201421-14-9

Basic information

• Product Name: BOC-D-PEN(ACM)-OH
• Synonyms: N-ALPHA-T-BUTOXYCARBONYL-S-ACETAMIDOMETHYL-D-PENICILLAMINE;N-ALPHA-T-BOC-S-ACETAMIDOMETHYL-D-PENICILLAMINE;N-ALPHA-T-BUTOXYCARBONYL-BETA,BETA-DIMETHYL-S-ACETAMIDOMETHYL-D-CYSTEINE;BOC-D-PEN(ACM)-OH;BOC-D-PENICILLAMINE(ACM)-OH;BOC-D-CYS(ME 2)(ACM)-OH;BOC-BETA,BETA-DIMETHYL-D-CYS(ACM)-OH;BOC-S-ACETAMIDOMETHYL-D-PENICILLAMINE
• CAS NO: 201421-14-9
• Molecular Formula: C13H24N2O5S
• Molecular Weight: 320.41
• Mol File: 201421-14-9.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 532.3±50.0 °C(Predicted)
• Appearance: /
• Density: 1.184±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.54±0.10(Predicted)
• CAS DataBase Reference: BOC-D-PEN(ACM)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-D-PEN(ACM)-OH(201421-14-9)
• EPA Substance Registry System: BOC-D-PEN(ACM)-OH(201421-14-9)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 201421-14-9(Hazardous Substances Data)

Usage

General Description

BOC-D-PEN(ACM)-OH is a chemical compound mainly used as a protective group for amino acids. It consists of a BOC (tert-butyloxycarbonyl) protecting group attached to the amino group of an amino acid, specifically the penicillamine amino acid. BOC-D-PEN(ACM)-OH is often used in peptide synthesis to protect the amino group of penicillamine during the coupling reactions, allowing for selective deprotection and further manipulation. BOC-D-PEN(ACM)-OH is commonly utilized in the production of pharmaceuticals and other bioactive molecules, where the protection of specific functional groups is necessary for the controlled synthesis of the desired compounds.