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1-(5-(2-methoxypropan-2-yl)cyclopent-1-enyl)-2-(2-methylprop-1-enyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1346697-15-1 Structure
  • Basic information

    1. Product Name: 1-(5-(2-methoxypropan-2-yl)cyclopent-1-enyl)-2-(2-methylprop-1-enyl)benzene
    2. Synonyms:
    3. CAS NO:1346697-15-1
    4. Molecular Formula:
    5. Molecular Weight: 270.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1346697-15-1.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: 1-(5-(2-methoxypropan-2-yl)cyclopent-1-enyl)-2-(2-methylprop-1-enyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(5-(2-methoxypropan-2-yl)cyclopent-1-enyl)-2-(2-methylprop-1-enyl)benzene(1346697-15-1)
    11. EPA Substance Registry System: 1-(5-(2-methoxypropan-2-yl)cyclopent-1-enyl)-2-(2-methylprop-1-enyl)benzene(1346697-15-1)
  • 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: 1346697-15-1(Hazardous Substances Data)

1346697-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1346697-15-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,6,9 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1346697-15:
(9*1)+(8*3)+(7*4)+(6*6)+(5*6)+(4*9)+(3*7)+(2*1)+(1*5)=191
191 % 10 = 1
So 1346697-15-1 is a valid CAS Registry Number.

1346697-15-1Downstream Products

1346697-15-1Relevant articles and documents

Nature of the intermediates in gold(I)-catalyzed cyclizations of 1,5-enynes

Lopez-Carrillo, Veronica,Huguet, Nuria,Mosquera, Ungeles,Echavarren, Antonio M.

, p. 10972 - 10978 (2011)

The carbene or carbocationic nature of the intermediates in the gold-catalyzed cycloisomerization of 1,5-enynes can be revealed, depending on the ligands on the gold catalysts. Gold complexes with highly electron-donating ligands promote reactions that proceed via intermediates with carbene-like character, leading to products with a bicyclo[3.1.0]hexene skeleton. The intermediate cyclopropyl endo-gold carbenes formed in this cyclization have been trapped, for the first time, to give biscyclopropane derivatives in a reaction that proceeds in a concerted fashion, according to DFT calculations.

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