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1427729-26-7

(4-(benzyloxy)dec-2-yn-1-yl)pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1427729-26-7 Structure

  • Basic information

    1. Product Name: (4-(benzyloxy)dec-2-yn-1-yl)pyrrolidine
    2. Synonyms: (4-(benzyloxy)dec-2-yn-1-yl)pyrrolidine
    3. CAS NO:1427729-26-7
    4. Molecular Formula:
    5. Molecular Weight: 313.483
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1427729-26-7.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: (4-(benzyloxy)dec-2-yn-1-yl)pyrrolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-(benzyloxy)dec-2-yn-1-yl)pyrrolidine(1427729-26-7)
    11. EPA Substance Registry System: (4-(benzyloxy)dec-2-yn-1-yl)pyrrolidine(1427729-26-7)

  • 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: 1427729-26-7(Hazardous Substances Data)

1427729-26-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427729-26-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,7,2 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1427729-26:
(9*1)+(8*4)+(7*2)+(6*7)+(5*7)+(4*2)+(3*9)+(2*2)+(1*6)=177
177 % 10 = 7
So 1427729-26-7 is a valid CAS Registry Number.

1427729-26-7Downstream Products

1427729-26-7Relevant articles and documents

Pd(0)-catalyzed alkene oxy- and aminoalkynylation with aliphatic bromoacetylenes

Nicolai, Stefano,Sedigh-Zadeh, Raha,Waser, Jeroime

, p. 3783 - 3801 (2013/06/26)

Tetrahydrofurans and pyrrolidines are among the most important heterocycles found in bioactive compounds. Cyclization-functionalization domino reactions of alcohols or amines onto olefins constitute one of the most efficient methods to access them. In this context, oxy- and aminoalkynylation are especially important reactions, because of the numerous transformations possible with the triple bond of acetylenes, yet these methods have been limited to the use of silyl protected acetylenes. Herein, we report the first palladium-catalyzed oxy- and aminoalkynylation using aliphatic bromoalkynes, which proceeded with high diastereoselectivity and functional group tolerance. A one-pot hydrogenation of the triple bond gave then access to alkyl-substituted tetrahydrofurans and pyrroldines. Finally, a detailed study of the side products formed during the reaction gave a first insight into the reaction mechanism.

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