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250727-44-7

1-(3,5-dideoxy-3-phenylthio-β-D-threo-pent-4-enofuranosyl)uracil is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 250727-44-7 Structure

  • Basic information

    1. Product Name: 1-(3,5-dideoxy-3-phenylthio-β-D-threo-pent-4-enofuranosyl)uracil
    2. Synonyms: 1-(3,5-dideoxy-3-phenylthio-β-D-threo-pent-4-enofuranosyl)uracil
    3. CAS NO:250727-44-7
    4. Molecular Formula:
    5. Molecular Weight: 318.353
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 250727-44-7.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-(3,5-dideoxy-3-phenylthio-β-D-threo-pent-4-enofuranosyl)uracil(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(3,5-dideoxy-3-phenylthio-β-D-threo-pent-4-enofuranosyl)uracil(250727-44-7)
    11. EPA Substance Registry System: 1-(3,5-dideoxy-3-phenylthio-β-D-threo-pent-4-enofuranosyl)uracil(250727-44-7)

  • 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: 250727-44-7(Hazardous Substances Data)

250727-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 250727-44-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,7,2 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 250727-44:
(8*2)+(7*5)+(6*0)+(5*7)+(4*2)+(3*7)+(2*4)+(1*4)=127
127 % 10 = 7
So 250727-44-7 is a valid CAS Registry Number.

250727-44-7Downstream Products

250727-44-7Relevant articles and documents

Regioselective modification of the sugar moiety in pyrimidine nucleosides via a 4',5'-dehydro-2',3'-anhydrouridine intermediate

Hirota, Kosaku,Takasu, Hideki,Tsuji, Yoshie,Sajiki, Hironao

, p. 1827 - 1828 (1999)

3'-Substituted pyrimidine nucleoside derivatives are obtained in moderate to high yields by the reaction of 1-(2',3'-anhydro-5'-deoxy -4',5'-didehydro-α-L-erythro-pentofuranosyl)uracil with nucleophiles without the formation of the corresponding 2'-adduct

3′-Selective modification of a 4′,5′-didehydro-5′- deoxy-2′,3′-epoxyuridine using nucleophiles

Takasu, Hideki,Tsuji, Yoshie,Sajiki, Hironao,Hirota, Kosaku

, p. 8499 - 8504 (2005)

1-(2,3-Anhydro-5-deoxy-4,5-didehydro-α-l-erythro-pent-4-enofuranosyl) uracil 4 was obtained by the treatment of 5′-iodo-2′,3′- epoxyuridine 5 with LiHMDS in excellent yield. The pyrimidine nucleoside 4 possesses quite unique vinyl epoxide moiety within th

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