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132960-16-8

1-(5-methylthiophen-2-yl)-3-phenylprop-2-yn-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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  • 132960-16-8 Structure

  • Basic information

    1. Product Name: 1-(5-methylthiophen-2-yl)-3-phenylprop-2-yn-1-one
    2. Synonyms: 1-(5-methylthiophen-2-yl)-3-phenylprop-2-yn-1-one
    3. CAS NO:132960-16-8
    4. Molecular Formula:
    5. Molecular Weight: 226.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132960-16-8.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-(5-methylthiophen-2-yl)-3-phenylprop-2-yn-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(5-methylthiophen-2-yl)-3-phenylprop-2-yn-1-one(132960-16-8)
    11. EPA Substance Registry System: 1-(5-methylthiophen-2-yl)-3-phenylprop-2-yn-1-one(132960-16-8)

  • 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: 132960-16-8(Hazardous Substances Data)

132960-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132960-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,6 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132960-16:
(8*1)+(7*3)+(6*2)+(5*9)+(4*6)+(3*0)+(2*1)+(1*6)=118
118 % 10 = 8
So 132960-16-8 is a valid CAS Registry Number.

132960-16-8Downstream Products

132960-16-8Relevant articles and documents

Stitching Ynones with Nitromethanes: Domino Synthesis of Functionally Enriched Benzofurans and Benzothiophenes

Mehta, Goverdhan,Nerella, Sharanya,Pabbaraja, Srihari,Singh, Shweta

, p. 12093 - 12106 (2021/09/13)

A convenient one-pot benzannulation of regioisomeric 2- or 3-substituted furan and thiophene ynones with a range of nitromethanes has been discovered to directly access densely and diversely functionalized benzofurans and benzothiophenes. In this protocol, the nitro group in nitromethanes functions as recursive carbanion activator to setup tandem Michael addition-6π-electrocyclization, and its eventual sacrificial elimination facilitates aromatization and overall benzannulation. This benzannulation was also explored with furan/thiophene based o-halo ynones wherein a Michael addition-SNAr process operates and nitromethanes leave their imprint to deliver nitro substituted benzo-furans and -thiophenes.

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