495-75-0 Usage
Description
2,5-Anhydro-D-mannose is a carbohydrate derivative that exists in a mixture of acetal and aldehyde forms. It is a yellow to orange solid and is known for its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
2,5-Anhydro-D-mannose is used as a building block for the synthesis of various biologically active compounds, such as antibiotics, antifungals, and antiviral agents. Its unique structure allows for the development of novel drugs with improved efficacy and reduced side effects.
Used in Chemical Synthesis:
2,5-Anhydro-D-mannose is used as an intermediate in the synthesis of complex carbohydrates and glycoconjugates, which are essential components of many biological systems. Its versatility in chemical reactions makes it a valuable starting material for the production of various bioactive molecules.
Used in Research and Development:
2,5-Anhydro-D-mannose is used as a research tool to study the structure and function of carbohydrates in biological systems. Its unique properties make it an ideal candidate for investigating carbohydrate recognition, binding, and signaling processes.
Used in Food Industry:
2,5-Anhydro-D-mannose can be used as a sweetener in the food industry due to its high sweetness and low caloric content. Its unique properties also make it suitable for use in the development of new food products with enhanced taste and texture.
Used in Cosmetics Industry:
2,5-Anhydro-D-mannose can be used in the development of cosmetics and personal care products due to its moisturizing and skin-conditioning properties. Its unique structure allows for the creation of innovative formulations with improved efficacy and sensory properties.
Check Digit Verification of cas no
The CAS Registry Mumber 495-75-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 495-75:
(5*4)+(4*9)+(3*5)+(2*7)+(1*5)=90
90 % 10 = 0
So 495-75-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O5/c7-1-3-5(9)6(10)4(2-8)11-3/h1,3-6,8-10H,2H2/t3-,4-,5-,6-/m1/s1
495-75-0Relevant articles and documents
Sequential Removal of Monosaccharides from the Reducing End of Oligosaccharides. 2. Fundamental Studies of a Reaction between Hydrazino Compounds and Sugars Having a Glycosyl Moiety on a Carbon Atom Adjacent to a Carbonyl Group
Bendiak, Brad,Salayan, Mary E.,Pantoja, Mario
, p. 8245 - 8256 (2007/10/03)
Hydrazine and certain hydrazino derivatives react with sugars having a glycosidic substituent, where the glycosyl moiety is located on a carbon atom adjecent to an aldehyde or keto group of the aglycon, resulting in cleavage of the glycosidic linkage.The reaction proceeds whether the glycon is of the α or β configuration.The released glycosyl moiety, in the presence of excess hydrazino compound, reacts further to give a hydrazone derivative.Removal of the hydrazone group gives the reducing sugar derived from the glycon.
