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CAS

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923568-64-3

1-[5-O-benzoyl-2,3-dideoxy-3,4-C-(difluoromethylene)-β-D-erythro-pentofuranosyl]uracil is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 923568-64-3 Structure

  • Basic information

    1. Product Name: 1-[5-O-benzoyl-2,3-dideoxy-3,4-C-(difluoromethylene)-β-D-erythro-pentofuranosyl]uracil
    2. Synonyms: 1-[5-O-benzoyl-2,3-dideoxy-3,4-C-(difluoromethylene)-β-D-erythro-pentofuranosyl]uracil
    3. CAS NO:923568-64-3
    4. Molecular Formula:
    5. Molecular Weight: 364.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 923568-64-3.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: 1-[5-O-benzoyl-2,3-dideoxy-3,4-C-(difluoromethylene)-β-D-erythro-pentofuranosyl]uracil(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[5-O-benzoyl-2,3-dideoxy-3,4-C-(difluoromethylene)-β-D-erythro-pentofuranosyl]uracil(923568-64-3)
    11. EPA Substance Registry System: 1-[5-O-benzoyl-2,3-dideoxy-3,4-C-(difluoromethylene)-β-D-erythro-pentofuranosyl]uracil(923568-64-3)

  • 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: 923568-64-3(Hazardous Substances Data)

923568-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923568-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,5,6 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 923568-64:
(8*9)+(7*2)+(6*3)+(5*5)+(4*6)+(3*8)+(2*6)+(1*4)=193
193 % 10 = 3
So 923568-64-3 is a valid CAS Registry Number.

923568-64-3Relevant articles and documents

Addition of difluorocarbene to 3′,4′-unsaturated nucleosides: Synthesis of 2′-deoxy analogues with a 2-oxabicyclo[3.1.0]hexane framework

Nowak, Ireneusz,Cannon, John F.,Robins, Morris J.

, p. 532 - 537 (2007/10/03)

Treatment of protected 2′-deoxy-3′,4′-unsaturated nucleosides derived from adenosine and uridine with difluorocarbene [generated from bis(trifluoromethyl)mercury and sodium iodide] gave fused-ring 2,2-difluorocyclopropane compounds. Stereoselective α-face

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