82185-94-2 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 3,6-Di-O-(α-D-Mannopyranosyl)-2-O-(2-propenyl)-α-D-Mannopyranoside Octaacetate is used as an intermediate in the preparation of Methyl 3,6-Di-O-(α-D-mannopyranosyl)-α-D-mannopyranoside (M302500), which is a key compound in the development of pharmaceuticals. Its role in the synthesis process is crucial for creating effective and innovative medications.
Used in Chemical Research:
As a complex organic compound, Methyl 3,6-Di-O-(α-D-Mannopyranosyl)-2-O-(2-propenyl)-α-D-Mannopyranoside Octaacetate is also used in chemical research for studying its properties and potential applications. Researchers can explore its reactivity, stability, and interactions with other compounds, which can lead to the discovery of new uses and advancements in various fields.
Used in Organic Synthesis:
Methyl 3,6-Di-O-(α-D-Mannopyranosyl)-2-O-(2-propenyl)-α-D-Mannopyranoside Octaacetate is utilized in organic synthesis for the creation of various complex molecules and compounds. Its unique structure and properties make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 82185-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,8 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82185-94:
(7*8)+(6*2)+(5*1)+(4*8)+(3*5)+(2*9)+(1*4)=142
142 % 10 = 2
So 82185-94-2 is a valid CAS Registry Number.
82185-94-2Relevant academic research and scientific papers
Syntheses of model oligosaccharides of biological significance. Synthesis of methyl 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-d-mannopyranoside and the corresponding mannobiosides.
Winnik,Brisson,Carver,Krepinsky
, p. 15 - 28 (2007/10/02)
Methyl 2-O-allyl-4,6-O-benzylidene-3-O-(2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranosyl) -alpha-D-mannopyranoside (12) was prepared in 90% yield by Helferich glycosylation of methyl 2-O-allyl-4,6-O-benzylidene-alpha-D-mannopyranoside (9) with tetra-O-acetyl
