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CAS

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1265166-13-9

1-(4-chlorophenyl)-2,5-dimethyl-N-(p-tolyl)-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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  • 1265166-13-9 Structure

  • Basic information

    1. Product Name: 1-(4-chlorophenyl)-2,5-dimethyl-N-(p-tolyl)-1H-pyrrole-3-carboxamide
    2. Synonyms: 1-(4-chlorophenyl)-2,5-dimethyl-N-(p-tolyl)-1H-pyrrole-3-carboxamide
    3. CAS NO:1265166-13-9
    4. Molecular Formula:
    5. Molecular Weight: 338.837
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1265166-13-9.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: 1-(4-chlorophenyl)-2,5-dimethyl-N-(p-tolyl)-1H-pyrrole-3-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-chlorophenyl)-2,5-dimethyl-N-(p-tolyl)-1H-pyrrole-3-carboxamide(1265166-13-9)
    11. EPA Substance Registry System: 1-(4-chlorophenyl)-2,5-dimethyl-N-(p-tolyl)-1H-pyrrole-3-carboxamide(1265166-13-9)

  • 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: 1265166-13-9(Hazardous Substances Data)

1265166-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1265166-13-9 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 1265166-13:
(9*1)+(8*2)+(7*6)+(6*5)+(5*1)+(4*6)+(3*6)+(2*1)+(1*3)=149
149 % 10 = 9
So 1265166-13-9 is a valid CAS Registry Number.

1265166-13-9Downstream Products

1265166-13-9Relevant articles and documents

Dimethyl sulfoxide participant iron-mediated cascade oxidation/α-formylation reaction of substituted 2,3-dihydropyrroles under air and protonic acid free condition

Zhang, Zhiguo,Tian, Qing,Qian, Jingjing,Liu, Qingfeng,Liu, Tongxin,Shi, Lei,Zhang, Guisheng

, p. 8182 - 8188 (2014)

An efficient and Bronsted acid free one-pot protocol to directly generate structurally sophisticated α-formylpyrrole derivatives in moderate to good yields has been demonstrated, involving an iron-mediated domino oxidation/formylation reaction of readily available 2,3-dihydro-1H-pyrroles in dimethyl sulfoxide and air atmosphere, in which dimethyl sulfoxide acts as the formyl donor. A possible mechanism is presented.

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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