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8-ketodeoxycoformycin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69196-03-8 Structure
  • Basic information

    1. Product Name: 8-ketodeoxycoformycin
    2. Synonyms: 8-ketodeoxycoformycin
    3. CAS NO:69196-03-8
    4. Molecular Formula: C11H14N4O4
    5. Molecular Weight: 266.25326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69196-03-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 658.6°C at 760 mmHg
    3. Flash Point: 352.1°C
    4. Appearance: /
    5. Density: 1.8g/cm3
    6. Vapor Pressure: 3.05E-18mmHg at 25°C
    7. Refractive Index: 1.793
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 8-ketodeoxycoformycin(CAS DataBase Reference)
    11. NIST Chemistry Reference: 8-ketodeoxycoformycin(69196-03-8)
    12. EPA Substance Registry System: 8-ketodeoxycoformycin(69196-03-8)
  • 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: 69196-03-8(Hazardous Substances Data)

69196-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69196-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,9 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69196-03:
(7*6)+(6*9)+(5*1)+(4*9)+(3*6)+(2*0)+(1*3)=158
158 % 10 = 8
So 69196-03-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N4O4/c16-3-8-6(17)1-9(19-8)15-5-14-10-7(18)2-12-4-13-11(10)15/h4-6,8-9,16-17H,1-3H2,(H,12,13)/t6-,8+,9-/m0/s1

69196-03-8Relevant articles and documents

METHOD FOR THE SYNTHESIS OF PENTOSTATIN

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Page/Page column 7, (2018/03/28)

The present invention relates to a method for the stereo-selective production of pentostatin comprising an enzymatic transglycosylation reaction between 6,7-dihydroimidazo-[4,5-d]-[1,3]diazepin-8(3H)-one and a 2'-deoxyribonucleoside, followed by an ruthenium-catalyzed asymmetric transfer hydrogenation.

SYNTHESIS AND MANUFACTURE OF PENTOSTATIN AND ITS PRECURSORS, ANALOGS AND DERIVATIVES

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Page/Page column 7, (2008/06/13)

Methods and compositions are provided for efficiently preparing and manufacturing pentostatin. Also provided are novel precursors of pentostatin, pentostatin analogs and derivatives. In one aspect of the invention, a method is provided for total chemical synthesis of pentostatin via a route of heterocyclic ring expansion. For example, a heterocyclic pharmaceutical intermediate for drugs such as pentostatin, e.g., the diazepinone precursor, can be obtained efficiently through a ring expansion of an O-C-N functionality in a hypoxanthine or 2'-deoxyinosine derivative. The methods and compositions can also be used to synthesize and manufacture heterocyclic compounds other than pentostatin, especially pharmaceutically important heterocyclic compounds.

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