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CAS

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1446428-46-1

8-(2-phenylethynyl)chromone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446428-46-1 Structure

  • Basic information

    1. Product Name: 8-(2-phenylethynyl)chromone
    2. Synonyms:
    3. CAS NO:1446428-46-1
    4. Molecular Formula:
    5. Molecular Weight: 246.265
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446428-46-1.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: 8-(2-phenylethynyl)chromone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-(2-phenylethynyl)chromone(1446428-46-1)
    11. EPA Substance Registry System: 8-(2-phenylethynyl)chromone(1446428-46-1)

  • 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: 1446428-46-1(Hazardous Substances Data)

1446428-46-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446428-46-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,4,2 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1446428-46:
(9*1)+(8*4)+(7*4)+(6*6)+(5*4)+(4*2)+(3*8)+(2*4)+(1*6)=171
171 % 10 = 1
So 1446428-46-1 is a valid CAS Registry Number.

1446428-46-1Downstream Products

1446428-46-1Relevant articles and documents

C-alkynylation of chromones by sonogashira reaction

Patonay, Tamas,Pazurik, Istvan,Abraham, Anita

, p. 646 - 654 (2013/07/26)

Sonogashira reaction of bromochromones and-flavones with a bromine atom on their benzene or heterocyclic ring with various terminal alkynes gave the desired products with nearly the same efficiency as the previously used iodine derivatives. The coupling reactions were performed in the presence of [tetrakis(triphenylphosphine)palladium(0)], copper(i) co-catalyst, and triethylamine, resulting in the formation of numerous hitherto unknown alkynylated oxygen heterocycles, and provide further proof for the applicability of this reaction for these O-heterocycles. Chromones with ethynyl functionality were prepared by removal of the trimethylsilyl protecting group and used as terminal alkynes in a second cross-coupling reaction.

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