2C976D8C188C; F2191-0177; Z147647142; Cephalexin Impurity A;D-(-)-alpha-Phenylglycine;H-D-PHG-OH; (R)-Phenylglycine;(R)-(-)-Alpha-aminophenylacetic acid;(R)-Alpha-aminophenylacetic acid",151.160,C8H9NO2,

Product application:DL-alpha-Phenylglycine, DL-a-Phenylglycine, DL-Phenylglycine, 2-Amino-2-phenylacetic acid, CAS 2835-06-5, Ampicillin intermediate, Cefalexin intermediate, Pharmaceutical intermediate, Suzhou Health Chemicals Co. Ltd., DL-Phenylglycine manufacturer, DL-Phenylglycine supplier, Beta-lactam antibiotic synthesis, DL-Phenylglycine price, High purity DL-Phenylglycine, Amino acid derivative, Bulk DL-Phenylglycine CAS 2835-06-5

 

DL-alpha-Phenylglycine (CAS 2835-06-5) serves as a vital pharmaceutical intermediate and fine chemical building block, predominantly utilized in the synthesis of broad-spectrum semi-synthetic penicillins (such as Ampicillin) and cephalosporin antibiotics (including Cefalexin, Cefradine, and Cefaclor). Through optical resolution, it acts as the key precursor for D-phenylglycine and L-phenylglycine, which are essential side-chain constructs in chiral drug manufacturing, peptide synthesis, and natural product derivatization. Beyond medicine, it finds key application as a protective group reagent, organic synthesis ligand, and amino acid derivative modifier in biotechnology and advanced chemical research worldwide.