69182-49-6 Usage
Uses
Used in Organic Synthesis:
Methyl 3,4-O-Isopropylidene-2-O-methyl-6-O-trityl-α-D-galactopyranoside is used as a synthetic intermediate for the preparation of various complex organic molecules. Its unique structural features, such as the isopropylidine and methyl protecting groups, make it a versatile building block in the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Carbohydrate Chemistry:
In the field of carbohydrate chemistry, Methyl 3,4-O-Isopropylidene-2-O-methyl-6-O-trityl-α-D-galactopyranoside serves as a key intermediate for the synthesis of various carbohydrate derivatives. Its trityl group provides a convenient handle for further functionalization and modification, enabling the development of novel carbohydrate-based compounds with potential applications in drug discovery, diagnostics, and materials science.
Used in Medicinal Chemistry:
Methyl 3,4-O-Isopropylidene-2-O-methyl-6-O-trityl-α-D-galactopyranoside is also utilized in medicinal chemistry as a precursor for the synthesis of bioactive compounds. Its unique structural features can be exploited to design and develop new pharmaceutical agents with improved potency, selectivity, and pharmacokinetic properties.
Used in Chemical Research:
In addition to its practical applications, Methyl 3,4-O-Isopropylidene-2-O-methyl-6-O-trityl-α-D-galactopyranoside is also employed as a research tool in various chemical studies. Its reactivity and structural features make it an attractive candidate for investigating new reaction mechanisms, exploring novel synthetic methodologies, and understanding the fundamental principles of organic chemistry.
Overall, Methyl 3,4-O-Isopropylidene-2-O-methyl-6-O-trityl-α-D-galactopyranoside is a versatile and valuable compound in the realm of organic synthesis, with a wide range of applications across various industries and research fields. Its unique structural features and reactivity make it an essential component in the development of new chemical entities and the advancement of chemical science.
Check Digit Verification of cas no
The CAS Registry Mumber 69182-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,8 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69182-49:
(7*6)+(6*9)+(5*1)+(4*8)+(3*2)+(2*4)+(1*9)=156
156 % 10 = 6
So 69182-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C30H34O6/c1-29(2)35-25-24(34-28(32-4)27(31-3)26(25)36-29)20-33-30(21-14-8-5-9-15-21,22-16-10-6-11-17-22)23-18-12-7-13-19-23/h5-19,24-28H,20H2,1-4H3/t24?,25-,26?,27?,28-/m0/s1
69182-49-6Relevant academic research and scientific papers
2-Substituted methyl alpha-D-galactopyranosides: synthesis and binding affinity for the A and B subunits of the Griffonia simplicifolia I isolectins.
Kaifu,Plantefaber,Goldstein
, p. 37 - 49 (2007/10/02)
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.
