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4-(p-tolyloxy)-6-chloropyriMidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124040-99-9 Structure
  • Basic information

    1. Product Name: 4-(p-tolyloxy)-6-chloropyriMidine
    2. Synonyms: 4-(p-tolyloxy)-6-chloropyriMidine
    3. CAS NO:124040-99-9
    4. Molecular Formula: C11H9ClN2O
    5. Molecular Weight: 220.65
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124040-99-9.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-(p-tolyloxy)-6-chloropyriMidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(p-tolyloxy)-6-chloropyriMidine(124040-99-9)
    11. EPA Substance Registry System: 4-(p-tolyloxy)-6-chloropyriMidine(124040-99-9)
  • 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: 124040-99-9(Hazardous Substances Data)

124040-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124040-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,4 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124040-99:
(8*1)+(7*2)+(6*4)+(5*0)+(4*4)+(3*0)+(2*9)+(1*9)=89
89 % 10 = 9
So 124040-99-9 is a valid CAS Registry Number.

124040-99-9Relevant articles and documents

Design, synthesis and anticonvulsant activity evaluation of 7-substituted -[1,2,4]-triazolo[4,3-f]pyrimidine derivatives

Guan, Li-Ping,Yan, Zheng-Shun,Tong, Guo-Zhong,Qu, You-Le,Sui, Xin,Chang, Yue

, p. 1076 - 1083,8 (2012/12/12)

In this study, a novel series of 7-substituted-[1,2,4]triazolo[4,3-f] pyrimidine derivatives was synthesized as potential anticonvulsant agents. Their anticonvulsant activities were evaluated by the maximal electroshock (MES) test, and their neurotoxiciti

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