269726-89-8

Basic information

• Product Name: BOC-(R)-3-AMINO-4-(2-THIENYL)-BUTYRIC ACID
• Synonyms: BOC-(R)-3-AMINO-4-(2-THIENYL)BUTANOIC ACID;BOC-(R)-3-AMINO-4-(2-THIENYL)-BUTYRIC ACID;BOC-(2-THIENYL)-D-BETA-HOMOALANINE;BOC-D-BETA-HOALA(2-THIENYL)-OH;BOC-D-ALA(2-THIENYL)-(C*CH2)OH;RARECHEM AK PT B013;N-BETA-T-BUTOXYCARBONYL-D-HOMO(2-THIENYL)ALANINE;N-T-BUTOXYCARBONYL-(R)-3-AMINO-4-(2-THIENYL)BUTANOIC ACID
• CAS NO: 269726-89-8
• Molecular Formula: C13H19NO4S
• Molecular Weight: 285.36
• Product Categories: 3-Amino-4-phenylbutanoic Acid Analogs;B-Amino
• Mol File: 269726-89-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 449.3 °C at 760 mmHg
• Flash Point: 225.6 °C
• Appearance: /
• Density: 1.216
• Vapor Pressure: 7.35E-09mmHg at 25°C
• Refractive Index: 1.538
• Storage Temp.: 2-8°C(protect from light)
• PKA: 4.38±0.10(Predicted)
• CAS DataBase Reference: BOC-(R)-3-AMINO-4-(2-THIENYL)-BUTYRIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-(R)-3-AMINO-4-(2-THIENYL)-BUTYRIC ACID(269726-89-8)
• EPA Substance Registry System: BOC-(R)-3-AMINO-4-(2-THIENYL)-BUTYRIC ACID(269726-89-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 269726-89-8(Hazardous Substances Data)

Usage

General Description

BOC-(R)-3-AMINO-4-(2-THIENYL)-BUTYRIC ACID is a chemical compound that is commonly used in the field of organic chemistry. It is a derivative of amino acid, with a BOC (tert-butyloxycarbonyl) protecting group attached to the amino group. The compound contains a thienyl group, which is a five-membered ring containing four carbon atoms and one sulfur atom. This chemical has potential applications in the synthesis of pharmaceuticals, agrochemicals, and materials. Its structure and properties make it useful for the development of new drugs and biologically active compounds. Additionally, the presence of the BOC protecting group allows for controlled release of the amino group when needed in organic reactions.

InChI:InChI=1/C13H19NO4S/c1-13(2,3)18-12(17)14-9(8-11(15)16)7-10-5-4-6-19-10/h4-6,9H,7-8H2,1-3H3,(H,14,17)(H,15,16)/t9-/m0/s1