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114611-82-4

2-Amino-5-((2S,5S)-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114611-82-4 Structure

  • Basic information

    1. Product Name: 2-Amino-5-((2S,5S)-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-4-one
    2. Synonyms:
    3. CAS NO:114611-82-4
    4. Molecular Formula:
    5. Molecular Weight: 211.221
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114611-82-4.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: 2-Amino-5-((2S,5S)-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Amino-5-((2S,5S)-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-4-one(114611-82-4)
    11. EPA Substance Registry System: 2-Amino-5-((2S,5S)-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-4-one(114611-82-4)

  • 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: 114611-82-4(Hazardous Substances Data)

114611-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114611-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,6,1 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114611-82:
(8*1)+(7*1)+(6*4)+(5*6)+(4*1)+(3*1)+(2*8)+(1*2)=94
94 % 10 = 4
So 114611-82-4 is a valid CAS Registry Number.

114611-82-4Downstream Products

114611-82-4Relevant articles and documents

Synthesis of C-Nucleoside Analogues of 2',3'-Dideoxycytidine, 3'-Azido-2',3'-dideoxyuridine (CS-87), and 2',3'-Dideoxy-2',3'-didehydrocytidine

Doboszewski, B.,Chu, C. K.,Halbeek, H. van

, p. 2777 - 2782 (1988)

C-Nucleoside analogues of 2',3'-dideoxycytidine, 3'-azido-2',3'-dideoxyuridine (CS-87), and 2',3'-dideoxy-2',3'-didehydrocytidine were synthesized from pseudouridine.The C-nucleoside analogue of 2',3'-dideoxycytidine 4a was prepared by stepwise deoxygenation of 1,3-dimethylpseudouridine (11a) followed by the ring transformation of the uracil to the isocytosine ring.Reduction of the dimethylxanthate 11c to 2',3'-unsaturated derivative 13 followed by the ring transformation reaction afforded the C-nucleoside analogue of 2',3'-dideoxy-2',3'-didehydrocytidine (5).Finally, the C-nucleoside analogue of 3'-azido-2',3'-dideoxyuridine (CS-87, 6) was prepared from 2'-deoxypseudouridine (22a) as the intermediate, in which the 3'-OH was oxidized to a 3'-keto moiety followed by reduction to yield 25a.Mesylation and displacement of the mesyl group of 25a by the azide moiety followed by deblocking of the silyl protecting group yielded the desired compound 6

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