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144650-27-1

Benzene, [(1-ethyl-5-phenyl-1,5-hexadienyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144650-27-1 Structure

  • Basic information

    1. Product Name: Benzene, [(1-ethyl-5-phenyl-1,5-hexadienyl)thio]-
    2. Synonyms:
    3. CAS NO:144650-27-1
    4. Molecular Formula: C20H22S
    5. Molecular Weight: 294.461
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144650-27-1.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-ethyl-5-phenyl-1,5-hexadienyl)thio]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [(1-ethyl-5-phenyl-1,5-hexadienyl)thio]-(144650-27-1)
    11. EPA Substance Registry System: Benzene, [(1-ethyl-5-phenyl-1,5-hexadienyl)thio]-(144650-27-1)

  • 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: 144650-27-1(Hazardous Substances Data)

144650-27-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144650-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,6,5 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 144650-27:
(8*1)+(7*4)+(6*4)+(5*6)+(4*5)+(3*0)+(2*2)+(1*7)=121
121 % 10 = 1
So 144650-27-1 is a valid CAS Registry Number.

144650-27-1Downstream Products

144650-27-1Relevant articles and documents

The tin(IV) chloride-promoted cross-coupling reaction of allylstannanes with allylsilanes

Takeda, Takeshi,Takagi, Yu,Takano, Hiroki,Fujiwara, Tooru

, p. 5381 - 5384 (2007/10/02)

The cross-coupling reaction of allylstannanes with allylsilanes selectively proceeded in the presence of tin(IV) chloride to give 1,5-dienes. It was found that the substitution of a phenylthio group at γ-position remarkably increased the reactivity of all

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