143003-65-0

Basic information

• Product Name: Hexadecanoic acid, 2-hydroxy-3-(phenylmethoxy)propyl ester, (R)-
• CAS NO: 143003-65-0
• Molecular Formula: C26H44O4
• Molecular Weight: 420.633
• Mol File: 143003-65-0.mol

Chemical Properties

• CAS DataBase Reference: Hexadecanoic acid, 2-hydroxy-3-(phenylmethoxy)propyl ester, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Hexadecanoic acid, 2-hydroxy-3-(phenylmethoxy)propyl ester, (R)-(143003-65-0)
• EPA Substance Registry System: Hexadecanoic acid, 2-hydroxy-3-(phenylmethoxy)propyl ester, (R)-(143003-65-0)

Safety Data

• Hazardous Substances Data: 143003-65-0(Hazardous Substances Data)

Upstream product

• 2930-05-4 (S)-benzyl glycidyl ether 
• 57-10-3 1-hexadecylcarboxylic acid 
• 100-39-0 benzyl bromide 
• 693-38-9 vinyl palmitate 
• 17325-85-8 (2S)-3-(benzyloxy)propane-1,2-diol 
• 20196-71-8 (2S)-2,3-bis(benzyloxy)propanol 
• 20196-70-7 (+)-(R)-2,3-bis(benzyloxy)propanal 
• 14347-83-2 (R)-2,2-dimethyl-4-benzoxymethyl-1,3-dioxolane 
• 100-44-7 benzyl chloride 
• 112-67-4 n-hexadecanoyl chloride 
• 29599-41-5 1.2-Dibenzyl-glycerin-3-palmitinsaeureester 

Downstream Products

• 90365-30-3 1-O-benzyl-2,3-di-O-hexadecanoyl-sn-glycerol 
• 6076-30-8 1,2-di-O-palmitoyl-sn-glycerol 
• 1656-83-3 (R)-1-hydroxy-3-(palmitoyloxy)propan-2-yl oleate 
• 51704-36-0 (9Z,12Z)-Octadeca-9,12-dienoic acid (R)-2-hexadecanoyloxy-1-hydroxymethyl-ethyl ester 
• 70094-88-1 1-palmitoyl-2-linoleoyl-3-sn-phosphatidylcholine 
• 907216-71-1 3-hexadecanoyl-1,2-di(cis-hexadec-9-enoyl)-sn-glycerol 
• 65390-75-2 sn-1,2-dioleoyl-3-palmitoylglycerol 
• 19670-51-0 (R)-2,3-dihydroxypropyl n-hexadecanoate 

Relevant articles and documents

Differential interaction of an AmB Analogue and ergosterol in enantiomeric membranes

An amphotericin B derivative exhibits differential interaction with vesicles formed from either natural (R)-or unnatural (S)-POPC and ergosterol. This implicates a close association between the polyene macrolide and the phospholipid bilayer and may account for its increased antifungal activity.

Synthesis of enantiopure structured triacylglycerols

The synthesis of nine enantiopure structured triacylglycerols (TAGs) of the AAB type is described, all possessing the (S)-absolute configuration. Six of them possess one saturated and two identical unsaturated fatty acyl chains, whereas the remaining three possess two identical saturated fatty acids along with one unsaturated fatty acid. The former group was synthesized by a five-step chemoenzymatic route involving a highly regioselective immobilized Candida antarctica lipase, starting from enantiopure (R)-solketal. The second group was prepared by a fully chemical five-step approach based on the same chiral precursor. Such enantiopure TAGs are strongly required as standards for the enantiospecific analysis of intact TAGs in fats and oils.

The efficient synthesis of mixed diacyl phospholipids with polyunsaturated fatty acid in sn-2 position of glycerol

A convenient method for synthesis of the mixed-diacyl phospholipid using boron trichloride as an efficient reagent for the removal of benzyl protecting group from polyunsaturated diacylglycerols without affecting the double bond and acyl migration is desc