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CAS

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30018-46-3

3-(4-methoxyphenyl)-5-methyl-2-phenyl-1H-pyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30018-46-3 Structure

  • Basic information

    1. Product Name: 3-(4-methoxyphenyl)-5-methyl-2-phenyl-1H-pyrrole
    2. Synonyms: 3-(4-methoxyphenyl)-5-methyl-2-phenyl-1H-pyrrole
    3. CAS NO:30018-46-3
    4. Molecular Formula:
    5. Molecular Weight: 263.339
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30018-46-3.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: 3-(4-methoxyphenyl)-5-methyl-2-phenyl-1H-pyrrole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-methoxyphenyl)-5-methyl-2-phenyl-1H-pyrrole(30018-46-3)
    11. EPA Substance Registry System: 3-(4-methoxyphenyl)-5-methyl-2-phenyl-1H-pyrrole(30018-46-3)

  • 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: 30018-46-3(Hazardous Substances Data)

30018-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30018-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,1 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30018-46:
(7*3)+(6*0)+(5*0)+(4*1)+(3*8)+(2*4)+(1*6)=63
63 % 10 = 3
So 30018-46-3 is a valid CAS Registry Number.

30018-46-3Downstream Products

30018-46-3Relevant articles and documents

Synthesis of 2,2,5-Trisubstituted 2 H-Pyrroles and 2,3,5-Trisubstituted 1 H-Pyrroles by Ligand-Controlled Site-Selective Dearomative C2-Arylation and Direct C3-Arylation

Yamaguchi, Miyuki,Fujiwara, Sakiko,Manabe, Kei

, p. 6972 - 6977 (2019)

Palladium-catalyzed site-selective dearomative C2-arylation of 2,5-diaryl-1H-pyrroles with aryl chlorides was accomplished, and a series of 2,2,5-triaryl-2H-pyrroles were synthesized. In addition, the site selectivity of the reaction was switched by simply changing the ligand, and the direct C3-arylated 2,3,5-triaryl-1H-pyrroles were prepared. The obtained 2,2,5-triaryl-2H-pyrroles could be further transformed into 2,2,5,5-tetraarylpyrrolidines.

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