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225232-08-6

2,4-dichloro-6-(3,5-dimethylbenzyl)-5-ethylpyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 225232-08-6 Structure

  • Basic information

    1. Product Name: 2,4-dichloro-6-(3,5-dimethylbenzyl)-5-ethylpyrimidine
    2. Synonyms: 2,4-dichloro-6-(3,5-dimethylbenzyl)-5-ethylpyrimidine
    3. CAS NO:225232-08-6
    4. Molecular Formula:
    5. Molecular Weight: 295.211
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 225232-08-6.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-dichloro-6-(3,5-dimethylbenzyl)-5-ethylpyrimidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-dichloro-6-(3,5-dimethylbenzyl)-5-ethylpyrimidine(225232-08-6)
    11. EPA Substance Registry System: 2,4-dichloro-6-(3,5-dimethylbenzyl)-5-ethylpyrimidine(225232-08-6)

  • 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: 225232-08-6(Hazardous Substances Data)

225232-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 225232-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,2,3 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 225232-08:
(8*2)+(7*2)+(6*5)+(5*2)+(4*3)+(3*2)+(2*0)+(1*8)=96
96 % 10 = 6
So 225232-08-6 is a valid CAS Registry Number.

225232-08-6Relevant articles and documents

Regioselective alkylation and arylation at the 6-position of pyrimidine: Synthesis of 5-alkyl-6-arylmethyl-2,4-pyrimidinediones

Lee, Yeon Soo,Kim, Yong Hae

, p. 1503 - 1517 (1999)

5-Alkyl-2,4,6-trichloropyrimidines reacted with various nucleophiles to afford the regioselectivity 6-substituted pyrimidines as the major products in good yields, which were transformed to 5-alkyl-6-arylmethyl-2,4- pyrimidinediones of a key intermediate

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