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1265166-16-2

N,1-bis(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1265166-16-2 Structure

  • Basic information

    1. Product Name: N,1-bis(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3-carboxamide
    2. Synonyms: N,1-bis(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3-carboxamide
    3. CAS NO:1265166-16-2
    4. Molecular Formula:
    5. Molecular Weight: 359.255
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1265166-16-2.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: N,1-bis(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,1-bis(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3-carboxamide(1265166-16-2)
    11. EPA Substance Registry System: N,1-bis(4-chlorophenyl)-2,5-dimethyl-1H-pyrrole-3-carboxamide(1265166-16-2)

  • 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: 1265166-16-2(Hazardous Substances Data)

1265166-16-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1265166-16-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,5,1,6 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1265166-16:
(9*1)+(8*2)+(7*6)+(6*5)+(5*1)+(4*6)+(3*6)+(2*1)+(1*6)=152
152 % 10 = 2
So 1265166-16-2 is a valid CAS Registry Number.

1265166-16-2Downstream Products

1265166-16-2Relevant articles and documents

Synthesis of multisubstituted pyrroles from doubly activated cyclopropanes using an iron-mediated oxidation domino reaction

Zhang, Zhiguo,Zhang, Wei,Li, Junlong,Liu, Qingfeng,Liu, Tongxin,Zhang, Guisheng

, p. 11226 - 11233 (2014)

An alternative route has been developed for the construction of multisubstituted pyrrole derivatives from readily available, doubly activated cyclopropanes and anilines using an iron-mediated oxidation domino reaction (i.e., sequential ring-opening, cyclization, and dehydrogenation reactions). This reaction uses readily available reactants and is tolerant of a broad range of substrates, with the desired products being formed in good to excellent yields.

Iron-catalyzed synthesis of polysubstituted pyrroles via [4C+1N] cyclization of 4-acetylenic ketones with primary amines

Wang, Yeming,Bi, Xihe,Li, Dehua,Liao, Peiqiu,Wang, Yidong,Yang, Jin,Zhang, Qian,Liu, Qun

supporting information; experimental part, p. 809 - 811 (2011/04/15)

A highly efficient iron-catalyzed approach to polysubstituted pyrroles has been developed through the [4C+1N] cyclization of 4-acetylenic ketones with primary amines, leading to the synthesis of a variety of tetra- and fully-substituted pyrroles as well a

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