100167-06-4

Basic information

• Product Name: TCBOC-Phe-OH
• Synonyms: TCBOC-Phe-OH
• CAS NO: 100167-06-4
• Molecular Weight: 368.644
• Mol File: 100167-06-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 481.6±45.0 °C(Predicted)
• Density: 1.402±0.06 g/cm3(Predicted)
• CAS DataBase Reference: TCBOC-Phe-OH(CAS DataBase Reference)
• NIST Chemistry Reference: TCBOC-Phe-OH(100167-06-4)
• EPA Substance Registry System: TCBOC-Phe-OH(100167-06-4)

Safety Data

• Hazardous Substances Data: 100167-06-4(Hazardous Substances Data)

Upstream product

• 63-91-2 L-phenylalanine 
• 66270-36-8 2,2,2-trichloro-1,1-dimethylethoxychloroformate 

Downstream Products

• 134982-29-9 TCBOC-Phe-Leu-OtBu 
• 28635-78-1 L-phenylalanyl-L-leucine tert-butyl ester 

Relevant articles and documents

Total Masking -Gly Bonds by Highly Lipophilic and Chromophoric Ferrocenylmethyl Residue in Peptide Syntheses of Hexaglycine and Leu-Enkephalin

Highly lipophilic and chromophoric ferrocenylmethyl residue is applied to syntheses of peptides hexaglycine and Leu-enkephalin, masking therein all -Gly bonds.Thereby Fem groups influence properties of Fem-peptide derivatives advantageously both in chemosyntheses and cleaning operations, leading to constantly high yields et each step.Despite of its volumous dimension the Fem residue can be introduced into each peptide bond of oligoglycine by succeeding one another of building blocks of H-Fem-Gly-OMe.Strong alkaline conditions during the hydrolyses of methyl esters occurring several times in peptide derivatives do not influence the Gly-Gly-bond at all.Total protected derivatives BOC-(Fem-Gly-)6-OMe and BOC-Tyr(t-Bu)-(Fem-Gly-)2Phe-Leu-OtBu even are soluble in hexane/ethylacetate (1:1).