144701-25-7

Basic information

• Product Name: FMOC-D-CHA-OH
• Synonyms: N-ALPHA-FMOC-BETA-CYCLOHEXYL-D-ALANINE;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-HEXAHYDRO-D-PHENYLALANINE;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-CYCLOHEXYLALANINE;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-HEXAHYDROPHENYLALANINE;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-BETA-CYCLOHEXYL-D-ALANINE;RARECHEM EM WB 0095;FMOC-BETA-CYCLOHEXYL-D-ALANINE;FMOC-BETA-CYCLOHEXYL-D-ALA-OH
• CAS NO: 144701-25-7
• Molecular Formula: C₂₄H₂₇NO₄
• Molecular Weight: 393.48
• Product Categories: Amino Acids;Peptide
• Mol File: 144701-25-7.mol

Chemical Properties

• Boiling Point: 610.5 °C at 760 mmHg
• Flash Point: 323 °C
• Appearance: White/Powder
• Density: 1.209 g/cm³
• Vapor Pressure: 9.3E-16mmHg at 25°C
• Refractive Index: 1.589
• Storage Temp.: 2-8°C
• PKA: 3.91±0.10(Predicted)
• CAS DataBase Reference: FMOC-D-CHA-OH(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-D-CHA-OH(144701-25-7)
• EPA Substance Registry System: FMOC-D-CHA-OH(144701-25-7)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• F: 10
• HazardClass: IRRITANT
• Hazardous Substances Data: 144701-25-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
FMOC-D-CHA-OH is used as a fine chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs and medications, contributing to the advancement of medical treatments.
Used in Chemical Research:
In the field of chemical research, FMOC-D-CHA-OH serves as an important compound for studying various chemical reactions and processes. Its white powder form makes it suitable for use in laboratory settings, where it can be manipulated and analyzed to gain insights into its properties and potential applications.
Used in Material Science:
FMOC-D-CHA-OH also finds applications in material science, where it can be used to develop new materials with specific properties. Its unique structure and chemical properties make it a valuable component in the creation of advanced materials for various industries.

InChI:InChI=1/C24H27NO4/c26-23(27)22(14-16-8-2-1-3-9-16)25-24(28)29-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,16,21-22H,1-3,8-9,14-15H2,(H,25,28)(H,26,27)/t22-/m1/s1

Upstream product

• 28920-43-6 (fluorenylmethoxy)carbonyl chloride 
• 4441-50-3 L-2-cyclohexylalanine 

Relevant articles and documents

Site-specific incorporation of non-natural residues into peptides: Effect of residue structure on suppression and translation efficiencies

A systematic survey of the structural requirements for biosynthetic incorporation of non-natural residues into a polypeptide is presented. Relative translation efficiencies for a series of 12 semi-synthetic acylated suppressor tRNAs ranged from 0 to 91% depending on the structure of the residue incorporated.