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1203669-25-3

1-(2,5-dibromophenyl)-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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  • 1203669-25-3 Structure

  • Basic information

    1. Product Name: 1-(2,5-dibromophenyl)-3-phenylprop-2-yn-1-one
    2. Synonyms: 1-(2,5-dibromophenyl)-3-phenylprop-2-yn-1-one
    3. CAS NO:1203669-25-3
    4. Molecular Formula:
    5. Molecular Weight: 364.036
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1203669-25-3.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-(2,5-dibromophenyl)-3-phenylprop-2-yn-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2,5-dibromophenyl)-3-phenylprop-2-yn-1-one(1203669-25-3)
    11. EPA Substance Registry System: 1-(2,5-dibromophenyl)-3-phenylprop-2-yn-1-one(1203669-25-3)

  • 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: 1203669-25-3(Hazardous Substances Data)

1203669-25-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1203669-25-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,3,6,6 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1203669-25:
(9*1)+(8*2)+(7*0)+(6*3)+(5*6)+(4*6)+(3*9)+(2*2)+(1*5)=133
133 % 10 = 3
So 1203669-25-3 is a valid CAS Registry Number.

1203669-25-3Upstream product

1203669-25-3Downstream Products

1203669-25-3Relevant articles and documents

Palladium-catalyzed tandem amination reaction for the synthesis of 4-quinolones

Zhao, Tlankun,Xu, Bin

, p. 212 - 215 (2010)

(Figure presented) An efficient palladium-catalyzed tandem amlnatlon approach was developed In one step to afford functlonallzed 4-qulnolones In good to excellent ylelds from easlly accessible o-haloaryl acetylenlc ketones and primary amines.

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