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1609102-33-1

2-cyclohexenyl-4-methoxy-1-nitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1609102-33-1 Structure

  • Basic information

    1. Product Name: 2-cyclohexenyl-4-methoxy-1-nitrobenzene
    2. Synonyms: 2-cyclohexenyl-4-methoxy-1-nitrobenzene
    3. CAS NO:1609102-33-1
    4. Molecular Formula:
    5. Molecular Weight: 233.267
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1609102-33-1.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: 2-cyclohexenyl-4-methoxy-1-nitrobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-cyclohexenyl-4-methoxy-1-nitrobenzene(1609102-33-1)
    11. EPA Substance Registry System: 2-cyclohexenyl-4-methoxy-1-nitrobenzene(1609102-33-1)

  • 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: 1609102-33-1(Hazardous Substances Data)

1609102-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609102-33-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,1,0 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1609102-33:
(9*1)+(8*6)+(7*0)+(6*9)+(5*1)+(4*0)+(3*2)+(2*3)+(1*3)=131
131 % 10 = 1
So 1609102-33-1 is a valid CAS Registry Number.

1609102-33-1Downstream Products

1609102-33-1Relevant articles and documents

Arylalkene synthesis via decarboxylative cross-coupling of alkenyl halides

Tang, Jie,Goossen, Lukas J.

, p. 2664 - 2667 (2014)

A bimetallic catalyst system generated from readily available palladium(II) and copper(I) salts, 1,10-phenanthroline and tri-1-naphthylphosphine was found to efficiently mediate the decarboxylative cross-coupling of alkenyl bromides and chlorides with aromatic carboxylates. It allows the regiospecific synthesis of a broad range of aryl- and heteroarylalkenes in high yields.

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