70835-78-8 Usage
Uses
Used in Organic Chemistry:
2,3:4,6-Di-o-cyclohexylidene-α-D-mannopyranose is used as a synthetic intermediate for the preparation of various complex organic compounds. Its unique structure allows for selective reactions and the formation of diverse products, making it a valuable building block in organic synthesis.
Used in Carbohydrate Chemistry:
In the field of carbohydrate chemistry, 2,3:4,6-Di-o-cyclohexylidene-α-D-mannopyranose is used for the synthesis of α-mannosides. The presence of the cyclohexylidene groups enhances the reactivity of the molecule, facilitating the formation of glycosidic linkages with various aglycones. This allows for the preparation of a wide range of α-mannosides with potential applications in various fields.
Used in Pharmaceutical Industry:
2,3:4,6-Di-o-cyclohexylidene-α-D-mannopyranose is also used for the synthesis of β-mannosides, which are important in the development of pharmaceutical compounds. The ability to selectively synthesize β-mannosides can lead to the discovery of new drugs with improved properties, such as enhanced stability, bioavailability, and therapeutic efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 70835-78-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,3 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70835-78:
(7*7)+(6*0)+(5*8)+(4*3)+(3*5)+(2*7)+(1*8)=138
138 % 10 = 8
So 70835-78-8 is a valid CAS Registry Number.
70835-78-8Relevant academic research and scientific papers
Synthesis of new UV-B light absorbents: (Acetylphenyl)glycosides with antioxidant activities
Otani, Takashi,Tsubogo, Tetsu,Furukawa, Naoki,Saito, Takao,Uchida, Katsumi,Iwama, Kanako,Kanai, Yuki,Yajima, Hirofumi
scheme or table, p. 3582 - 3584 (2009/04/04)
m-Acetylphenyl-β-d-glucopyranosides and m-acetylphenyl-α/β-d-mannopyranosides were synthesized by the Koenigs-Knorr, Mitsunobu, and Helferich reactions as key glycosylation reactions, respectively. Their spectroscopic properties and antioxidative activities were characterized as potential ultraviolet B-ray absorbents.
