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1085323-21-2

2,4,6-tris(4-tert-butylphenoxy)benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1085323-21-2 Structure

  • Basic information

    1. Product Name: 2,4,6-tris(4-tert-butylphenoxy)benzonitrile
    2. Synonyms: 2,4,6-tris(4-tert-butylphenoxy)benzonitrile
    3. CAS NO:1085323-21-2
    4. Molecular Formula:
    5. Molecular Weight: 547.737
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1085323-21-2.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: 2,4,6-tris(4-tert-butylphenoxy)benzonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4,6-tris(4-tert-butylphenoxy)benzonitrile(1085323-21-2)
    11. EPA Substance Registry System: 2,4,6-tris(4-tert-butylphenoxy)benzonitrile(1085323-21-2)

  • 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: 1085323-21-2(Hazardous Substances Data)

1085323-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1085323-21-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,5,3,2 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1085323-21:
(9*1)+(8*0)+(7*8)+(6*5)+(5*3)+(4*2)+(3*3)+(2*2)+(1*1)=132
132 % 10 = 2
So 1085323-21-2 is a valid CAS Registry Number.

1085323-21-2Downstream Products

1085323-21-2Relevant articles and documents

Diaryl ether synthesis in supercritical carbon dioxide in batch and continuous flow modes

Lee, Jin-Kyun,Fuchter, Matthew J.,Williamson, Rachel M.,Leeke, Gary A.,Bush, Edward J.,McConvey, Ian F.,Saubern, Simon,Ryan, John H.,Holmes, Andrew B.

, p. 4780 - 4782 (2008)

A high yielding, batch mode synthesis of diaryl ethers and sulfides by an SNAr fluoride-mediated process in scCO2 has been developed; the use of a polymer-supported imidazolium fluoride reagent in batch mode led to the development of

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