136770-76-8

Basic information

• Product Name: 1-O-HEXADECYL-2-DESOXY-2-AMINO-SN-GLYCEROL
• Synonyms: 1-O-HEXADECYL-2-DESOXY-2-AMINO-SN-GLYCEROL
• CAS NO: 136770-76-8
• Molecular Formula: C19H41NO2
• Molecular Weight: 315.53
• Mol File: 136770-76-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: -15°C
• CAS DataBase Reference: 1-O-HEXADECYL-2-DESOXY-2-AMINO-SN-GLYCEROL(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-HEXADECYL-2-DESOXY-2-AMINO-SN-GLYCEROL(136770-76-8)
• EPA Substance Registry System: 1-O-HEXADECYL-2-DESOXY-2-AMINO-SN-GLYCEROL(136770-76-8)

Safety Data

• Hazardous Substances Data: 136770-76-8(Hazardous Substances Data)

Usage

Uses

1-O-Hexadecyl-2-desoxy-2-amino-sn-glycerol is a substrate for human sphingosine kinase.

Upstream product

• 20779-14-0 methanesulfonic acid hexadecyl ester 
• 112-82-3 hexadecanyl bromide 
• 6068-28-6 tosylate de n-hexadecyle 
• 1353577-11-3 (R)-4-(hexadecyloxymethyl)-3-oxazolidin-2-one 
• 1353577-09-9 (4R,αS)-4-(hexadecyloxymethyl)-3-(α-methylbenzyl)oxazolidin-2-one 
• 151312-92-4 4-Hexadecyloxymethyl-2-phenyl-4,5-dihydro-oxazole 

Downstream Products

• 1353577-12-4 (R)-3-hexadecyloxy-(3-(R)-α-methylbenzylureido)prop-2-yl acetate 
• 1353577-15-7 (R)-3-hexadecyloxy-(3-(S)-α-methylbenzylureido)prop-2-yl acetate 
• 136770-77-9 Hexadecanoic acid ((S)-2-hexadecyloxy-1-hydroxymethyl-ethyl)-amide 

Relevant articles and documents

Total synthesis of (R)-(-)-actisonitrile via O-alkylation of optically active 4-hydroxymethyloxazolidin-2-one derivative

The enantioselective synthesis of (R)-(-)-actisonitrile 1 has been achieved via O-alkylation of (4R,αS)-4-hydroxymethyl-3-(α-methylbenzyl) oxazolidin-2-one (αS)-4 with 1-iodohexadecane in the presence of CsOH in DMF. Under these reaction conditions, the O

A convenient synthesis of 1-ether-2-acylamido-2-deoxy-sn- glycerophospholipids

A series of 1-ether-sn-2-acylamidoglycerophospholipids, bearing different polar heads in sn-3-position such as phosphoglycol, -serine, -ethanolamine or -choline, have been prepared. Except for the choline derivative which was synthesized from a β-carbamate alcohol derivative, the remaining compounds were obtained from β-amidoalcohols.