68774-48-1

Basic information

• Product Name: 2,5-Anhydro-1-O-triphenylmethyl-D-mannitol
• Synonyms: 2,5-Anhydro-1-O-triphenylmethyl-D-mannitol;2,5-Anhydro-1-O-trityl-D-mannitol min. 98%
• CAS NO: 68774-48-1
• Molecular Formula: C₂₅H₂₆O₅
• Molecular Weight: 406.475
• Product Categories: Sugars
• Mol File: 68774-48-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-Anhydro-1-O-triphenylmethyl-D-mannitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Anhydro-1-O-triphenylmethyl-D-mannitol(68774-48-1)
• EPA Substance Registry System: 2,5-Anhydro-1-O-triphenylmethyl-D-mannitol(68774-48-1)

Safety Data

• Hazardous Substances Data: 68774-48-1(Hazardous Substances Data)

Usage

General Description

2,5-Anhydro-1-O-triphenylmethyl-D-mannitol is a chemical compound with the molecular formula C33H30O5. It is a derivative of D-mannitol, a sugar alcohol commonly found in plants. The compound has a unique structure with a triphenylmethyl group attached to the mannitol molecule. It is commonly used as a protecting group in organic synthesis to block the reactive hydroxyl groups of the mannitol molecule. This allows for selective manipulation of other functional groups without affecting the original hydroxyl groups. 2,5-Anhydro-1-O-triphenylmethyl-D-mannitol is used in the synthesis of various organic compounds and pharmaceuticals, making it an important reagent in chemical research and industry.

Upstream product

• 76-83-5 trityl chloride 
• 41107-82-8 2,5-anhydro-D-mannitol 
• 65758-50-1 2,5-anhydro-1,3-O-isoprpylidene-6-O-triphenylmethyl-D-glucitol 

Downstream Products

• 1146544-48-0 2,5-anhydro-3,4,6-tri-O-benzoyl-D-mannitol 
• 1352744-35-4 (2R,3R,4R,5R)-2-(benzoyloxymethyl)-5-(tosyloxymethyl)tetrahydrofuran-3,4-diyl dibenzoate 
• 1472641-27-2 2,5-anhydro-3,4,6-tri-O-benzoyl-1-fluoro-D-mannitol 
• 1472641-26-1 2,5-anhydro-3,4,6-tri-O-benzoyl-1-O-trityl-D-mannitol 
• 84447-07-4 3,4,6-tri-O-acetyl-2,5-anhydro-1-O-tosyl-D-mannitol 
• 130466-42-1 2,5-anhydro-3,4-di-O-benzyl-1-deoxy-1-diethylphosphono-6-O-diphenylphosphono-D-mannitol 
• 130372-43-9 Acetic acid (2R,3R,4S,5S)-3,4-bis-benzyloxy-5-(diethoxy-phosphorylmethyl)-tetrahydro-furan-2-ylmethyl ester 
• 130465-01-9 ((2S,3S,4R,5R)-3,4-Bis-benzyloxy-5-hydroxymethyl-tetrahydro-furan-2-ylmethyl)-phosphonic acid diethyl ester 
• 102292-67-1 2,5-anhydro-3,4,6-tri-O-benzyl-1-deoxy-1-diethoxyphophinoyl-D-mannitol 
• 109065-80-7 2,5-anhydro-3,4,6-tri-O-benzyl-1-deoxy-1-iodo-D-mannitol 
• 102208-55-9 2,5-anhydro-3,4,6-tri-O-benzyl-D-mannitol 
• 84446-96-8 3,4,6-tri-O-acetyl-2,5-anhydro-1-O-trityl-D-mannitol 

Relevant articles and documents

Synthesis and preliminary evaluation of 1-[18F]Fluoro-1-deoxy-2, 5-anhydro-D-mannitol as a PET radiotracer for breast cancer imaging

1-[18F]Fluoro-1-deoxy-2,5-anhydro-D-mannitol (3, 18F-FDAM) has been synthesized in 6 steps starting from 2,5-anhydro-D-mannitol (2,5-AM) and evaluated as a new radiotracer for PET imaging of MCF-7 breast tumor. The result of PET imag

Analysis of the linkage positions in D-fructofuranosyl residues by the reductive-cleavage method.

The suitability of the reductive-cleavage method for analysis of the linkage positions in D-fructofuranosyl residues of D-fructans was examined by using sucrose, chicory-root inulin, and Aerobacter levanicum levan as models. Permethylation, and reductive