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1-O-Benzyloxycarbonyl-4-O,6-O-ethylidene-β-D-glucopyranose, also known as 4,6-O-Ethylidene-α,β-D-glucopyranoside, is a synthetic carbohydrate derivative that serves as a protected form of glucose. 1-O-Benzyloxycarbonyl-4-O,6-O-ethylidene-β-D-glucopyranose is characterized by the presence of a benzyl and ethylidene group attached to the glucose molecule, which allows for selective manipulation and modification at specific positions. It is widely utilized in organic synthesis for the assembly of complex sugar-derived molecules and has potential applications in pharmaceuticals, natural product synthesis, and the study of carbohydrate chemistry.

35901-25-8

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35901-25-8 Usage

Uses

Used in Pharmaceutical Industry:
1-O-Benzyloxycarbonyl-4-O,6-O-ethylidene-β-D-glucopyranose is used as a building block for the synthesis of various pharmaceuticals, due to its unique reactivity and functional properties as a glucose derivative. It enables the development of new drugs with improved therapeutic effects and reduced side effects.
Used in Natural Product Synthesis:
In the field of natural product synthesis, 1-O-Benzyloxycarbonyl-4-O,6-O-ethylidene-β-D-glucopyranose is employed as a key intermediate for the preparation of complex natural products containing sugar moieties. Its selective reactivity allows for the efficient construction of target molecules with desired structural features.
Used in Carbohydrate Chemistry Research:
1-O-Benzyloxycarbonyl-4-O,6-O-ethylidene-β-D-glucopyranose is utilized as a model compound in carbohydrate chemistry research to study the properties and reactivity of sugar derivatives. It provides valuable insights into the fundamental aspects of carbohydrate chemistry and contributes to the development of novel synthetic strategies and methodologies.
Used in Drug Development:
The unique reactivity and functional properties of 1-O-Benzyloxycarbonyl-4-O,6-O-ethylidene-β-D-glucopyranose make it a promising candidate for the development of new drugs and materials. Its potential applications in drug discovery include the design and synthesis of glycoconjugates, glycoproteins, and other bioactive molecules with therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 35901-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,0 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 35901-25:
(7*3)+(6*5)+(5*9)+(4*0)+(3*1)+(2*2)+(1*5)=108
108 % 10 = 8
So 35901-25-8 is a valid CAS Registry Number.

35901-25-8Upstream product

35901-25-8Downstream Products

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