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1603836-07-2

4S-{(1R,7S,10R)-8-N-benzyl-3,8-diaza-9-oxa-2-oxobicylo[5,3,0]decan-10-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 4S-{(1R,7S,10R)-8-N-benzyl-3,8-diaza-9-oxa-2-oxobicylo[5,3,0]decan-10-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

    Cas No: 1603836-07-2

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  • 4S-{(1R,7S,10R)-8-N-benzyl-3,8-diaza-9-oxa-2-oxobicylo[5,3,0]decan-10-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose

    Cas No: 1603836-07-2

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  • 1603836-07-2 Structure

  • Basic information

    1. Product Name: 4S-{(1R,7S,10R)-8-N-benzyl-3,8-diaza-9-oxa-2-oxobicylo[5,3,0]decan-10-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose
    2. Synonyms: 4S-{(1R,7S,10R)-8-N-benzyl-3,8-diaza-9-oxa-2-oxobicylo[5,3,0]decan-10-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose
    3. CAS NO:1603836-07-2
    4. Molecular Formula:
    5. Molecular Weight: 686.996
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1603836-07-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4S-{(1R,7S,10R)-8-N-benzyl-3,8-diaza-9-oxa-2-oxobicylo[5,3,0]decan-10-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4S-{(1R,7S,10R)-8-N-benzyl-3,8-diaza-9-oxa-2-oxobicylo[5,3,0]decan-10-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose(1603836-07-2)
    11. EPA Substance Registry System: 4S-{(1R,7S,10R)-8-N-benzyl-3,8-diaza-9-oxa-2-oxobicylo[5,3,0]decan-10-yl}-2,3-di-O-tert-butyldimethylsilyl-1-(uracil-1-yl)-β-D-erythro-furanose(1603836-07-2)

  • 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: 1603836-07-2(Hazardous Substances Data)

1603836-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1603836-07-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,3,8,3 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1603836-07:
(9*1)+(8*6)+(7*0)+(6*3)+(5*8)+(4*3)+(3*6)+(2*0)+(1*7)=152
152 % 10 = 2
So 1603836-07-2 is a valid CAS Registry Number.

1603836-07-2Downstream Products

1603836-07-2Relevant articles and documents

Function-oriented synthesis of liponucleoside antibiotics

Tanino, Tetsuya,Yamaguchi, Mayumi,Matsuda, Akira,Ichikawa, Satoshi

supporting information, p. 1836 - 1840 (2015/10/05)

Function-oriented synthesis of a class of liponucleoside antibiotics was investigated through rational simplification guided by previous structure-activity relationship studies of caprazamycins and muraymycins to address the issue associated with their molecular complexity. A lactam-fused isoxazolidine scaffold was designed, and a diverse set of lactam-fused isoxazolidines derivatives were constructed by intramolecular 1,3-dipolar cycloaddition of alkenyl nitrones. Several analogues exhibited moderate activity against a range of Gram-positive drug-resistant bacterial pathogens. Caprazamycins and muraymycins are rationally simplified to lactam-fused isoxazolidine derivatives by function-oriented synthesis. The designed compounds are synthesized through a domino reaction including nitrone formation and intramolecular 1,3-dipolar cycloaddition. TBS = tert-butyldimethylsilyl.

Function-oriented synthesis of liponucleoside antibiotics

Tanino, Tetsuya,Yamaguchi, Mayumi,Matsuda, Akira,Ichikawa, Satoshi

, p. 1836 - 1840 (2014/04/03)

Function-oriented synthesis of a class of liponucleoside antibiotics was investigated through rational simplification guided by previous structure-activity relationship studies of caprazamycins and muraymycins to address the issue associated with their molecular complexity. A lactam-fused isoxazolidine scaffold was designed, and a diverse set of lactam-fused isoxazolidines derivatives were constructed by intramolecular 1,3-dipolar cycloaddition of alkenyl nitrones. Several analogues exhibited moderate activity against a range of Gram-positive drug-resistant bacterial pathogens.

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