18933-87-4

Basic information

• Product Name: 6,6'-diazido-2,2',3,3',4,4'-hexa-O-benzoyl-6,6'-dideoxy-α,α-D-trehalose
• Synonyms: 6,6'-diazido-2,2',3,3',4,4'-hexa-O-benzoyl-6,6'-dideoxy-α,α-D-trehalose
• CAS NO: 18933-87-4
• Molecular Weight: 1016.97
• Mol File: 18933-87-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6,6'-diazido-2,2',3,3',4,4'-hexa-O-benzoyl-6,6'-dideoxy-α,α-D-trehalose(CAS DataBase Reference)
• NIST Chemistry Reference: 6,6'-diazido-2,2',3,3',4,4'-hexa-O-benzoyl-6,6'-dideoxy-α,α-D-trehalose(18933-87-4)
• EPA Substance Registry System: 6,6'-diazido-2,2',3,3',4,4'-hexa-O-benzoyl-6,6'-dideoxy-α,α-D-trehalose(18933-87-4)

Safety Data

• Hazardous Substances Data: 18933-87-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 142386-46-7 2,3,4,2',3',4'-hexakis-O-benzoyl-α,α-D-trehalose 
• 577969-86-9 2,3,2',3'-tetra-O-benzoyl-4,6:4',6'-di-O-benzylidene-α,α-trehalose 
• 18929-82-3 4,6;4',6'-di-O-benzylidene-α,α-D-trehalose 
• 100-52-7 benzaldehyde 
• 99-20-7 TREHALOSE 
• 18933-86-3 6,6'-dibromo-2,3,4,2',3',4'-hexa-O-benzoyl-6,6'-dideoxy-α,α-trehalose 

Downstream Products

• 30923-00-3 6,6'-diamino-6,6'-dideoxy-α,α-D-trehalose 
• 428509-08-4 2,3,4,2',3',4'-hexa-O-benzoyl6,6'-dideoxy-6,6'-bis[(phenylsulfonyl)amino]-α,α-trehalose 
• 428509-05-1 2,3,4,2',3',4'-hexa-O-benzoyl-6,6'-bis[(1-butylsulfonyl)amino]-6,6'-dideoxy-α,α-trehalose 
• 428509-06-2 2,3,4,2',3',4'-hexa-O-benzoyl-6,6'-bis[(1-octylsulfonyl)amino]-6,6'-dideoxy-α,α-trehalose 
• 18933-88-5 6-azido-6-deoxy-α-D-glucopyranosyl-(1→1)-6-azido-6-deoxy-α-D-glucopyranoside 

Relevant articles and documents

Design of Trehalose-Based Amide/Sulfonamide C-type Lectin Receptor Signaling Compounds

Mincle agonists have been shown to induce inflammatory cytokine production, such as tumor necrosis factor-alpha (TNF) and promote the development of a Th1/Th17 immune response that might be crucial to development of effective vaccination against pathogens

Synthesis and biological evaluation of trehalose analogs as potential inhibitors of mycobacterial cell wall biosynthesis

Analogs of trehalose are reported that were designed to interfere with mycolylation pathways in the mycobacterial cell wall. Several derivatives of 6,6′-dideoxytrehalose, including N,N′-dialkylamino and 6,6′-bis(sulfonamido) analogs, were prepared and evaluated for antimycobacterial activity against Mycobacterium tuberculosis H37Ra and a panel of clinical isolates of Mycobacterium avium. 6,6′-Diaminotrehalose and its diazido precursor were both inactive, but significant activity apparently related to aliphatic chain length was found among the sulfonamides, N-alkylamines, and one of the amidines.