1246541-59-2

Basic information

• Product Name: bis[4-(docosyloxy)phenyl]methyl alcohol
• Synonyms: bis[4-(docosyloxy)phenyl]methyl alcohol
• CAS NO: 1246541-59-2
• Molecular Weight: 833.419
• Mol File: 1246541-59-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: bis[4-(docosyloxy)phenyl]methyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: bis[4-(docosyloxy)phenyl]methyl alcohol(1246541-59-2)
• EPA Substance Registry System: bis[4-(docosyloxy)phenyl]methyl alcohol(1246541-59-2)

Safety Data

• Hazardous Substances Data: 1246541-59-2(Hazardous Substances Data)

Upstream product

• 1246541-58-1 4,4'-didocosoxybenzophenone 

Downstream Products

• 1394992-05-2 ethyl [bis-(4-docosoxyphenyl)methyl]carbamate 
• 1394991-99-1 Fmoc-Ala-NH-Dpm(C₂₂) 
• 1246541-64-9 Gly-NH-Dpm 
• 1246541-61-6 1,1-di(4-docosyloxyphenyl)methylamine 
• 1246541-62-7 Fmoc-Gly-NH-Dpm(OC₂₂)2 

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.

PRODUCTION METHOD OF OLIGONUCLEOTIDE

The problem of the present invention is provision of a method of producing an n+p-mer oligonucleotide efficiently in a high yield, which includes use of, as a starting material, an n-mer oligonucleotide wherein the 3′-terminal hydroxyl group is protected,