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1820583-64-9

4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is a complex chemical compound that features a beta-D-glucopyranoside backbone with various functional groups attached. The presence of allyl and benzyl groups provides potential reactivity for further chemical modifications, while the methoxyphenyl and phthalimido groups may confer specific biological activity. 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside has potential applications in organic synthesis, medicinal chemistry, and chemical biology research, with further studies needed to explore its synthetic utility and biological properties.

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  • 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside

    Cas No: 1820583-64-9

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  • 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside

    Cas No: 1820583-64-9

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  • 1820583-64-9 Structure

  • Basic information

    1. Product Name: 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside
    2. Synonyms: 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside
    3. CAS NO:1820583-64-9
    4. Molecular Formula: C31H31NO8
    5. Molecular Weight: 545.58
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1820583-64-9.mol
    9. Article Data: 1

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 707.6±60.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.33±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 12.90±0.70(Predicted)
    10. CAS DataBase Reference: 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside(1820583-64-9)
    12. EPA Substance Registry System: 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside(1820583-64-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1820583-64-9(Hazardous Substances Data)

1820583-64-9 Usage

Uses

Used in Organic Synthesis:
4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is used as a versatile intermediate in organic synthesis for the creation of a variety of complex organic molecules. Its unique structure allows for selective reactions and modifications, making it a valuable building block in the synthesis of pharmaceuticals and other bioactive compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is used as a potential lead compound for the development of new drugs. Its specific functional groups may contribute to its biological activity, and further research could reveal its therapeutic potential in treating various diseases.
Used in Chemical Biology Research:
4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is utilized in chemical biology research as a tool compound to study the interactions between small molecules and biological systems. Its unique structure and potential reactivity make it suitable for probing the mechanisms of biological processes and for the development of targeted therapies.
Used in Pharmaceutical Industry:
4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is used as a key component in the development of novel pharmaceuticals. Its potential reactivity and biological activity make it a promising candidate for the creation of innovative drugs with improved efficacy and selectivity.
Used in Biochemical Research:
In biochemical research, 4-Methoxyphenyl 3-O-Allyl-6-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside is used as a research tool to investigate the binding and interactions of small molecules with biomolecules such as proteins and enzymes. This can help in understanding the molecular basis of diseases and in the design of more effective therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1820583-64-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,2,0,5,8 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1820583-64:
(9*1)+(8*8)+(7*2)+(6*0)+(5*5)+(4*8)+(3*3)+(2*6)+(1*4)=169
169 % 10 = 9
So 1820583-64-9 is a valid CAS Registry Number.

1820583-64-9Upstream product

1820583-64-9Downstream Products

1820583-64-9Relevant articles and documents

Stereoinversion of Stereocongested Carbocyclic Alcohols via Triflylation and Subsequent Treatment with Aqueous N,N-Dimethylformamide

Ochiai, Hidenori,Niwa, Takashi,Hosoya, Takamitsu

supporting information, p. 5982 - 5985 (2016/12/09)

A convenient method for the stereoinversion of secondary alcohols, applicable to stereocongested carbocyclic substrates, is reported. A simple three-step procedure, including triflylation of the hydroxy group, nucleophilic oxygenative displacement by the treatment with aqueous N,N-dimethylformamide (DMF), and methanolysis, allowed for efficient stereoinversion of various substrates, including sugar derivatives, in one pot.

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