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CAS

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314777-60-1

Benzene, 1,4-dihexadecyl-2,5-diiodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 314777-60-1 Structure

  • Basic information

    1. Product Name: Benzene, 1,4-dihexadecyl-2,5-diiodo-
    2. Synonyms:
    3. CAS NO:314777-60-1
    4. Molecular Formula: C38H68I2
    5. Molecular Weight: 778.767
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 314777-60-1.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: Benzene, 1,4-dihexadecyl-2,5-diiodo-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, 1,4-dihexadecyl-2,5-diiodo-(314777-60-1)
    11. EPA Substance Registry System: Benzene, 1,4-dihexadecyl-2,5-diiodo-(314777-60-1)

  • 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: 314777-60-1(Hazardous Substances Data)

314777-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 314777-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,4,7,7 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 314777-60:
(8*3)+(7*1)+(6*4)+(5*7)+(4*7)+(3*7)+(2*6)+(1*0)=151
151 % 10 = 1
So 314777-60-1 is a valid CAS Registry Number.

314777-60-1Downstream Products

314777-60-1Relevant articles and documents

Efficient synthesis of 1,4-dialkoxy and 1,4-dialkyl substituted 2,5-divinylbenzenes via the Stille reaction

Daoud, Walid A.,Turner, Michael L.

, p. 367 - 369 (2005)

An efficient palladium catalyzed cross coupling of tributyl(vinyl)stannane with dialkoxy and dialkyl substituted 1,4-dihalobenzenes is described. This single-step coupling provides an efficient synthesis of functionalized 2,5-divinylbenzenes, which are us

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