53685-07-7

Usage

Uses

Used in Organic Synthesis:
Methyl 3,4-O-Isopropylidene-6-O-trityl-α-D-galactopyranoside is used as a key intermediate in organic synthesis for the development of various complex organic molecules. Its unique structure allows it to participate in a wide range of chemical reactions, making it a versatile building block for creating novel compounds with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methyl 3,4-O-Isopropylidene-6-O-trityl-α-D-galactopyranoside is used as a starting material for the synthesis of various pharmaceutical compounds. Its unique chemical properties enable the development of new drugs with improved efficacy and reduced side effects, contributing to the advancement of medical treatments.
Used in Chemical Research:
Methyl 3,4-O-Isopropylidene-6-O-trityl-α-D-galactopyranoside is also utilized in chemical research as a model compound for studying the properties and reactivity of complex organic molecules. Its unique structure provides valuable insights into the behavior of similar compounds, aiding in the development of new synthetic strategies and methodologies.
Used in Material Science:
In the field of material science, Methyl 3,4-O-Isopropylidene-6-O-trityl-α-D-galactopyranoside is used as a component in the development of novel materials with specific properties. Its unique chemical structure can be exploited to create materials with enhanced performance characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.

InChI:InChI=1/C29H32O6/c1-28(2)34-25-23(33-27(31-3)24(30)26(25)35-28)19-32-29(20-13-7-4-8-14-20,21-15-9-5-10-16-21)22-17-11-6-12-18-22/h4-18,23-27,30H,19H2,1-3H3/t23?,24?,25-,26?,27-/m0/s1

Upstream product

• 3396-99-4 methyl α-D-galactopyranoside 
• 76-83-5 trityl chloride 
• 40269-01-0 methyl 3,4-O-isopropylidene-α-D-galactopyranoside 

Downstream Products

• 100221-37-2 methyl 2-O-acetyl-3,4-O-isopropylidene-6-O-trityl-α-D-galactopyranoside 
• 53685-08-8 methyl 2-O-benzyl-3,4-O-isopropylidene-6-O-trityl-α-D-galactopyranoside 
• 100221-38-3 Benzoic acid (3aS,4R,6S,7R,7aS)-6-methoxy-2,2-dimethyl-4-trityloxymethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl ester 
• 3971-45-7 methyl 2-deoxy-α-D-galactopyranoside 
• 128554-61-0 Methyl 4-O-acetyl-2-O-benzyl-3,6-di-O-p-tolylsulfonyl-α-D-galactopyranoside 
• 128554-60-9 C₂₂H₂₄O₉S 
• 128536-92-5 Methyl 4-azido-3,6-di-O-benzoyl-2,4-dideoxy-α-D-arabino-hexopyranoside 
• 128536-91-4 Methyl 3,6-di-O-benzoyl-2-deoxy-α-D-lyxo-hexopyranoside 
• 88087-56-3 methyl 2-O-benzoyl-α-D-galactopyranoside 
• 81348-16-5 methyl 2-O-benzyl-α-D-galactopyranoside 
• 18311-26-7 methyl 6-O-triphenylmethyl-α-D-galactopyranoside 
• 69182-49-6 methyl 3,4-O-isopropylidene-2-O-methyl-6-O-trityl-α-D-galactopyranoside 
• 118314-54-8 methyl 3,4-O-isopropylidene-6-O-trityl-α-D-galactopyranoside 2-(barium sulphate) 
• 130163-34-7 methyl 3,4-O-isopropylidene-6-O-trityl-α-D-galactopyranoside 2-(potassium sulphate) 

Relevant academic research and scientific papers

Novel synthesis of monosulphated methyl α-D-galactopyranosides

The syntheses of the methyl α-D-galactopyranoside 2-,3-,4-, and 6-sulphates (11, 12, 16, and 21 respectively) have been achieved using trimethylamine - sulphur trioxide as a sulphating agent.The procedure used is high yielding and requires shorter reactio

Synthesis and biological activities of methyl oligobiosaminide and some deoxy isomers thereof.

Methyl oligobiosaminide (1) the core structure of oligostatin C, and five analogues, the 6-hydroxy-(2), 2-deoxy- (3), 2-deoxy-6-hydroxy- (4), 3-deoxy- (5), and 3-deoxy-6-hydroxy derivatives (6), were synthesized by coupling the protected pseudo-sugar epoxide 46 with suitable methyl 4-amino-4-deoxy-alpha-D-hexopyranoside derivatives. Compounds 3 and 6 showed notable inhibitory activity against alpha-D-glucosidase and alpha-D-mannosidase, respectively, whereas compound 1 had almost no activity.

2-Substituted methyl alpha-D-galactopyranosides: synthesis and binding affinity for the A and B subunits of the Griffonia simplicifolia I isolectins.

The binding affinities of the N-acetyl, N-trifluoroacetyl, N-propionyl, N-formyl, N-benzoyl, N-p-nitrobenzoyl, N-p-aminobenzoyl, and N-methyl derivatives of methyl 2-amino-2-deoxy-alpha-D-galactopyranoside and the 2-O-acetyl, -benzoyl, -benzyl, and -methyl derivatives of methyl alpha-D-galactopyranoside for the A and B subunits of the Griffonia simplicifolia I isolectins have been determined by hapten inhibition analysis of a galactomannan-isolectin precipitation system. Models for these carbohydrate-protein interactions are presented together with an interpretation of the results on the basis of electronic and steric effects.