532-19-4 Usage
Description
2-Amino-2-deoxy-D-ribose, also known as Ribosamine, is a monosaccharide derived from the sugar ribose. It is an essential component in the biosynthesis of various biological molecules, including nucleic acids and glycoproteins. Its unique structure allows it to participate in a wide range of biochemical reactions and applications across different industries.
Uses
Used in Pharmaceutical Industry:
2-Amino-2-deoxy-D-ribose is used as a key intermediate for the synthesis of various biologically active compounds, such as 6-deoxy-L-talose and 2-amino-2,6-dideoxy-L-talose. These compounds have potential applications in the development of new drugs and therapies.
Used in Biochemical Research:
Ribosamine is used as a tool for isolating lectins, which are proteins that can bind to specific sugar molecules. This application is crucial in understanding the interactions between sugars and proteins, which play a significant role in various biological processes.
Used in Glycoprotein Preparation:
2-Amino-2-deoxy-D-ribose is also used in the preparation of N-glycoproteins, which are proteins with attached sugar molecules. These glycoproteins are essential for various cellular functions, including cell signaling, immune response, and cell adhesion. The use of Ribosamine in their preparation aids in the study and development of therapeutic strategies targeting glycoprotein-related diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 532-19-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 532-19:
(5*5)+(4*3)+(3*2)+(2*1)+(1*9)=54
54 % 10 = 4
So 532-19-4 is a valid CAS Registry Number.
532-19-4Relevant articles and documents
Process for the preparation of cyclopropane carboxylic acid esters
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, (2008/06/13)
3-(Halogenovinyl- or propenyl-)-2,2-dimethyl cyclopropane-1-carboxylic acid esters, which are precursors of, or may themselves be, pyrethroid insecticides, are prepared by the reaction of certain halogenopentadienes with an alkyl diazoacetate in the presence of a catalyst which is a transition metal complex of certain chiral Schiff bases, which catalysts tend to increase the yield of preferred cis IR isomer relative to the other possible isomers.
