4710-95-6 Usage
Description
2-Amino-2-deoxy-D-allopyranose hydrochloride is a chemical compound that belongs to the class of amino sugars. It is a derivative of D-allopyranose, a six-membered sugar molecule, and contains an amino group and a hydrochloride salt, making it a positively charged molecule. 2-Amino-2-deoxy-D-allopyranose hydrochloride has various potential pharmaceutical applications, including as a component in drug development, as a chemical intermediate in organic synthesis, and as a biochemical research tool.
Uses
Used in Pharmaceutical Industry:
2-Amino-2-deoxy-D-allopyranose hydrochloride is used as a component in drug development for its potential therapeutic properties and as a chemical intermediate in organic synthesis to facilitate the creation of new pharmaceutical compounds.
Used in Biochemical Research:
2-Amino-2-deoxy-D-allopyranose hydrochloride is used as a biochemical research tool to study the structure, function, and interactions of amino sugars in biological systems.
It is important to handle and store this compound according to the safety guidelines provided by the manufacturer, as it can be toxic if ingested or inhaled and may cause irritation to the skin and eyes.
Check Digit Verification of cas no
The CAS Registry Mumber 4710-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,1 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4710-95:
(6*4)+(5*7)+(4*1)+(3*0)+(2*9)+(1*5)=86
86 % 10 = 6
So 4710-95-6 is a valid CAS Registry Number.
4710-95-6Relevant articles and documents
Synthesis of N-protected galactosamine building blocks from D-tagatose via the heyns rearrangement
Wrodnigg, Tanja M.,Lundt, Inge,Stuetz, Arnold E.
, p. 33 - 41 (2007/10/03)
N-Acetyl-D-galactosamine (11), a very important naturally occurring building block of oligosaccharides, is easily accessible via the Heyns rearrangement of D-tagatose (3) with benzylamine. The short and efficient synthesis of various differently N-protected D-galactosamine derivatives is reported. Copyright Taylor & Francis Group, LLC.
Synthesis of 2-amino-2-deoxyglycoses and 2-amino-2-deoxyglycosides from glycals
-
, (2008/06/13)
O-acetylated glycals react with ceric ammonium nitrate in the presence of sodium azide to provide, in good yield, O-acetylated 2-azido-2-deoxy glycosyl nitrates. These nitrates can be used to prepare 2-amino-2-deoxy sugars, such as D-galactosamine and lactosamine. The O-acetylated 2-azido-2-deoxy glycosyl nitrates can alternately be converted to O-acetylated 2-azido-2-deoxy glycosyl halides which are useful in the preparation of O-acetylated 2-azido-2-deoxy glycosides, which in turn can be reduced to 2-amino-2-deoxy glycosides. Of particular interest are the syntheses of 2-amino-2-deoxy glycosides which correspond to the terminal units of the antigenic determinant for the human A blood group. Attachment of these glycosides to a solid support provides immunoabsorbents which efficiently and preferentially absorb anti-A antibodies from blood plasma.
