627466-98-2 Usage
Description
2,3,4,6-Tetra-O-benzoyl-D-mannopyranose, with the CAS number 627466-98-2, is a white solid compound that is primarily utilized in the field of organic synthesis. It is a derivative of D-mannopyranose, a monosaccharide, where four of its hydroxyl groups are esterified with benzoyl groups. This modification provides the compound with unique chemical properties that make it valuable for various applications in organic chemistry.
Uses
Used in Organic Synthesis:
2,3,4,6-Tetra-O-benzoyl-D-mannopyranose is used as an intermediate in organic synthesis for the production of various complex organic molecules. Its unique structure and reactivity make it a versatile building block for the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3,4,6-Tetra-O-benzoyl-D-mannopyranose is used as a key component in the synthesis of glycoconjugates, which are molecules that consist of a carbohydrate moiety covalently attached to a non-carbohydrate moiety, such as a protein or lipid. These glycoconjugates play crucial roles in various biological processes, including cell adhesion, immune response, and protein folding. The synthesis of these molecules using 2,3,4,6-Tetra-O-benzoyl-D-mannopyranose can lead to the development of novel therapeutic agents with improved efficacy and selectivity.
Used in Material Science:
2,3,4,6-Tetra-O-benzoyl-D-mannopyranose can also be used in the development of advanced materials, such as polymers and coatings, due to its unique chemical properties. The incorporation of this compound into the structure of these materials can result in improved properties, such as enhanced stability, increased resistance to degradation, and improved biocompatibility.
Used in Analytical Chemistry:
As a reference compound, 2,3,4,6-Tetra-O-benzoyl-D-mannopyranose can be employed in analytical chemistry for the calibration of instruments and the development of new analytical methods. Its unique chemical properties and well-defined structure make it an ideal candidate for these applications, allowing for accurate and reliable measurements in various analytical techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 627466-98-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,7,4,6 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 627466-98:
(8*6)+(7*2)+(6*7)+(5*4)+(4*6)+(3*6)+(2*9)+(1*8)=192
192 % 10 = 2
So 627466-98-2 is a valid CAS Registry Number.
InChI:InChI=1/C34H28O10/c35-30(22-13-5-1-6-14-22)40-21-26-27(42-31(36)23-15-7-2-8-16-23)28(43-32(37)24-17-9-3-10-18-24)29(34(39)41-26)44-33(38)25-19-11-4-12-20-25/h1-20,26-29,34,39H,21H2/t26-,27-,28+,29+,34?/m1/s1
627466-98-2Relevant articles and documents
Synthesis of a Glycosylphosphatidylinositol (GPI) Fragment as a Potential Substrate for Mannoprotein Transglycosidases
Belz, Tyson F.,Williams, Spencer J.
, p. 2053 - 2058 (2021/08/31)
A glycophosphatidylinositol tetrasaccharide fragment was synthesized to mimic the core features of primary model, that of Saccharomyces cerevisiae. The salient feature of this approach is centered on the quick access to various α-1,2- and α-1,6-mannosyl a
3 - monosaccharide acid oxygen glucoside oleanolic alkane type and wusu alkane triterpene saponin derivative and its preparation method and application
-
Paragraph 0035; 0038; 0113, (2017/08/25)
The invention discloses a 3-monouronic acid o-glycoside oleanane type and ursane type triterpenoid saponin derivative. The derivative has a structural formula as shown in the specification, wherein R4 is one of H atom, alkyl containing 1-10 carbons, alkyl
Unexpected stereocontrolled access to 1α,1′β-disaccharides from methyl 1,2-ortho esters
Uriel, Clara,Ventura, Juan,Gomez, Ana M.,Lopez, J. Cristobal,Fraser-Reid, Bert
experimental part, p. 795 - 800 (2012/03/22)
Mannopyranose-derived methyl 1,2-orthoacetates (R = Me) and 1,2-orthobenzoates (R = Ph) undergo stereoselective formation of 1α,1′β-disaccharides, upon treatment with BF 3?Et2O in CH2Cl2, rather than the expected acid-catalyzed reaction leading to methyl glycosides by way of a rearrangement-glycosylation process of the liberated methanol.
