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169464-88-4

(4-fluorophenyl)(1-methyl-1H-pyrrol-2-yl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 169464-88-4 Structure

  • Basic information

    1. Product Name: (4-fluorophenyl)(1-methyl-1H-pyrrol-2-yl)methanone
    2. Synonyms: (4-fluorophenyl)(1-methyl-1H-pyrrol-2-yl)methanone
    3. CAS NO:169464-88-4
    4. Molecular Formula:
    5. Molecular Weight: 203.216
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 169464-88-4.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: (4-fluorophenyl)(1-methyl-1H-pyrrol-2-yl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-fluorophenyl)(1-methyl-1H-pyrrol-2-yl)methanone(169464-88-4)
    11. EPA Substance Registry System: (4-fluorophenyl)(1-methyl-1H-pyrrol-2-yl)methanone(169464-88-4)

  • 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: 169464-88-4(Hazardous Substances Data)

169464-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169464-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,4,6 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 169464-88:
(8*1)+(7*6)+(6*9)+(5*4)+(4*6)+(3*4)+(2*8)+(1*8)=184
184 % 10 = 4
So 169464-88-4 is a valid CAS Registry Number.

169464-88-4Downstream Products

169464-88-4Relevant articles and documents

An Electrophilic Approach to the Palladium-Catalyzed Carbonylative C-H Functionalization of Heterocycles

Tjutrins, Jevgenijs,Arndtsen, Bruce A.

, p. 12050 - 12054 (2015)

A palladium-catalyzed approach to intermolecular carbonylative C-H functionalization is described. This transformation is mediated by PtBu3-coordinated palladium catalyst and allows the derivatization of a diverse range of heterocycles, including pyrroles, indoles, imidazoles, benzoxazoles, and furans. Preliminary studies suggest that this reaction may proceed via the catalytic formation of highly electrophilic intermediates. Overall, this provides with an atom-economical and general synthetic route to generate aryl-(hetero)aryl ketones using stable reagents (aryl iodides and CO) and without the typical need to exploit pre-metalated heterocycles in carbonylative coupling chemistry.

ANXIOLYTIC AROYL PIPERIDINYL AND PIPERAZINYLACYL PYRROLES

-

, (2008/06/13)

Aroyl(piperidinyl and piperazinyl)acyl pyrroles of the following formula have anxiolytic activity: STR1 wherein, Y is selected from the group consisting of N, CH or COH;A. sup.1 is selected from the group consisting of STR2 n is an integer from 1 to

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