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4,6-Di(4-carboxyphenyl)pyrimidine is a pyrimidine derivative with the molecular formula C18H10N4O4. It features a pyrimidine ring with two carboxyphenyl groups attached at the 4 and 6 positions, endowing it with unique electron-accepting properties and the capacity to form stable complexes with metal ions. This chemical compound holds promise for a variety of applications in materials science, organic electronics, and as a building block in the synthesis of organic compounds for pharmaceuticals and agrochemicals.

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  • 609356-00-5 Structure
  • Basic information

    1. Product Name: 4,6-Di(4-carboxyphenyl)pyrimidine
    2. Synonyms: 4,4'-(Pyrimidine-4,6-diyl)dibenzoic acid;Benzoic acid, 4,4'-(4,6-pyrimidinediyl)bis-
    3. CAS NO:609356-00-5
    4. Molecular Formula: C18H12N2O4
    5. Molecular Weight: 320.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 609356-00-5.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: 4,6-Di(4-carboxyphenyl)pyrimidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,6-Di(4-carboxyphenyl)pyrimidine(609356-00-5)
    11. EPA Substance Registry System: 4,6-Di(4-carboxyphenyl)pyrimidine(609356-00-5)
  • 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: 609356-00-5(Hazardous Substances Data)

609356-00-5 Usage

Uses

Used in Materials Science:
4,6-Di(4-carboxyphenyl)pyrimidine is used as a component in the development of advanced materials due to its electron-accepting properties, which can enhance the performance of materials in various applications.
Used in Organic Electronics:
In the field of organic electronics, 4,6-Di(4-carboxyphenyl)pyrimidine is utilized as a key component in the design of organic semiconductors, taking advantage of its ability to form stable complexes with metal ions, which can improve the efficiency and stability of electronic devices.
Used in Pharmaceutical Synthesis:
4,6-Di(4-carboxyphenyl)pyrimidine serves as a building block in the synthesis of organic compounds for pharmaceuticals, potentially contributing to the development of new drugs with novel therapeutic properties.
Used in Agrochemical Synthesis:
Similarly, in agrochemicals, 4,6-Di(4-carboxyphenyl)pyrimidine is used as a precursor in the synthesis of organic compounds, which may lead to the creation of innovative agrochemicals with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 609356-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,9,3,5 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 609356-00:
(8*6)+(7*0)+(6*9)+(5*3)+(4*5)+(3*6)+(2*0)+(1*0)=155
155 % 10 = 5
So 609356-00-5 is a valid CAS Registry Number.

609356-00-5Downstream Products

609356-00-5Relevant articles and documents

Design, synthesis, and evaluation of novel biarylpyrimidines: A new class of ligand for unusual nucleic acid structures

Wheelhouse, Richard T.,Jennings, Sharon A.,Phillips, Victoria A.,Pletsas, Dimitrios,Murphy, Peter M.,Garbett, Nichola C.,Chaires, Jonathan B.,Jenkins, Terence C.

, p. 5187 - 5198 (2008/04/18)

Biarylpyrimidines are characterized as selective ligands for higher-order nucleic acid structures. A concise and efficient synthesis has been devised incorporating Suzuki biaryl cross-coupling of dihalopyrimidines. Two ligand series are described based on

Biarylpyrimidines: a new class of ligand for high-order DNA recognition.

Murphy, Peter M,Phillips, Victoria A,Jennings, Sharon A,Garbett, Nichola C,Chaires, Jonathan B,Jenkins, Terence C,Wheelhouse, Richard T

, p. 1160 - 1161 (2007/10/03)

Biarylpyrimidines bearing omega-aminoalkyl substituents have been designed as ligands for high-order DNA structures: spectrophotometric, thermal and competition equilibrium dialysis assays showed that changing the functional group for substituent attachme

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