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CAS

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903572-19-0

2,4(1H,3H)-Pyrimidinedione, 1-(2,4-dinitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 903572-19-0 Structure

  • Basic information

    1. Product Name: 2,4(1H,3H)-Pyrimidinedione, 1-(2,4-dinitrophenyl)-
    2. Synonyms:
    3. CAS NO:903572-19-0
    4. Molecular Formula: C10H6N4O6
    5. Molecular Weight: 278.181
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 903572-19-0.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: 2,4(1H,3H)-Pyrimidinedione, 1-(2,4-dinitrophenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4(1H,3H)-Pyrimidinedione, 1-(2,4-dinitrophenyl)-(903572-19-0)
    11. EPA Substance Registry System: 2,4(1H,3H)-Pyrimidinedione, 1-(2,4-dinitrophenyl)-(903572-19-0)

  • 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: 903572-19-0(Hazardous Substances Data)

903572-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 903572-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,3,5,7 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 903572-19:
(8*9)+(7*0)+(6*3)+(5*5)+(4*7)+(3*2)+(2*1)+(1*9)=160
160 % 10 = 0
So 903572-19-0 is a valid CAS Registry Number.

903572-19-0Relevant articles and documents

A highly efficient protocol for the synthesis of N-aryl nucleobases using zinc oxide in ionic liquids

Zare,Hasaninejad,Khalafi-Nezhad,Moosavi-Zare,Beyzavi,Khedri,Asadi,Hayati,Asifi

experimental part, p. 461 - 469 (2010/08/20)

A highly efficient and simple method for the synthesis of N-aryl derivatives of pyrimidine and purine nucleobases via N-arylation of nucleobases using zinc oxide in 1-butyl-3-methylimidazolium bromide ([bmim]Br) under microwave as well as thermal conditio

New approach for the synthesis of 1-aryl- and 1-heteroaryl-5-nitrouracil derivatives

Gondela, Andrzej,Walczak, Krzysztof

, p. 2859 - 2864 (2007/10/03)

1-(2,4-Dinitrophenyl)-5-nitrouracil and its 3-methyl derivatives were synthesized and used as substrates in reaction with aromatic amines and amino pyridines. In the reaction of aniline with 1-(2,4-dinitrophenyl)-5-nitrouracil, only the acyclic adduct was isolated. When 1-(2,4-dinitrophenyl)-3-methyl-5-nitrouracil was treated with aniline and other aromatic amines or amino pyridines, the desired 1-aryl-5-nitrouracil derivatives were obtained in satisfactory yield. The influence of the free H-3 proton present in the uracil ring on the course of the reaction is discussed.

Microwave-assisted N-nitroarylation of some pyrimidine and purine nucleobases

Khalafi-Nezhad, Ali,Zare, Abdolkarim,Parhami, Abolfath,Rad Soltani, Mohammad Navid,Nejabat, Gholam Reza

, p. 979 - 985 (2007/10/03)

An efficient procedure for the synthesis of some N-nitroaryl derivatives of nucleobases via microwave-assisted N-nitroarylation of nucleobases in the presence of SiO2 and Cs2CO3 in DMSO, as the homogenizing solvent, is des

Regioselective N-arylation of some pyrimidine and purine nucleobases

Khalafi-Nezhad, Ali,Zare, Abdolkarim,Parhami, Abolfath,Soltani Rad, Mohammad Navid,Nejabat, Gholam Reza

, p. 3549 - 3562 (2007/10/03)

N-Arylation of some pyrimidine and purine nucleobases in the presence of SiO2 and Cs2CO3 under solvent-free as well as in solution conditions is described. In these conditions, N1-aryl pyrimidines and N9-aryl purines have

A convenient method for N-1 arylation of uracil derivatives

Gondela, Andrzej,Walczak, Krzysztof

, p. 4653 - 4657 (2007/10/03)

1-(4-Nitrophenyl)- and 1-(2,4-dinitrophenyl)uracil derivatives have been obtained by direct arylation of uracil and its 5-substituted derivatives using 1-fluoro-4-nitrobenzene or 1-fluoro-2,4-dinitrobenzene in the presence of a base. The application of the newly obtained uracil derivatives in further synthesis is also presented.

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