448959-69-1

Basic information

• Product Name: Carbamic acid, [(1R)-2-[(4-decylphenyl)amino]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester
• CAS NO: 448959-69-1
• Molecular Formula: C31H46N2O4
• Molecular Weight: 510.717
• Mol File: 448959-69-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [(1R)-2-[(4-decylphenyl)amino]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [(1R)-2-[(4-decylphenyl)amino]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester(448959-69-1)
• EPA Substance Registry System: Carbamic acid, [(1R)-2-[(4-decylphenyl)amino]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester(448959-69-1)

Safety Data

• Hazardous Substances Data: 448959-69-1(Hazardous Substances Data)

Upstream product

• 104-42-7 4-dodecylaniline 
• 47173-80-8 N-Boc-D-serine(Bzl)-OH 
• 37529-30-9 4-n-decylaniline 

Downstream Products

• 448959-77-1 [1-(4-decyl-phenylcarbamoyl)-2-(di-tert-butoxy-phosphoryloxy)-ethyl]-carbamic acid tert-butyl ester 
• 448959-73-7 [1-(4-decyl-phenylcarbamoyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester 

Relevant articles and documents

NOVEL LYSOPHOSPHATIDIC ACID RECEPTOR SELECTIVE ANTAGONISTS

The present invention is directed to compositions comprising lysophosphatidic acid analogs and methods of using such analogs as agonist or antagonists of LPA receptor activity. In addition the invention is directed to LPA receptor agonists that vary in the degree of selectivity at individual LPA receptors (i.e. LPA1, LPA2 and LPA3). More particularly the present invention is directed to LPA analogs wherein the glycerol is replaced with ethanolamine and a variety of substitutions have been linked at the second carbon atom.

Synthesis of Para-alkyl aryl amide analogues of sphingosine-1-phosphate: Discovery of potent S1P receptor agonists

Sphingosine-1-phosphate (S1P) is a biologically active lysophospholipid with the capacity to induce a broad range of cellular responses via its interaction with the S1P family of G-protein coupled receptors. This report describes the synthesis of several