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1188392-24-6

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  • 1188392-24-6 Structure

  • Basic information

    1. Product Name: N-benzyl-N-(3-phenylprop-2-yn-1-yl)prop-2-en-1-amine
    2. Synonyms: N-benzyl-N-(3-phenylprop-2-yn-1-yl)prop-2-en-1-amine
    3. CAS NO:1188392-24-6
    4. Molecular Formula:
    5. Molecular Weight: 261.367
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1188392-24-6.mol
    9. Article Data: 4

  • 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: N-benzyl-N-(3-phenylprop-2-yn-1-yl)prop-2-en-1-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl-N-(3-phenylprop-2-yn-1-yl)prop-2-en-1-amine(1188392-24-6)
    11. EPA Substance Registry System: N-benzyl-N-(3-phenylprop-2-yn-1-yl)prop-2-en-1-amine(1188392-24-6)

  • 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: 1188392-24-6(Hazardous Substances Data)

1188392-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1188392-24-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,8,3,9 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1188392-24:
(9*1)+(8*1)+(7*8)+(6*8)+(5*3)+(4*9)+(3*2)+(2*2)+(1*4)=186
186 % 10 = 6
So 1188392-24-6 is a valid CAS Registry Number.

1188392-24-6Relevant articles and documents

Palladium-Catalyzed Carboxy-Alkynylation of Propargylic Amines Using Carbonate Salts as Carbon Dioxide Source

Greenwood, Phillip D. G.,Waser, Jerome

supporting information, p. 5183 - 5186 (2019/06/10)

A palladium-catalyzed multicomponent reaction of propargylic amines, alkynyl bromides and cesium hydrogen carbonate to access oxazolidinones is reported. In contrast to previous reports, only a slight excess of cesium hydrogen carbonate is used as a surrogate of carbon dioxide. The reaction gives access to oxazolidinones bearing alkyl- and aryl polysubstituted enynes in good yield and very high E stereoselectivity.

Reaction of bicyclic zirconacyclopentenes with aldehydes and a potential pathway to condensed 5-7-6(Ar) ring systems

Topolovan, Nikola,Panov, Illia,Kotora, Martin

supporting information, p. 2868 - 2878 (2015/08/04)

Bicyclic zirconacyclopentenes prepared by the reactions of 1,6- and 1,7-enynes with [Cp2ZrBu2] (Negishi reagent) reacted with a plethora of aldehydes (aryl, heteroaryl, alkyl, α,β-unsaturated) by chemo- and stereoselective insertion

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