51433-21-7 Usage
Description
Methyl 2-O,3-O-dimethyl-α-D-glucopyranosiduronic acid methyl ester, also known as methyl glucopyranosiduronic acid, is a chemical compound that is an ester derivative of glucopyranosiduronic acid. It is a methyl ester of a sugar acid, and is often used in chemical and pharmaceutical research as a precursor for the synthesis of various carbohydrate derivatives. Methyl 2-O,3-O-dimethyl-α-D-glucopyranosiduronic acid methyl ester is an important intermediate in the production of glycosidic compounds and can be used as a building block for the synthesis of various natural products and pharmaceuticals. Its structure and properties make it a valuable tool in the study of carbohydrate chemistry and drug development.
Uses
Used in Chemical Research:
Methyl 2-O,3-O-dimethyl-α-D-glucopyranosiduronic acid methyl ester is used as a precursor for the synthesis of various carbohydrate derivatives, making it a valuable tool in chemical research.
Used in Pharmaceutical Research:
Methyl 2-O,3-O-dimethyl-α-D-glucopyranosiduronic acid methyl ester is used as an important intermediate in the production of glycosidic compounds, which can be used as building blocks for the synthesis of various natural products and pharmaceuticals.
Used in Carbohydrate Chemistry:
Methyl 2-O,3-O-dimethyl-α-D-glucopyranosiduronic acid methyl ester is used in the study of carbohydrate chemistry due to its unique structure and properties.
Used in Drug Development:
Methyl 2-O,3-O-dimethyl-α-D-glucopyranosiduronic acid methyl ester is used in drug development as a building block for the synthesis of various pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 51433-21-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,3 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51433-21:
(7*5)+(6*1)+(5*4)+(4*3)+(3*3)+(2*2)+(1*1)=87
87 % 10 = 7
So 51433-21-7 is a valid CAS Registry Number.
51433-21-7Relevant articles and documents
Differential reactivity of α- and β-anomers of glycosyl acceptors in glycosylations. A remote consequence of the endo-anomeric effect?
Magaud, Didier,Dolmazon, Rene,Anker, Daniel,Doutheau, Alain,Dory, Yves L.,Deslongchamps, Pierre
, p. 2275 - 2277 (2000)
(equation presented) When phenyl tri-O-benzyl-1-thio-β-D-galactopyranosiduronic acid esters were coupled with a 1/1 mixture of a and β 2,3 di-O-protected D-galactopyranosiduronic acid esters, the β-anomer proved to be more reactive. Data from theoretical
PROCESS OF PREPARATION OF L-IDURONIC ACID AND DERIVATIVES COMPRISING A DECARBOXYLATION/INTRAMOLECULAR CYCLISATION TANDEM REACTION
-
, (2013/04/24)
The present invention relates to a process of preparation of L-iduronic acid and derivatives comprising a decarboxylation/intramolecular cyclisation tandem reaction. The present invention also relates to the intermediates of the process, as well as their use as intermediates in the preparation of Idraparinux.
Synthesis pathway to carbohydrate-derived salicylidene hydrazides as ligands for oxovanadium complexes
Becher,Seidel,Plass,Klemm
, p. 5675 - 5681 (2007/10/03)
Salicylidene hydrazides represent important ligands forming oxovanadium complexes. Carbohydrate-derived chiral salicylidene hydrazides as ligands for metal ion complexation were synthesized for the first time. The pathway of the mild and selective synthesis starts from commercial saccharides like methyl-α-d-glucopyranoside and methyl-α-d-mannopyranoside. All synthesized carbohydrate-derived salicylidene hydrazides are able to form oxovanadium complexes. The mononuclear structure proposed for the complex of 1,2,3,4-tetra-O-methyl-α-d-glucopyranuronic acid salicylidene hydrazide is consistent with the analytical data (NMR, IR and MS).