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1434751-77-5

2-benzoyl-4-(4-bromophenyl)-1-phenylbut-2-ene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1434751-77-5 Structure

  • Basic information

    1. Product Name: 2-benzoyl-4-(4-bromophenyl)-1-phenylbut-2-ene-1,4-dione
    2. Synonyms: 2-benzoyl-4-(4-bromophenyl)-1-phenylbut-2-ene-1,4-dione
    3. CAS NO:1434751-77-5
    4. Molecular Formula:
    5. Molecular Weight: 419.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1434751-77-5.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: 2-benzoyl-4-(4-bromophenyl)-1-phenylbut-2-ene-1,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzoyl-4-(4-bromophenyl)-1-phenylbut-2-ene-1,4-dione(1434751-77-5)
    11. EPA Substance Registry System: 2-benzoyl-4-(4-bromophenyl)-1-phenylbut-2-ene-1,4-dione(1434751-77-5)

  • 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: 1434751-77-5(Hazardous Substances Data)

1434751-77-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1434751-77-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,4,7,5 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1434751-77:
(9*1)+(8*4)+(7*3)+(6*4)+(5*7)+(4*5)+(3*1)+(2*7)+(1*7)=165
165 % 10 = 5
So 1434751-77-5 is a valid CAS Registry Number.

1434751-77-5Relevant articles and documents

An Expedient, Direct, Three-Component Approach for the Synthesis of 4-Thioarylpyrroles

Anandan, Sambandam,Neelamegam, Chinnaraj,Rajeshkumar, Venkatachalam

, p. 4023 - 4033 (2019)

A three-component strategy for the synthesis of 4-thioarylpyrroles from 1,4-enediones, thiols, and ammonium formate in one-pot has been developed. The reaction proceeds through the sequential thiol-Michael/Paal-Knorr reaction of 1,4-enediones with the for

Target-oriented synthesis: Miscellaneous synthetic routes to access 1,4-enediones through the coupling of 1,3-dicarbonyl compounds with multiform substrates

Zhu, Yan-Ping,Cai, Qun,Gao, Qing-He,Jia, Feng-Cheng,Liu, Mei-Cai,Gao, Meng,Wu, An-Xin

, p. 6392 - 6398 (2013/07/25)

Target-oriented synthetic protocol was presented for the synthesis of 1,4-enediones. The approach can efficiently construct 1,4-enediones through different reaction pathways from multiform substrates α-halo aromatic ketones, 2-hydroxy-aromatic ketones and methyl carbinols. In this reaction, CuI was found to be the most efficient catalyst. Multiform substrates were also found to perform well to afford the products in a one-pot fashion.

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