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CAS

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1608108-44-6

(E)-1-(1H-pyrrol-1-yl)-3-(m-tolyl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1608108-44-6 Structure

  • Basic information

    1. Product Name: (E)-1-(1H-pyrrol-1-yl)-3-(m-tolyl)prop-2-en-1-one
    2. Synonyms: (E)-1-(1H-pyrrol-1-yl)-3-(m-tolyl)prop-2-en-1-one
    3. CAS NO:1608108-44-6
    4. Molecular Formula:
    5. Molecular Weight: 211.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1608108-44-6.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: (E)-1-(1H-pyrrol-1-yl)-3-(m-tolyl)prop-2-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-(1H-pyrrol-1-yl)-3-(m-tolyl)prop-2-en-1-one(1608108-44-6)
    11. EPA Substance Registry System: (E)-1-(1H-pyrrol-1-yl)-3-(m-tolyl)prop-2-en-1-one(1608108-44-6)

  • 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: 1608108-44-6(Hazardous Substances Data)

1608108-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1608108-44-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,8,1,0 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1608108-44:
(9*1)+(8*6)+(7*0)+(6*8)+(5*1)+(4*0)+(3*8)+(2*4)+(1*4)=146
146 % 10 = 6
So 1608108-44-6 is a valid CAS Registry Number.

1608108-44-6Relevant articles and documents

An approach for rapid increase in molecular complexity: Atom economic routes to fused polycyclic ring systems

Trost, Barry M.,Ehmke, Veronika

, p. 2708 - 2711 (2014)

A protocol for the asymmetric trimethylenemethane (TMM) [3 + 2] cycloaddition reaction of alkynyl-substituted TMM donors and unsaturated N-acyl pyrroles employing a chiral bisdiamidophosphite ligand has been developed. This process generates alkynyl-substituted cyclopentanes in high yields and diastereo- and enantioselectivities. These chiral precursors are employed for the atom economic assembly of fused polycyclic hydrocarbons with hydroindene, hydroazulene, and hydrocyclopentanaphthalene scaffolds by consecutive cycloaddition reactions.

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