73994-89-5

Basic information

• Product Name: L-Leucine, N-(N-glycyl-L-phenylalanyl)-, phenylmethyl ester
• CAS NO: 73994-89-5
• Molecular Formula: C24H31N3O4
• Molecular Weight: 425.528
• Mol File: 73994-89-5.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: L-Leucine, N-(N-glycyl-L-phenylalanyl)-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Leucine, N-(N-glycyl-L-phenylalanyl)-, phenylmethyl ester(73994-89-5)
• EPA Substance Registry System: L-Leucine, N-(N-glycyl-L-phenylalanyl)-, phenylmethyl ester(73994-89-5)

Safety Data

• Hazardous Substances Data: 73994-89-5(Hazardous Substances Data)

Upstream product

• 88099-26-7 2-{2-[2-(2-Chloro-3H-inden-1-ylmethoxycarbonylamino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid benzyl ester 
• 1738-77-8 (S)-benzyl 4-methyl-2-(4-methylphenylsulfonamido)pentanoate 
• 88099-25-6 2-[2-(2-Chloro-3H-inden-1-ylmethoxycarbonylamino)-3-phenyl-propionylamino]-4-methyl-pentanoic acid benzyl ester 
• 123150-56-1 2-[2-(3H-Cyclopenta[b]naphthalen-1-ylmethoxycarbonylamino)-3-phenyl-propionylamino]-4-methyl-pentanoic acid benzyl ester 
• 63649-15-0 2-(2-Amino-3-phenyl-propionylamino)-4-methyl-pentanoic acid benzyl ester 
• 80089-22-1 L-leucine (phenylmethyl)ester 
• 63649-15-0 L-phenylalanyl-L-leucine benzyl ester 
• 103321-49-9 9H-fluoren-9-ylmethyl (2-chloro-2-oxoethyl)carbamate 
• 132090-35-8 Boc₂-Gly-Phe-Leu-OBzl 
• 73994-88-4 Boc-Gly-Phe-Leu-OBzl 
• 81184-10-3 HCl*H-Gly-Phe-Leu-OBzl 
• 160617-39-0 Fmoc-Gly-Phe-Leu-OBzl 
• 98908-57-7 Z(OMe)-Gly-Phe-Leu-OBzl 
• 103321-57-9 2S-flouren-9-ylmethoxycarbonylamino-3-phenylpropionyl chloride 

Downstream Products

• 88099-27-8 2-(2-{2-[2-(2-Chloro-3H-inden-1-ylmethoxycarbonylamino)-acetylamino]-acetylamino}-3-phenyl-propionylamino)-4-methyl-pentanoic acid benzyl ester 
• 73994-90-8 glycyl-L-phenylalanyl-L-leucine benzyl ester p-toluenesulfonate 
• 69729-14-2 benzyl ester of N-tert-butoxycarbonylglycylglycylphenylalanylleucine 
• 69729-07-3 H-Gly-Gly-Phe-Leu-OBzl 
• 88099-29-0 Fmoc-Tyr(Bzl)-Gly-Gly-Phe-Leu-OBzl 
• 100930-01-6 Tyr-Gly-Gly-Phe-Leu formate 
• 58822-25-6 Leu-enkephalin 
• 103607-09-6 Z(OMe)-Tyr-D-Pro-Gly-Phe-Leu-OBzl 
• 103607-09-6 Z(OMe)-Tyr-Pro-Gly-Phe-Leu-OBzl 
• 103607-18-7 H-Tyr-D-Pro-Gly-Phe-Leu-OBzl acetate 
• 103607-18-7 H-Tyr-Pro-Gly-Phe-Leu-OBzl acetate 
• 103607-08-5 H-D-Pro-Gly-Phe-Leu-OBzl 
• 103607-08-5 H-Pro-Gly-Phe-Leu-OBzl 
• 77511-32-1 5>-enkephalin 

Relevant articles and documents

Method of producing peptide

The present invention is related to a method of producing a peptide, characterized in contacting a reaction mixture with a base after a condensation reaction to hydrolyze while a basic condition is maintained until a ratio of a remaining unreacted active

Synthesis of [Leu5]enkephalin using Fmoc-Amino Acid Chlorides/KOAt

The coupling of Fmoc-amino acid chlorides can be mediated by the potassium salt of 1-hydroxy-7-azabenzotriazole. Thus the synthesis of [Leu5]enkephalin has been accomplished in good yield and purity.

Bis(BOC) Amino Acid Fluorides as Reactive Peptide Coupling Reagents

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