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3-(3,5-di((Z)-dec-1-enyl)-4,6-dimethylpyridin-2-yl)propan-1-ol hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1333320-21-0 Structure
  • Basic information

    1. Product Name: 3-(3,5-di((Z)-dec-1-enyl)-4,6-dimethylpyridin-2-yl)propan-1-ol hydrochloride
    2. Synonyms:
    3. CAS NO:1333320-21-0
    4. Molecular Formula:
    5. Molecular Weight: 478.202
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1333320-21-0.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: 3-(3,5-di((Z)-dec-1-enyl)-4,6-dimethylpyridin-2-yl)propan-1-ol hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(3,5-di((Z)-dec-1-enyl)-4,6-dimethylpyridin-2-yl)propan-1-ol hydrochloride(1333320-21-0)
    11. EPA Substance Registry System: 3-(3,5-di((Z)-dec-1-enyl)-4,6-dimethylpyridin-2-yl)propan-1-ol hydrochloride(1333320-21-0)
  • 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: 1333320-21-0(Hazardous Substances Data)

1333320-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333320-21-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,3,2 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1333320-21:
(9*1)+(8*3)+(7*3)+(6*3)+(5*3)+(4*2)+(3*0)+(2*2)+(1*1)=100
100 % 10 = 0
So 1333320-21-0 is a valid CAS Registry Number.

1333320-21-0Downstream Products

1333320-21-0Relevant articles and documents

Regio- and stereoselective syntheses of the natural product CCR5 antagonist anibamine and its three olefin isomers

Zhang, Feng,Zaidi, Saheem,Haney, Kendra M.,Kellogg, Glen E.,Zhang, Yan

, p. 7945 - 7952 (2011/11/30)

The syntheses of the natural product anibamine and its three olefin isomers have been achieved concisely and efficiently via highly regio- and stereoselective reactions. The crucial steps included a regioselective palladium-catalyzed alkynylation by Sonogashira coupling and a stereoselective Suzuki coupling. Further conformation analyses and in vitro calcium mobilization studies were carried out to characterize the compounds' biological properties.

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