1394991-99-1

Basic information

• Product Name: Fmoc-Ala-NH-Dpm(C₂₂)
• Synonyms: Fmoc-Ala-NH-Dpm(C₂₂)
• CAS NO: 1394991-99-1
• Molecular Weight: 1125.76
• Mol File: 1394991-99-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Fmoc-Ala-NH-Dpm(C₂₂)(CAS DataBase Reference)
• NIST Chemistry Reference: Fmoc-Ala-NH-Dpm(C₂₂)(1394991-99-1)
• EPA Substance Registry System: Fmoc-Ala-NH-Dpm(C₂₂)(1394991-99-1)

Safety Data

• Hazardous Substances Data: 1394991-99-1(Hazardous Substances Data)

Upstream product

• 1246541-60-5 ethyl [bis-(4-docosoxyphenyl)methyl]carbamate 
• 1246541-61-6 1,1-di(4-docosyloxyphenyl)methylamine 
• 35661-39-3 N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine 
• 1394992-05-2 ethyl [bis-(4-docosoxyphenyl)methyl]carbamate 
• 1246541-59-2 bis[4-(docosyloxy)phenyl]methyl alcohol 
• 1246541-58-1 4,4'-didocosoxybenzophenone 
• 611-99-4 4,4'-Dihydroxybenzophenone 
• 6938-66-5 1-Bromodocosane 

Relevant articles and documents

Novel diphenylmethyl-derived amide protecting group for efficient liquid-phase peptide synthesis: AJIPHASE

An efficient method for the synthesis of peptides bearing an amide at the C-terminal is described. This method involves the attachment of a C-terminal protecting group bearing long aliphatic chains, followed by the repetition of simple reaction and precipitation steps with the combined advantages of liquid-phase peptide synthesis (LPPS) and solid-phase peptide synthesis (SPPS). Using this method, a hydrophobic peptide was successfully synthesized in good yield and high purity, which cannot be obtained satisfactorily by SPPS.