24050-88-2

Basic information

• Product Name: Boc-Pro-Phe-OPic
• CAS NO: 24050-88-2
• Molecular Weight: 453.538
• Mol File: 24050-88-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Boc-Pro-Phe-OPic(CAS DataBase Reference)
• NIST Chemistry Reference: Boc-Pro-Phe-OPic(24050-88-2)
• EPA Substance Registry System: Boc-Pro-Phe-OPic(24050-88-2)

Safety Data

• Hazardous Substances Data: 24050-88-2(Hazardous Substances Data)

Upstream product

• 84891-23-6 L-phenylalanine 4-picolyl ester 
• 15761-39-4 1-(tert-butoxycarbonyl)-L-proline 
• 586-95-8 pyridine-4-methanol 
• 83031-02-1 t-butoxycarbonyl-L-phenylalanine 4-picolyl ester 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 

Downstream Products

• 83031-01-0 Boc-Pro-Pro-Gly-Phe-Ser(Bzl)-Pro-Phe-OPic 
• 83030-90-4 (S)-2-[((S)-1-{(S)-3-Benzyloxy-2-[(S)-3-phenyl-2-(2-{[(S)-1-((S)-pyrrolidine-2-carbonyl)-pyrrolidine-2-carbonyl]-amino}-acetylamino)-propionylamino]-propionyl}-pyrrolidine-2-carbonyl)-amino]-3-phenyl-propionic acid pyridin-4-ylmethyl ester 
• 83031-00-9 Boc-Pro-Gly-Phe-Ser(Bzl)-Pro-Phe-OPic 
• 83030-99-3 Boc-Gly-Phe-Ser(Bzl)-Pro-Phe-OPic 
• 83030-98-2 Boc-Phe-Ser(Bzl)-Pro-Phe-OPic 
• 83030-97-1 Boc-Ser(Bzl)-Pro-Phe-OPic 
• 83030-91-5 N^α-benzyloxycarbonyl-N^ω-nitro-L-arginyl-L-prolyl-L-prolylglycyl-L-phenylalanyl-O-benzyl-L-seryl-L-prolyl-L-phenylalanine 4-picolyl ester 
• 83030-58-4 Boc-Arg(NO₂)-Pro-Pro-Gly-Phe-Ser(Bzl)-Pro-Phe-OPic 
• 83030-59-5 N^α-t-butoxycarbonyl-N^ω-nitro-L-arginyl-L-prolyl-L-prolyl-glycyl-L-phenylalanyl-O-benzyl-L-seryl-L-prolyl-L-phenylalanylhydrazide 
• 83030-92-6 N^α-benzyloxycarbonyl-N^ω-nitro-L-arginyl-L-prolyl-L-prolylglycyl-L-phenylalanyl-O-benzyl-L-seryl-L-prolyl-L-phenylalanine 
• 83030-60-8 N^α-t-butoxycarbonyl-N^ω-nitro-L-arginyl-L-prolyl-L-prolyl-glycyl-L-phenylalanyl-O-benzyl-L-seryl-L-prolyl-L-phenylalanine 
• 47507-91-5 (S)-3-Phenyl-2-[((S)-pyrrolidine-2-carbonyl)-amino]-propionic acid pyridin-4-ylmethyl ester 

Relevant articles and documents

Amino-acids and Peptides. Part 46. Synthesis of Bradykinin Analogues Modified in the Vicinity of the Carboxy-group

In order to investigate further the effect on biological activity of structural changes in the vicinity of the terminal carboxy-group, the following analogues of bradykinin have been synthesised by the picolyl ester method: bradykinyl-L-isoleucine (2), -L