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CAS

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1442416-25-2

5-cyclohexyl-1,2,3-trimethoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1442416-25-2 Structure

  • Basic information

    1. Product Name: 5-cyclohexyl-1,2,3-trimethoxybenzene
    2. Synonyms: 5-cyclohexyl-1,2,3-trimethoxybenzene
    3. CAS NO:1442416-25-2
    4. Molecular Formula:
    5. Molecular Weight: 250.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1442416-25-2.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: 5-cyclohexyl-1,2,3-trimethoxybenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-cyclohexyl-1,2,3-trimethoxybenzene(1442416-25-2)
    11. EPA Substance Registry System: 5-cyclohexyl-1,2,3-trimethoxybenzene(1442416-25-2)

  • 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: 1442416-25-2(Hazardous Substances Data)

1442416-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1442416-25-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,2,4,1 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1442416-25:
(9*1)+(8*4)+(7*4)+(6*2)+(5*4)+(4*1)+(3*6)+(2*2)+(1*5)=132
132 % 10 = 2
So 1442416-25-2 is a valid CAS Registry Number.

1442416-25-2Downstream Products

1442416-25-2Relevant articles and documents

Cobalt-Catalyzed C(sp2)-C(sp3) Cross-Coupling Reactions of Diarylmanganese Reagents with Secondary Alkyl Iodides

Hofmayer, Maximilian S.,Hammann, Jeffrey M.,Haas, Diana,Knochel, Paul

, p. 6456 - 6459 (2016/12/23)

A cobalt-catalyzed cross-coupling of diarylmanganese reagents with secondary alkyl iodides using the THF-soluble salt CoCl2·2LiCl, which leads to the cross-coupling products in up to 92% yield, is reported. High diastereoselectivities can be re

Sterically controlled alkylation of arenes through iridium-catalyzed C-H borylation

Robbins, Daniel W.,Hartwig, John F.

, p. 933 - 937 (2013/02/25)

Complementary chemistry: A one-pot method for the site-selective alkylation of arenes controlled by steric effects is reported. The process occurs through Ir-catalyzed C-H borylation, followed by Pd- or Ni-catalyzed coupling with alkyl electrophiles. This selectivity complements that of the typical Friedel-Crafts alkylation; meta-selective alkylation of a broad range of arenes with various electronic properties and functional groups occurs in good yield with high site selectivity. Copyright

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