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CAS

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1030380-50-7

4,6-bis(3,5-dichlorophenyl)-2-methylpyrimidine, commonly known as BDCM, is a synthetic organic compound characterized by a pyrimidine base structure. It is recognized for its selective activity against specific plant and insect species, which makes it a favored option for targeted pest management in agricultural and industrial applications.

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  • 1030380-50-7 Structure

  • Basic information

    1. Product Name: 4,6-bis(3,5-dichlorophenyl)-2-methylpyrimidine
    2. Synonyms: 4,6-bis(3,5-dichlorophenyl)-2-methylpyrimidine
    3. CAS NO:1030380-50-7
    4. Molecular Formula:
    5. Molecular Weight: 384.092
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1030380-50-7.mol

  • Chemical Properties

    1. Melting Point: 230-231 °C(Solv: toluene (108-88-3))
    2. Boiling Point: 508.3±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.419±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4,6-bis(3,5-dichlorophenyl)-2-methylpyrimidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,6-bis(3,5-dichlorophenyl)-2-methylpyrimidine(1030380-50-7)
    11. EPA Substance Registry System: 4,6-bis(3,5-dichlorophenyl)-2-methylpyrimidine(1030380-50-7)

  • 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: 1030380-50-7(Hazardous Substances Data)

1030380-50-7 Usage

Uses

Used in Agricultural Industry:
BDCM is utilized as a pesticide and herbicide for controlling a variety of weeds and pests. Its selective activity allows for effective targeted pest management, enhancing crop protection and yield.
Used in Industrial Settings:
In industrial applications, BDCM serves a similar purpose in managing unwanted plant growth and pests, particularly in areas where such infestations could impact infrastructure or pose safety risks.
However, due to its potential environmental and health impacts, BDCM has been subject to regulatory scrutiny. It is known to persist in soil and water, which can pose risks to aquatic organisms and potentially enter the food chain. Human exposure to BDCM has been associated with adverse effects such as skin and eye irritation, respiratory issues, and potential carcinogenicity. Consequently, regulatory limits and guidelines have been established to mitigate these risks and ensure the safe and responsible use of BDCM in relevant industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1030380-50-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,3,8 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1030380-50:
(9*1)+(8*0)+(7*3)+(6*0)+(5*3)+(4*8)+(3*0)+(2*5)+(1*0)=87
87 % 10 = 7
So 1030380-50-7 is a valid CAS Registry Number.

1030380-50-7Relevant articles and documents

Influence of substituted pyridine rings on physical properties and electron mobilities of 2-methylpyrimidine skeleton-based electron transporters

Sasabe, Hisahiro,Tanaka, Daisaku,Yokoyama, Daisuke,Chiba, Takayuki,Pu, Yong-Jin,Nakayama, Ken-Ichi,Yokoyama, Masaaki,Kido, Junji

experimental part, p. 336 - 342 (2011/12/15)

A series of 2-methylpyrimidine skeleton-based electron-transporting derivatives (BPyMPM) are designed and synthesized to investigate the influence of substituted pyridine rings on the physical properties and electron mobilities (μe). The only structural difference is the position of substituted pyridine rings. The melting point (Tm) of B4PyMPM is estimated to be ca. 50 °C higher than that of B3PyMPM, and ca. 120 °C higher than that of B2PyMPM. The ionization potential is observed to increase in the order B2PyMPM (6.62 eV) e at 298 K of B4PyMPM is 10 times higher than that of B3PyMPM and 100 times higher than that of B2PyMPM. To extract the charge transport parameters, the temperature and field dependencies of μe are investigated. Using Baessler's disorder formalism, the degree of energetic disorder is estimated to decrease in the order B2PyMPM (91 meV) > B3PyMPM (88 meV) > B4PyMPM (76 meV), and the positional disorder is 2.7 for B2PyMPM, and e) of 2-methylpyrimidine skeleton-based electron-transporters is investigated. Although the structural difference is very small, the difference in μe is found to be quite large. At 298 K, the μe of B4PyMPM is measured to be 10 times higher than that of B3PyMPM and 100 times higher than that of B2PyMPM. Copyright

Palladium-catalyzed cross-coupling reaction of 2- and/or 5-substituted 4,6-dichloropyrimidines with arylboronic acids

Tumkevicius,Dodonova,Baskirova,Voitechovicius

experimental part, p. 960 - 964 (2009/12/06)

(Chemical Equation Presented) The Suzuki-Miyaura reaction of some 4,6-dichloropyrimidines bearing methylthio-, methyl-, amino-, cyano-, formyl-, and nitro groups in positions 2 and/or 5 of the pyrimidine ring with arylboronic acids has been investigated. Influence of palladium catalyst, ligand, base, and solvent on the reaction outcome was studied. The reaction was found to give the corresponding 4,6-diarylpyrimidines in reasonable yields using Pd(OAc) 2/PPh3/K3PO4 or Pd(PPh 3)2Cl2/K3PO4 as catalyst systems.

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