24516-44-7 Usage
Chemical compound
A substance formed from the dehydration of glucose, resulting in the elimination of the hydroxyl group on carbon atom 1.
Cyclic form
The compound exists as a cyclic structure, with a double bond between carbon atoms 1 and 4.
Natural occurrence
Found in various natural polymers and polysaccharides, playing a significant role in the formation of glycosidic bonds in carbohydrates.
Pharmaceutical synthesis
Used in the synthesis of pharmaceuticals and various other organic compounds.
Advanced materials and biomaterials
Has potential applications in the development of advanced materials and biomaterials due to its unique chemical and structural properties.
Molecular weight
The molecular weight of 1,4-Anhydro-β-D-glucopyranose is approximately 162.14 g/mol.
Solubility
The compound is generally soluble in water and some organic solvents, such as methanol and ethanol.
Melting point
The melting point of 1,4-Anhydro-β-D-glucopyranose is around 132-134°C.
Optical activity
As a chiral compound, 1,4-Anhydro-β-D-glucopyranose exhibits optical activity, meaning it can rotate plane-polarized light.
Check Digit Verification of cas no
The CAS Registry Mumber 24516-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,1 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24516-44:
(7*2)+(6*4)+(5*5)+(4*1)+(3*6)+(2*4)+(1*4)=97
97 % 10 = 7
So 24516-44-7 is a valid CAS Registry Number.
24516-44-7Relevant academic research and scientific papers
The UDP-Galp mutase catalyzed isomerization: Synthesis and evaluation of 1,4-anhydro-β-d-galactopyranose and its [2.2.2] methylene homologue
Sadeghi-Khomami, Ali,Forcada, Tatiana J.,Wilson, Claire,Sanders, David A. R.,Thomas, Neil R.
experimental part, p. 1596 - 1602 (2010/07/04)
The synthesis of 1,4-anhydro-β-d-galactopyranose (1,5-anhydro-α- d-galactofuranose), a proposed intermediate in the ring contraction isomerisation catalyzed by UDP-galactopyranose mutase, together with its [2.2.2] bicyclic methylene homologue, synthesised as a possible competitive inhibitor or alternative substrate, are reported. Neither compound was found to be an inhibitor or substrate for UDP-galactopyranose mutase from Klebsiella pneumoniae.
1,4-Anhydrogalactopyranose is not an intermediate of the mutase catalyzed UDP-galactopyranose/furanose interconversion
Caravano, Audrey,Sinay, Pierre,Vincent, Stephane P.
, p. 1123 - 1125 (2007/10/03)
UDP-galactopyranose mutase (UGM) catalyzes the isomerization of UDP-galactopyranose (UDP-Galp) into UDP-galactofuranose (UDP-Galf), an essential step of the mycobacterial cell wall biosynthesis. The first mechanistic assumption proposed in the literature
