Cbz-glycine

CAS: 1138-80-3

Ref. 3D-FC39362

Produktinformation

• Name: Cbz-glycine
• Synonyme: (Carbobenzoxy)glycine, (Carbobenzyloxy)glycine, 2-(Benzyloxycarbonylamino)acetic acid, 2-(Phenylmethoxycarbonylamino)acetic acid, Benzyloxycarbonylglycine, Cbz-Gly-OH, Glycine, N-[(phenylmethoxy)carbonyl]-, Glycine, N-carboxy-, N-benzyl ester, N-(Benzyloxycarbonyl)glycine, N-(Carbobenzoxy)glycine, N-(Carbobenzyloxy)glycine, N-(α-Carbobenzoxy)glycine, N-Benzyloxycarbonylglycin, N-Benzyloxycarbonylglycine, N-CBZ-Glycine N-Carbobenzyloxy-glycine, N-Carboxyglycine N-benzyl ester, N-Cbz-Gly-OH, N-Cbz-glycine, N-[(Phenylmethoxy)carbonyl]glycine, N-[(benzyloxy)carbonyl]glycine{[(benzyloxy)carbonyl]amino}acetate, N-benciloxicarbonilglicina, N-cbz-glycine crystalline, N^α-(Benzyloxycarbonyl)glycine, Nsc 2526, Nα-(Benzyloxycarbonyl)glycine, Z-Gly-OH, Z-glycine, [[(Benzyloxy)carbonyl]amino]acetic acid, z-Gly
• CAS: 1138-80-3

Beschreibung

Cbz-glycine is a hydrogen bond donor that can react with trifluoroacetic acid in a one-step reaction to form an ester hydrochloride. It is used in the synthesis of monoclonal antibodies and has been shown to inhibit the growth of receptor cells. Cbz-glycine reacts with protocatechuic acid, pyrazinoic acid, and ester hydrochloride to form pharmacokinetic properties. It has been shown to have pharmacokinetic properties by inhibiting prostaglandin synthesis.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 209.2 g/mol
• Formel: C₁₀H₁₁NO₄
• Reinheit: Min. 95%
• InChl: InChI=1S/C10H11NO4/c12-9(13)6-11-10(14)15-7-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,11,14)(H,12,13)
• InChI Key: InChIKey=CJUMAFVKTCBCJK-UHFFFAOYSA-N
• SMILES: O=C(O)CNC(=O)OCc1ccccc1