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1-hexadecyl-4-methylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 154177-08-9 Structure
  • Basic information

    1. Product Name: 1-hexadecyl-4-methylbenzene
    2. Synonyms: 1-Hexadecyl-4-methylbenzene; benzene, 1-hexadecyl-4-methyl-
    3. CAS NO:154177-08-9
    4. Molecular Formula: C23H40
    5. Molecular Weight: 316.5637
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154177-08-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 409.4°C at 760 mmHg
    3. Flash Point: 201.7°C
    4. Appearance: N/A
    5. Density: 0.856g/cm3
    6. Vapor Pressure: 1.54E-06mmHg at 25°C
    7. Refractive Index: 1.482
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-hexadecyl-4-methylbenzene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-hexadecyl-4-methylbenzene(154177-08-9)
    12. EPA Substance Registry System: 1-hexadecyl-4-methylbenzene(154177-08-9)
  • 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: 154177-08-9(Hazardous Substances Data)

154177-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154177-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,1,7 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 154177-08:
(8*1)+(7*5)+(6*4)+(5*1)+(4*7)+(3*7)+(2*0)+(1*8)=129
129 % 10 = 9
So 154177-08-9 is a valid CAS Registry Number.

154177-08-9Relevant articles and documents

Iron catalyzed cross coupling reactions of aromatic compounds

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Page/Page column 6, (2010/02/03)

A process for the production of compounds Ar—R1 by means of a cross-coupling reaction of an organometallic reagent R1—M with an aromatic or heteroaromatic substrate Ar—X catalyzed by one or several iron salts or iron complexes as catalysts or pre-catalysts, present homogeneously or heterogeneously in the reaction mixture. This new invention exhibits substantial advantages over established cross coupling methodology using palladium- or nickel complexes as the catalysts. Most notable aspects are the fact that (i) expensive and/or toxic nobel metal catalysts are replaced by cheap, stable, commercially available and toxicologically benign iron salts or iron complexes as the catalysts or pre-catalysts, (ii) commercially attractive aryl chlorides as well as various aryl sulfonates can be used as starting materials, (iii) the reaction can be performed under “ligand-free” conditons, and (iv) the reaction times are usually very short.

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