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2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL is a carbohydrate chemical compound that is a derivative of D-mannitol. It features a distinctive pyrimidinyl ring structure, which contributes to its unique properties and potential applications.
Used in Pharmaceutical Industry:
2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL is used as a key component in the development of antiviral drugs due to its molecular structure and properties that make it a promising candidate for medicinal chemistry research and development.

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  • 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL

    Cas No: 302790-82-5

  • USD $ 1.9-2.9 / Gram

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  • 302790-82-5 Structure
  • Basic information

    1. Product Name: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL
    2. Synonyms: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL
    3. CAS NO:302790-82-5
    4. Molecular Formula: C10H14N2O6
    5. Molecular Weight: 258.229
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 302790-82-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL(302790-82-5)
    11. EPA Substance Registry System: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL(302790-82-5)
  • 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: 302790-82-5(Hazardous Substances Data)

302790-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302790-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,7,9 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 302790-82:
(8*3)+(7*0)+(6*2)+(5*7)+(4*9)+(3*0)+(2*8)+(1*2)=125
125 % 10 = 5
So 302790-82-5 is a valid CAS Registry Number.

302790-82-5Downstream Products

302790-82-5Relevant articles and documents

Synthesis of 3-deoxy-3-nucleobase-2,5-anhydro-D-mannitol: A novel class of hydroxymethyl-branched isonucleosides

Lei,Min,Zhang

, p. 2899 - 2906 (2007/10/03)

A concise synthesis of 3-deoxy-3-nucleobase-2,5-anhydro-D-mannitol 6(a- d) has been achieved, using the deamination of 2-amino-2-deoxy-D-glucose to construct in one step the sugar skeleton with the desired sense of chirality at each asymmetric center. The selective dibenzoylation of 2,5-anhydro-D- mannitol 9 was investigated, and the key epoxide intermediate 13 was obtained in good yield via an intramolecular Mitsunobu reaction. The process of opening of epoxide 13 by nucleobases appeared to be regioselective. (C) 2000 Elsevier Science Ltd.

Stereoselective synthesis of 4-deoxy-4-nucleobase-2,5-anhydro-L-mannitol derivatives

Yang,Yu,Min,Ma,Zhang

, p. 2739 - 2747 (2007/10/03)

2,5:3,4-Dianhydro-L-talofuranose dimethylacetal 7 was synthesized from D-glucose in 7 steps. A series of 4-deoxy-4-nucleobase-2,5-anhydro-L-mannitols 13-16 were synthesized regioselectively from 7 in good yields. 6-O-p-Tolylsulfonyl-2,5:3,4-dianhydro-L-ta

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