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1446356-86-0

(2-bromo-3,4,5-trimethoxyphenyl)(cyclohexyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446356-86-0 Structure

  • Basic information

    1. Product Name: (2-bromo-3,4,5-trimethoxyphenyl)(cyclohexyl)methanone
    2. Synonyms: (2-bromo-3,4,5-trimethoxyphenyl)(cyclohexyl)methanone
    3. CAS NO:1446356-86-0
    4. Molecular Formula:
    5. Molecular Weight: 357.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446356-86-0.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-bromo-3,4,5-trimethoxyphenyl)(cyclohexyl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-bromo-3,4,5-trimethoxyphenyl)(cyclohexyl)methanone(1446356-86-0)
    11. EPA Substance Registry System: (2-bromo-3,4,5-trimethoxyphenyl)(cyclohexyl)methanone(1446356-86-0)

  • 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: 1446356-86-0(Hazardous Substances Data)

1446356-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446356-86-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,3,5 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1446356-86:
(9*1)+(8*4)+(7*4)+(6*6)+(5*3)+(4*5)+(3*6)+(2*8)+(1*6)=180
180 % 10 = 0
So 1446356-86-0 is a valid CAS Registry Number.

1446356-86-0Downstream Products

1446356-86-0Relevant articles and documents

Formation of bi-aryls via a domino palladium catalysis

Krishna,Gopi Krishna Reddy,Satyanarayana

, p. 861 - 864 (2015/03/05)

Synthesis of bi-aryls via a domino Pd-catalyzed reaction of 1-(2-bromophenyl)-2-methylpropan-1-ones/(2-bromophenyl)(cyclohexyl)methanones is presented. The mechanism of the reaction is believed to proceed through a five membered palladacycle that combines with a second molecule of halo-arene to yield the bi-aryls. This method is quite successful to deliver highly sterically crowded bi-aryls with dense functionalities on the aromatic rings.

Formation of bi-aryls via a domino palladium catalysis

Krishna,Reddy, A. Gopi Krishna,Satyanarayana

, p. 861 - 864 (2014/02/14)

Synthesis of bi-aryls via a domino Pd-catalyzed reaction of 1-(2-bromophenyl)-2-methylpropan-1-ones/(2-bromophenyl)(cyclohexyl)methanones is presented. The mechanism of the reaction is believed to proceed through a five membered palladacycle that combines with a second molecule of halo-arene to yield the bi-aryls. This method is quite successful to deliver highly sterically crowded bi-aryls with dense functionalities on the aromatic rings.

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