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1034286-99-1

ethyl 2-phenyl-3,6-di[4-(2',3'-dimethylbutan-2',3'-dioxoboryl)phenyl]benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1034286-99-1 Structure

  • Basic information

    1. Product Name: ethyl 2-phenyl-3,6-di[4-(2',3'-dimethylbutan-2',3'-dioxoboryl)phenyl]benzoate
    2. Synonyms: ethyl 2-phenyl-3,6-di[4-(2',3'-dimethylbutan-2',3'-dioxoboryl)phenyl]benzoate
    3. CAS NO:1034286-99-1
    4. Molecular Formula:
    5. Molecular Weight: 630.397
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1034286-99-1.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: ethyl 2-phenyl-3,6-di[4-(2',3'-dimethylbutan-2',3'-dioxoboryl)phenyl]benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-phenyl-3,6-di[4-(2',3'-dimethylbutan-2',3'-dioxoboryl)phenyl]benzoate(1034286-99-1)
    11. EPA Substance Registry System: ethyl 2-phenyl-3,6-di[4-(2',3'-dimethylbutan-2',3'-dioxoboryl)phenyl]benzoate(1034286-99-1)

  • 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: 1034286-99-1(Hazardous Substances Data)

1034286-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034286-99-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,2,8 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1034286-99:
(9*1)+(8*0)+(7*3)+(6*4)+(5*2)+(4*8)+(3*6)+(2*9)+(1*9)=141
141 % 10 = 1
So 1034286-99-1 is a valid CAS Registry Number.

1034286-99-1Downstream Products

1034286-99-1Relevant articles and documents

Manganese-catalyzed benzene synthesis by [2+2+2] coupling of 1,3-dicarbonyl compound and terminal acetylene

Tsuji, Hayato,Yamagata, Ken-Ichi,Fujimoto, Taisuke,Nakamura, Eiichi

, p. 7792 - 7793 (2009/02/02)

Treatment of a mixture of a 1,3-dicarbonyl compound such as a β-ketoester or 1,3-ketone and a terminal acetylene with a catalytic amount of MnBr(CO)5 in heated toluene produces a benzene derivative by a [2+2+2] coupling reaction incorporating the enol part of the dicarbonyl compound and two moles of the acetylene. When the reaction was carried out using phenylacetylene derivatives, the reaction was completely regioselective, producing p-terphenyl compounds in good to excellent yield. Aliphatic terminal acetylenes also reacted readily but gave a mixture of regioisomers. The reaction features high atom economy, neutral conditions, and functional group tolerance, and will be useful for materials-oriented studies. Copyright

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