40163-88-0

Basic information

• Product Name: BOC-MEPHE-OH DCHA
• Synonyms: BOC-MEPHE-OH DCHA;BOC-L-MEPHE-OH DCHA;BOC-N-METHYL-L-PHENYLALANINE DICYCLOHEXYLAMINE SALT;BOC-N-METHYL-L-PHENYLALANINE DICYCLOHEXYLAMMONIUM SALT;BOC-N-ME-PHE DCHA;BOC-N-ME-PHE-OH DCHA;BOC-N-ME-PHE-OH DICYCLOHEXYLAMINE SALT;N-ALPHA-T-BUTOXYCARBONYL-N-ALPHA-METHYL-L-PHENYLALANINE DICYCLOHEXYLAMMONIUM SALT
• CAS NO: 40163-88-0
• Molecular Formula: C27H44N2O4
• Molecular Weight: 460.65
• Product Categories: Amino Acid Derivatives;N-Methyl Amino Acids;Boc-Amino acid series
• Mol File: 40163-88-0.mol
• Article Data: 0

Chemical Properties

• Melting Point: 174-177 °C
• Boiling Point: 587.7 °C at 760 mmHg
• Flash Point: 309.2 °C
• Appearance: /
• Vapor Pressure: 1.17E-14mmHg at 25°C
• Storage Temp.: 2-8°C
• BRN: 6310237
• CAS DataBase Reference: BOC-MEPHE-OH DCHA(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-MEPHE-OH DCHA(40163-88-0)
• EPA Substance Registry System: BOC-MEPHE-OH DCHA(40163-88-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 40163-88-0(Hazardous Substances Data)

Usage

General Description

BOC-MEPHE-OH DCHA is a chemical compound that contains a BOC (tert-butoxycarbonyl) protecting group, MEPHE (N-methyl-N-phenylethyl) amino acid derivative, and a DCHA (dicyclohexylamine) coupling reagent. It is commonly used in organic synthesis and peptide chemistry as a building block for the introduction of MEPHE amino acid into peptide sequences. The BOC protecting group serves to protect the amine functionality of the MEPHE amino acid, while the DCHA coupling reagent facilitates the formation of peptide bonds. Overall, BOC-MEPHE-OH DCHA is an important tool in the synthesis of complex peptides and organic molecules.

InChI:InChI=1/C15H21NO4.C12H23N/c1-15(2,3)20-14(19)16(4)12(13(17)18)10-11-8-6-5-7-9-11;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h5-9,12H,10H2,1-4H3,(H,17,18);11-13H,1-10H2/t12-;/m0./s1