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2-{2,5-bis(4-methoxyphenyl)-1H-pyrrol-1-yl}pyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1310709-09-1 Structure
  • Basic information

    1. Product Name: 2-{2,5-bis(4-methoxyphenyl)-1H-pyrrol-1-yl}pyrimidine
    2. Synonyms: 2-{2,5-bis(4-methoxyphenyl)-1H-pyrrol-1-yl}pyrimidine
    3. CAS NO:1310709-09-1
    4. Molecular Formula:
    5. Molecular Weight: 357.412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1310709-09-1.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-{2,5-bis(4-methoxyphenyl)-1H-pyrrol-1-yl}pyrimidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-{2,5-bis(4-methoxyphenyl)-1H-pyrrol-1-yl}pyrimidine(1310709-09-1)
    11. EPA Substance Registry System: 2-{2,5-bis(4-methoxyphenyl)-1H-pyrrol-1-yl}pyrimidine(1310709-09-1)
  • 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: 1310709-09-1(Hazardous Substances Data)

1310709-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1310709-09-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,7,0 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1310709-09:
(9*1)+(8*3)+(7*1)+(6*0)+(5*7)+(4*0)+(3*9)+(2*0)+(1*9)=111
111 % 10 = 1
So 1310709-09-1 is a valid CAS Registry Number.

1310709-09-1Downstream Products

1310709-09-1Relevant articles and documents

Ruthenium-catalyzed direct C-H bond arylations of heteroarenes

Ackermann, Lutz,Lygin, Alexander V.

, p. 3332 - 3335 (2011)

Ruthenium-catalyzed C-H bond arylations of indoles, thiophenes, and pyrroles were accomplished in a highly chemo- and site-selective manner through the use of removable directing groups.

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