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1416051-33-6

7-phenylhepta-5,6-dien-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1416051-33-6 Structure

  • Basic information

    1. Product Name: 7-phenylhepta-5,6-dien-1-ol
    2. Synonyms: 7-phenylhepta-5,6-dien-1-ol
    3. CAS NO:1416051-33-6
    4. Molecular Formula:
    5. Molecular Weight: 188.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1416051-33-6.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: 7-phenylhepta-5,6-dien-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-phenylhepta-5,6-dien-1-ol(1416051-33-6)
    11. EPA Substance Registry System: 7-phenylhepta-5,6-dien-1-ol(1416051-33-6)

  • 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: 1416051-33-6(Hazardous Substances Data)

1416051-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1416051-33-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,0,5 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1416051-33:
(9*1)+(8*4)+(7*1)+(6*6)+(5*0)+(4*5)+(3*1)+(2*3)+(1*3)=116
116 % 10 = 6
So 1416051-33-6 is a valid CAS Registry Number.

1416051-33-6Relevant articles and documents

Stereoselective synthesis of chiral polycyclic indolic architectures through Pd0-catalyzed tandem deprotection/cyclization of tetrahydro-β-carbolines on allenes

Gobé, Valérian,Guinchard, Xavier

, p. 8511 - 8520 (2015)

Enantioenriched N-allyl tetrahydro-β-carbolines were prepared by chiral phosphoric acid-catalyzed Pictet-Spengler reactions. The compounds undergo Pd0-catalyzed cyclizations through a tandem deprotection/cyclization process. The regioselectivit

Domino formation of enamines - Intramolecular cyclizations to 1-aminotetralins from γ-arylallene aldehydes and amines

Gob, Valrian,Retailleau, Pascal,Guinchard, Xavier

, p. 5438 - 5441 (2014)

1,5-/1,6-Allenals conjugated to an aromatic ring undergo a cyclization, in the presence of an amine, that leads to tricyclic compounds including the 1-aminotetralin scaffold. This domino process combines the in situ formation of the enamine and the cyclization affording the tricyclic 1-aminotetralins in very high diastereoselectivities. (Chemical Equation Presented).

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