83825-42-7

Basic information

• Product Name: BOC-L-3-THIENYLALANINE DCHA SALT
• Synonyms: T-BUTOXYCARBONYL-BETA-(3-THIENYL)-L-ALANINE DICYCLOHEXYLAMMONIUM SALT;BOC-L-3-THIENYLALANINE-DCHA;BOC-L-3-THIENYLALANINE DCHA SALT;BOC-BETA-(3-THIENYL)-L-ALANINE DICYCLOHEXYLAMMONIUM SALT;BOC-ALA(3-THIENYL)-OH DCHA;BOC-3-ALA(3-THIENYL)-OH DCHA;BOC-3-(3-THIENYL)-L-ALANINE DICYCLOHEXYLAMINE SALT;N-tert-Butoxycarbonyl-3-thienyl-L-alanine
• CAS NO: 83825-42-7
• Molecular Formula: C₁₂H₁₇NO₄S
• Molecular Weight: 271.33
• Product Categories: Amino Acids;Phenylalanine analogs and other aromatic alpha amino acids;a-amino
• Mol File: 83825-42-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 434.7 °C at 760 mmHg
• Flash Point: 216.7 °C
• Appearance: yellow viscous liquid.
• Density: 1.2791 (rough estimate)
• Vapor Pressure: 2.51E-08mmHg at 25°C
• Refractive Index: 1.6280 (estimate)
• Storage Temp.: Store at 0-5°C
• PKA: 3.85±0.10(Predicted)
• CAS DataBase Reference: BOC-L-3-THIENYLALANINE DCHA SALT(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-L-3-THIENYLALANINE DCHA SALT(83825-42-7)
• EPA Substance Registry System: BOC-L-3-THIENYLALANINE DCHA SALT(83825-42-7)

Safety Data

• Hazard Codes: Xi
• WGK Germany: 3
• Hazardous Substances Data: 83825-42-7(Hazardous Substances Data)

Usage

Chemical Properties

off-white powder

InChI:InChI=1/C12H17NO4S/c1-12(2,3)17-11(16)13-9(10(14)15)6-8-4-5-18-7-8/h4-5,7,9H,6H2,1-3H3,(H,13,16)(H,14,15)/t9-/m0/s1

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 3685-51-6 3-(thien-3-yl)-DL-alanine 
• 123-91-1 1,4-dioxane 
• 67206-08-0 2-acetylamino-3-[3]thienyl-propionic acid 

Relevant articles and documents

INHIBITORS OF AKT ACTIVITY

Invented are novel substituted pyridine compounds, the use of such compounds as inhibitors of protein kinase B activity and in the treatment of cancer and arthritis.

Studies on Cyclic Dipeptides, I: Aryl Modifications of cyclo-[Phe-His]

Seven new cyclic dipeptides have been synthesized and tested for their applicability as tools to elucidate the mechanism of formation of mandelonitrile with (SS)-cyclo-[Phe-His] type catalysts. Conformational analyses based on 1H NMR spectra are presented for all prepared cyclic dipeptides.