59571-75-4 Usage
Description
ALPHA-D-MAN-[1->2]-ALPHA-D-MAN-1->OME, also known as methyl 2-O-(alpha-D-mannopyranosyl)-alpha-D-mannopyranoside, is a white amorphous solid with unique chemical properties. It is a compound that plays a significant role in organic synthesis and serves as a substrate for specific enzymes.
Uses
1. Enzyme Substrate:
ALPHA-D-MAN-[1->2]-ALPHA-D-MAN-1->OME is used as a substrate for the linkage-specific 1,2-α-mannosidase from Aspergillus niger. This application is crucial for studying the enzyme's activity and its role in various biological processes.
2. Organic Synthesis:
In the field of organic synthesis, ALPHA-D-MAN-[1->2]-ALPHA-D-MAN-1->OME is used as a compound that contributes to the development of new chemical entities. Its unique structure allows for the creation of various complex molecules with potential applications in different industries.
3. Pharmaceutical Industry:
Used in the Pharmaceutical Industry, ALPHA-D-MAN-[1->2]-ALPHA-D-MAN-1->OME serves as a key intermediate in the synthesis of various pharmaceutical compounds. Its role in this industry is vital for the development of new drugs and therapies.
4. Research and Development:
ALPHA-D-MAN-[1->2]-ALPHA-D-MAN-1->OME is also used in research and development for its potential applications in understanding the structure and function of complex carbohydrates and their interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 59571-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,7 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59571-75:
(7*5)+(6*9)+(5*5)+(4*7)+(3*1)+(2*7)+(1*5)=164
164 % 10 = 4
So 59571-75-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O11/c1-21-13-11(9(19)7(17)5(3-15)23-13)24-12-10(20)8(18)6(16)4(2-14)22-12/h4-20H,2-3H2,1H3/t4-,5-,6-,7-,8+,9+,10+,11+,12-,13+/m1/s1
59571-75-4Relevant articles and documents
Chemoenzymatic synthesis of GDP-azidodeoxymannoses: Non-radioactive probes for mannosyltransferase activity
Marchesan, Silvia,Macmillan, Derek
supporting information; experimental part, p. 4321 - 4323 (2009/03/12)
GDP-2-, 3-, 4- or 6-azidomannoses can be successfully prepared from the corresponding azidomannose-1-phosphates and GTP using the enzyme GDP-Mannosepyrophosphorylase (GDP-ManPP) from Salmonella enterica and may serve as useful probes for mannosyltransferase activity. The Royal Society of Chemistry.
A SIMPLE STRATEGY FOR CHANGING THE REGIOSELECTIVITY OF GLYCOSIDASE-CATALYSED FORMATION OF DISACCHARIDES
Nilsson, Kurt G. I.
, p. 95 - 104 (2007/10/02)
The regioselectivity of glycosidase-catalysed formation of disaccharides can be changed by using α- or β-glycosyl acceptors with various aglycons.The preponderant formation of other than (1->6) linkages can be effected with glycosidases which normally give (1->6) linkages.Thus, an α-D-galactosidase can be induced to catalyse the formation mainly of α-(1->2)-, α-(1->3)-, or α-(1->6)-linked digalctosides.Both the structure of the aglycon and the configuration of the glycosidic linkage can have a pronounced influence on the regioselectivity of disaccharide formation.Enzymic syntheses, in yields of 20-30percent, are described of α-D-Galp-(1->3)-α-D-Galp-OMe, β-D-Galp-(1->3)-β-D-Galp-OMe, β-D-Galp-(1->6)-α-D-Galp-OMe, α-D-Manp-(1->2)-α-D-Manp-OMe, α-D-Manp-(1->6)-α-D-Manp-OMe, α-D-Galp-(1->2)-α-D-Galp-OPhNO2-o, α-D-Galp-(1->3)-α-D-Galp-OPhNO2-p, α-D-Manp-(1->2)-α-D-Manp-OPhNO2-p, and α-D-Manp-(1->2)-α-D-Manp-(1->2)-α-D-Manp-OMe.Soluble and immobilised enzymes have been used.
