Ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside is a complex chemical compound derived from glucose, featuring an ethyl ester, two benzoyl groups, and a benzylidene group attached to the hydroxyl groups of the sugar molecule. It also contains a thioether functional group, which contributes to its unique chemical properties and potential applications in various fields.
20701-63-7
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Basic information
- Product Name: ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside
- Synonyms: ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside
- CAS NO:20701-63-7
- Molecular Formula:
- Molecular Weight: 520.603
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
- NIST Chemistry Reference: ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside(20701-63-7)
- EPA Substance Registry System: ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside(20701-63-7)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 20701-63-7(Hazardous Substances Data)
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20701-63-7 Usage
Uses
Used in Organic Synthesis:Ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside serves as a versatile intermediate in organic synthesis, particularly for the preparation of complex organic molecules. Its multiple functional groups allow for a range of chemical reactions, making it a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
As a synthetic derivative of glucose, ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside may have potential applications in medicinal chemistry. Its unique structure and functional groups can be exploited for the development of new drugs or drug candidates, particularly in the areas of carbohydrate-based therapeutics and glycobiology.
Used in Chemical Research:
Ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside can also be utilized in chemical research to study the reactivity and properties of various functional groups. Its complex structure provides a platform for investigating the effects of different substituents on the chemical behavior of glucose derivatives, contributing to the understanding of carbohydrate chemistry and its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 20701-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,0 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.Calculate Digit Verification of CAS Registry Number 20701-63:
(7*2)+(6*0)+(5*7)+(4*0)+(3*1)+(2*6)+(1*3)=67
67 % 10 = 7
So 20701-63-7 is a valid CAS Registry Number.
20701-63-7Upstream product
20701-63-7Downstream Products
- 168275-63-6 ethyl 2,3-di-O-benzoyl-4-O-benzyl-1-thio-β-D-glucopyranoside
- 20701-64-8 ethyl 2,3-di-O-benzoyl-1-thio-β-D-glucopyranoside
- 286845-71-4 ethyl 2,3-di-O-benzoyl-4-O-benzyl-6-O-chloroacetyl-1-thio-β-D-glucopyranoside
- 286845-73-6 2-(4-trifluoroacetamidophenyl)ethyl (2,3-di-O-benzoyl-4-O-benzyl-β-D-glucopyranosyl)-(1->4)-6,7-di-O-benzyl-2,3-O-isopropylidene-L-glycero-α-D-manno-heptopyranoside
- 286845-72-5 2-(4-trifluoroacetamidophenyl)ethyl (2,3-di-O-benzoyl-4-O-benzyl-6-O-chloroacetyl-β-D-glucopyranosyl)-(1->4)-6,7-di-O-benzyl-2,3-O-isopropylidene-L-glycero-α-D-manno-heptopyranoside
- 35784-52-2 ethyl 2,3,6-tri-O-benzoyl-1-thio-β-D-glucopyranoside
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ethyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside
