1448242-66-7

Basic information

• Product Name: 3′,4,4′-tri-O-benzyl-2′-O-tert-butyldimethylsilyl-3-O-[(S)-2-methyloctadecanoyl]-2-O-palmitoyl-α,α-D-trehalose
• Synonyms: 3′,4,4′-tri-O-benzyl-2′-O-tert-butyldimethylsilyl-3-O-[(S)-2-methyloctadecanoyl]-2-O-palmitoyl-α,α-D-trehalose
• CAS NO: 1448242-66-7
• Molecular Weight: 1245.84
• Mol File: 1448242-66-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3′,4,4′-tri-O-benzyl-2′-O-tert-butyldimethylsilyl-3-O-[(S)-2-methyloctadecanoyl]-2-O-palmitoyl-α,α-D-trehalose(CAS DataBase Reference)
• NIST Chemistry Reference: 3′,4,4′-tri-O-benzyl-2′-O-tert-butyldimethylsilyl-3-O-[(S)-2-methyloctadecanoyl]-2-O-palmitoyl-α,α-D-trehalose(1448242-66-7)
• EPA Substance Registry System: 3′,4,4′-tri-O-benzyl-2′-O-tert-butyldimethylsilyl-3-O-[(S)-2-methyloctadecanoyl]-2-O-palmitoyl-α,α-D-trehalose(1448242-66-7)

Safety Data

• Hazardous Substances Data: 1448242-66-7(Hazardous Substances Data)

Upstream product

• 1448242-49-6 3,3′-di-O-benzyl-4,6;4′,6′-di-O-benzylidene-2′-O-tert-butyldimethylsilyl-α,α-D-trehalose 
• 127072-92-8 3,3'-di-o-benzyl-4,6,4',6'-di-o-benzylidene-α,α'-D-trehalose 
• 42390-78-3 2,3,4,6,2',3',4',6'-octa-O-trimethylsilyl-α,α-D-trehalose 
• 99-20-7 TREHALOSE 
• 1448242-59-8 (S)-tert-butyl 2-methyloctadecanoate 
• 125440-57-5 Hexadecylmagnesium chloride 
• 100-52-7 benzaldehyde 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 1448242-62-3 3′-O-benzyl-4,6;4′,6′-di-O-benzylidene-2′-O-tert-butyldimethylsilyl-3-O-[(S)-2-methyloctadecanoyl]-2-O-palmitoyl-α,α-D-trehalose 
• 1448242-53-2 3′-O-benzyl-4,6;4′,6′-di-O-benzylidene-2′-O-tert-butyldimethylsilyl-α,α-D-trehalose 

Relevant articles and documents

Synthesis of a mycobacterium tuberculosis tetra-acylated sulfolipid analogue and characterization of the chiral acyl chains using anisotropic NAD 2D-NMR spectroscopy

Tetra-O-acylated sulfolipids are metabolites found in the cell wall of Mycobacterium tuberculosis, the causative agent of tuberculosis. Their role in pathogenesis remains, however, undefined. Here we describe a novel access to model tetra-O-acylated treha