108811-30-9

Basic information

• Product Name: 6-O-(triphenylmethyl)-β-D-glucopyranosyl-6'-O-(triphenylmethyl)-β-D-glucopyranoside
• Synonyms: 6-O-(triphenylmethyl)-β-D-glucopyranosyl-6'-O-(triphenylmethyl)-β-D-glucopyranoside
• CAS NO: 108811-30-9
• Molecular Weight: 826.94
• Mol File: 108811-30-9.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: 6-O-(triphenylmethyl)-β-D-glucopyranosyl-6'-O-(triphenylmethyl)-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 6-O-(triphenylmethyl)-β-D-glucopyranosyl-6'-O-(triphenylmethyl)-β-D-glucopyranoside(108811-30-9)
• EPA Substance Registry System: 6-O-(triphenylmethyl)-β-D-glucopyranosyl-6'-O-(triphenylmethyl)-β-D-glucopyranoside(108811-30-9)

Safety Data

• Hazardous Substances Data: 108811-30-9(Hazardous Substances Data)

Upstream product

• 499-23-0 β,β-trehalose 
• 76-83-5 trityl chloride 
• 6138-23-4 trehalose dihydrate 
• 99-20-7 TREHALOSE 
• 75869-80-6 2,2',3,3',4,4'-hexa-O-acetyl-6,6'-di-O-trityl-α,α-trehalose 

Downstream Products

• 128188-34-1 2,3,4,2',3',4'-hexa-(benzyloxy)-6,6'-di-(trityloxy)-α,α-trehalose 
• 75869-80-6 2,2',3,3',4,4'-hexa-O-acetyl-6,6'-di-O-trityl-α,α-trehalose 
• 108811-31-0 2,3,4-tri-O-methyl-6-O-(triphenylmethyl) β-D-glucopyranosyl-2'-3'-4'-tri-O-methyl-6'-O-(triphenylmethyl)-β-D-glucopyranoside 
• 108811-28-5 2,3,4-tri-O-methyl-6-O-(triphenylmethyl)-α-D-glucopyranosyl-2',3',4'-tri-O-methyl-6'-O-(triphenylmethyl)-α-D-glucopyranoside 
• 142386-45-6 2,3,4,2',3',4'-hexa-O-benzoyl-6,6'-di-O-triphenylmethyl-α,α-trehalose 
• 128188-34-1 2,3,4,2',3',4'-hexa-O-benzyl-6,6'-di-O-trityl-β,β-trehalose 
• 74501-32-9 2,3,4,2',3',4'-hexa-O-benzyl-6,6'-di-O-trityl-α,α-trehalose 
• 1206468-50-9 C₇₈H₁₃₆N₆O₂₉ 

Relevant articles and documents

Synthesis of macrocycles on the basis of diterpenoid isosteviol and trehalose

Macrocyclic glycoterpenoids containing trehalose and isosteviol fragments have been synthesized. Selective screening has revealed compounds exhibiting antitubercular activity against H37RV, M. Avium and M. Terrae at a level comparable to the known antitub

Dansyl acetyl trehalose: A novel tool to investigate the cellular fate of trehalose

A fluorescent derivative of trehalose with two dansyl groups (DAT) has been synthesized. It is characterised by a large Stokes shift, good permeability in human living cells and a well detectable fluorescent signal within the cells. Notably, in intestinal

An improved synthesis of (2,3,4-tri-O-acetyl-α-D-glucopyranosyl)uronic acid (2,3,4-tri-O-acetyl-α-D-glucopyranosid)uronic acid

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Total Synthesis of an Immunogenic Trehalose Phospholipid from Salmonella Typhi and Elucidation of Its sn-Regiochemistry by Mass Spectrometry

Diphosphatidyltrehalose (diPT) is an immunogenic glycolipid, recently isolated from Salmonella Typhi. Despite rigorous structure elucidation, the sn-position of the acyl chains on the glycerol backbone had not been unequivocally established. A stereoselective synthesis of diPT and its regioisomer is reported herein. Using a hybrid MS3 approach combining collisional dissociation and ultraviolet photodissociation mass spectrometry for analysis of the regioisomers and natural diPT, the regiochemistry of the acyl chains of this abundant immunostimulatory glycolipid was established.