13035-54-6 Usage
Description
2,3,4,6-tetra-O-acetyl-1-O-(2,4,6-trimethylbenzoyl)hexopyranose is a complex organic compound derived from hexopyranose, a six-carbon sugar. It is acetylated at the 2, 3, 4, and 6 positions and features a benzoyl group attached to the 1 position of the hexopyranose ring. 2,3,4,6-tetra-O-acetyl-1-O-(2,4,6-trimethylbenzoyl)hexopyranose is widely used in carbohydrate chemistry and organic synthesis as a versatile building block for creating more complex molecules, thanks to its acetyl and benzoyl groups.
Uses
Used in Carbohydrate Chemistry:
2,3,4,6-tetra-O-acetyl-1-O-(2,4,6-trimethylbenzoyl)hexopyranose is used as a building block in carbohydrate chemistry for the synthesis of complex carbohydrate structures. Its acetyl and benzoyl groups provide versatility in the formation of various glycosidic linkages and other carbohydrate derivatives.
Used in Organic Synthesis:
In the field of organic synthesis, 2,3,4,6-tetra-O-acetyl-1-O-(2,4,6-trimethylbenzoyl)hexopyranose serves as a starting material for the creation of more intricate organic molecules. Its functional groups allow for a range of chemical reactions, making it suitable for the synthesis of natural products and other bioactive compounds.
Used in Pharmaceutical Industry:
2,3,4,6-tetra-O-acetyl-1-O-(2,4,6-trimethylbenzoyl)hexopyranose is used as a key intermediate in the development of pharmaceutical compounds. Its unique structure and functional groups enable the design and synthesis of novel drug candidates with potential therapeutic applications.
Used in Material Science:
In material science, 2,3,4,6-tetra-O-acetyl-1-O-(2,4,6-trimethylbenzoyl)hexopyranose can be utilized as a component in the synthesis of advanced materials, such as polymers and coatings, that exhibit specific properties due to the presence of the acetyl and benzoyl groups.
Used in Analytical Chemistry:
2,3,4,6-tetra-O-acetyl-1-O-(2,4,6-trimethylbenzoyl)hexopyranose can be employed as a reference compound or a standard in analytical chemistry for the development and validation of methods for the analysis and characterization of complex carbohydrates and related compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 13035-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,3 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13035-54:
(7*1)+(6*3)+(5*0)+(4*3)+(3*5)+(2*5)+(1*4)=66
66 % 10 = 6
So 13035-54-6 is a valid CAS Registry Number.
13035-54-6Relevant articles and documents
Reversing Reactivity: Stereoselective Desulfurative 1,2- trans- O-Glycosylation of Anomeric Thiosugars with Carboxylic Acids under Copper or Cobalt Catalysis
Bennai, Nedjwa,Chabrier, Amélie,Fatthalla, Maha I.,Tran, Christine,Yen-Pon, Expédite,Belkadi, Mohamed,Alami, Mouad,Grimaud, Laurence,Messaoudi, Samir
, p. 8893 - 8909 (2020/08/14)
We have discovered a new mode of reactivity of 1-thiosugars in the presence of Cu(II) or Co(II) for a stereoselective O-glycosylation reaction. The process involves the use of a catalytic amount of Cu(acac)2 or Co(acac)2 and Ag2CO3 as an oxidant in α,α,α-trifluorotoluene. Moreover, this protocol turned out to have a broad scope, allowing the preparation of a wide range of complex substituted O-glycoside esters in good to excellent yields with an exclusive 1,2-trans-selectivity. The late-stage modification of pharmaceuticals by this method was also demonstrated. To obtain a closer insight into the reaction mechanism, cyclic voltammetry was performed.
