20590-53-8

Basic information

• Product Name: 1,2-O-ISOPROPYLIDENE-5-O-TRIPHENYLMETHYL-ALPHA-D-XYLOFURANOSIDE
• Synonyms: 1,2-O-ISOPROPYLIDENE-5-O-TRIPHENYLMETHYL-ALPHA-D-XYLOFURANOSIDE;1,2-O-(1-Methylethylidene)-5-O-(triphenylMethyl)-alpha-D-xylofuranose;(3aR,5R,6S,6aR)-2,2-dimethyl-5-((trityloxy)methyl)tetrahydrofuro[2,3-d][1,3]dioxol-6-ol(WX191813)
• CAS NO: 20590-53-8
• Molecular Formula: C₂₇H₂₈O₅
• Molecular Weight: 432.50822
• Mol File: 20590-53-8.mol
• Article Data: 23

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-O-ISOPROPYLIDENE-5-O-TRIPHENYLMETHYL-ALPHA-D-XYLOFURANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-O-ISOPROPYLIDENE-5-O-TRIPHENYLMETHYL-ALPHA-D-XYLOFURANOSIDE(20590-53-8)
• EPA Substance Registry System: 1,2-O-ISOPROPYLIDENE-5-O-TRIPHENYLMETHYL-ALPHA-D-XYLOFURANOSIDE(20590-53-8)

Safety Data

• Hazardous Substances Data: 20590-53-8(Hazardous Substances Data)

Usage

General Description

1,2-O-ISOPROPYLIDENE-5-O-TRIPHENYLMETHYL-ALPHA-D-XYLOFURANOSIDE is a complex chemical compound with a complicated name. It is an isopropylidene derivative of alpha-D-xylofuranose, a type of sugar molecule. The presence of triphenylmethyl group in the compound makes it relatively stable and inert, and it is commonly used as a protecting group for the hydroxyl group in organic synthesis. 1,2-O-ISOPROPYLIDENE-5-O-TRIPHENYLMETHYL-ALPHA-D-XYLOFURANOSIDE has potential applications in pharmaceuticals and biotechnology as a building block for more complex molecules due to its unique structure and reactivity. Additionally, it could also find use as a chiral building block in the synthesis of various stereochemically pure compounds.

Upstream product

• 532-20-7 α-D-xylofuranose 
• 532-20-7 D-xylofuranose 
• 87-72-9 D-Xylose 
• 1352550-60-7 3-O-chloroacetyl-1,2-O-isopropylidene-5-O-trityl-α-D-xylofuranose 
• 76-83-5 trityl chloride 
• 20881-04-3 1,2:3,5-di-O-isopropylidene-D-xylofuranose 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 141561-63-9 (((3-methylbut-2-en-1-yl)oxy)methanetrityl)tribenzene 
• 312493-51-9 (((4-methoxybenzyl)oxy)methanetriyl)tribenzene 

Downstream Products

• 67850-91-3 O¹,O²-isopropylidene-O³-methyl-O⁵-trityl-α-D-xylofuranose 
• 226256-01-5 3-S-(benzothiazol-2-yl)-1,2-O-isopropylidene-3-thio-5-O-trityl-α-D-ribofuranose 
• 114861-25-5 (3R,5S)-5-(benzyloxymethyl)tetrahydrofuran-2,3-diol 
• 132454-68-3 (3R,5S)-5-(benzyloxymethyl)-3-hydroxy-dihydrofuran-2(3H)-one 
• 116306-89-9 (3αR,5S,6αR)-5-(benzyloxymethyl)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole 
• 92757-18-1 (4R,6S)-6-(benzyloxy)methyl-4-hydroxy-tetrahydro-2-pyrone 
• 133765-69-2 (3R,5S)-5-Benzyloxymethyl-3-(tert-butyl-dimethyl-silanyloxy)-dihydro-furan-2-one 
• 133765-68-1 (4R,6S)-6-benzyloxymethyl-4-t-butyldimethylsilyloxytetrahydro-2-pyrone 
• 892499-34-2 5-O-trityl-3-O-butyl-1,2-isopropylidene-α-D-xylopyranoside 
• 1094541-32-8 5-O-trityl-3-O-ethyl-1,2-isopropylidene-α-D-xylopyranoside 
• 1094541-33-9 5-O-trityl-3-O-propyl-1,2-isopropylidene-α-D-xylopyranoside 
• 952057-96-4 (Z)-3-deoxy-3-C-[(ethoxycarbonyl)methylene]-1,2-O-isopropylidene-5-O-triphenylmethyl-α-D-erythro-pentose 
• 1030604-48-8 3-phenyl-2H-furo[2,3-c]pyran-2-one 

Relevant articles and documents

Karrikins from plant smoke modulate bacterial quorum sensing

The discovery that plant smoke contains germination stimuli has led to the identification of a new class of signaling molecules named karrikins. Here we report a potential second role for these molecules: in various bacterial species-A. tumefaciens, P. aeruginosa and V. harveyi-they modulate bacterial quorum-sensing (QS), with very different outcomes. the Partner Organisations 2014.

Visible-Light-Mediated, Chemo- and Stereoselective Radical Process for the Synthesis of C-Glycoamino Acids

An approach for efficient synthesis of C-glycosyl amino acids is described. Different from typical photoredox-catalyzed reactions of imines, the new process follows a pathway in which α-imino esters serve as electrophiles in chemoselective addition reactions with nucleophilic glycosyl radicals. The process is highlighted by the mild nature of the reaction conditions, the highly stereoselectivity attending C-C bond formation, and its applicability to C-glycosylations using both armed and disarmed pentose and hexose derivatives.

CYCLIC DI-NUCLEOTIDE COMPOUNDS AND METHODS OF USE

Disclosed are cyclic-di-nucleotide cGAMP analogs, methods of synthesizing the compounds, pharmaceutical compositions comprising the compounds thereof, and use of compounds and compositions in medical therapy.