74774-18-8 Usage
Uses
Used in Organic Chemistry Research:
.beta.-D-gluco-Hexodialdo-1,5-pyranose, 6-hydrate, hexaacetate is used as a key compound in organic chemistry research for its unique structural features and reactivity. Its hexose sugar and aldose nature, along with the pyranose ring structure, make it a valuable building block for the synthesis of complex organic molecules.
Used in Biochemistry Research:
In biochemistry, .beta.-D-gluco-Hexodialdo-1,5-pyranose, 6-hydrate, hexaacetate is employed as a versatile compound for studying the interactions and mechanisms of various biological processes. Its hydrate and hexaacetate properties allow for the exploration of its role in biochemical reactions and its potential as a therapeutic agent.
Used in Pharmaceutical Industry:
.beta.-D-gluco-Hexodialdo-1,5-pyranose, 6-hydrate, hexaacetate is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity make it a promising candidate for the development of new drugs, particularly those targeting carbohydrate-related diseases and conditions.
Used in Material Science:
In the field of material science, .beta.-D-gluco-Hexodialdo-1,5-pyranose, 6-hydrate, hexaacetate is utilized as a component in the development of novel materials with specific properties. Its structural characteristics and ability to form complexes with other molecules contribute to the creation of advanced materials with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 74774-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,7 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74774-18:
(7*7)+(6*4)+(5*7)+(4*7)+(3*4)+(2*1)+(1*8)=158
158 % 10 = 8
So 74774-18-8 is a valid CAS Registry Number.
74774-18-8Relevant academic research and scientific papers
A Mild Procedure for Cleavage of 1,6-Anhydro Sugars
Zottola, Mark,Rao, B. Venkateswara,Fraser-Reid, Bert
, p. 969 - 970 (2007/10/02)
Acetolysis of 1,6-anhydro sugars can be achieved by treatment with acetic anhydride and triethylsilyl trifluoromethanesulphonate at 0 deg C for 5-15 minutes, under which conditions a wide variety of protecting groups are unaffected, and even the trisulphonate is cleaved, albeit in six hours.
Photobromination of Carbohydrate Derivatives. VI. Funcionalization at C6 of 2,3,4-tri-O-acetyl-1,6-anhydro-β-D-glucopyranose
Ferrier, Robert J.,Furneaux, Richard H.
, p. 1025 - 1036 (2007/10/02)
Photobromination of 2,3,4-tri-O-acetyl-1,6-anhydro-β-D-glucopyranose gives the syrupy 6S (exo) bromide in high yield; further reaction leads to secondary bromination at this position.The monobromide reacts with methanol and thiophenol under conditions of kinetic control to give mainly the endo-methoxy and phenylthio derivatives formed by direct nucleophilic displacement, and from the latter the exo-methoxy acetal was obtained by a second nucleophilic substitution.Acetolysis of these compounds can lead to the coresponding exo-6-acetoxy ester or monocyclicproducts formed by opening of the five-membered rings.
