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66217-97-8

Pyrrolidine, 1-(2-phenyl-1-propenyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 66217-97-8 Structure

  • Basic information

    1. Product Name: Pyrrolidine, 1-(2-phenyl-1-propenyl)-, (Z)-
    2. Synonyms:
    3. CAS NO:66217-97-8
    4. Molecular Formula: C13H17N
    5. Molecular Weight: 187.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 66217-97-8.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: Pyrrolidine, 1-(2-phenyl-1-propenyl)-, (Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrrolidine, 1-(2-phenyl-1-propenyl)-, (Z)-(66217-97-8)
    11. EPA Substance Registry System: Pyrrolidine, 1-(2-phenyl-1-propenyl)-, (Z)-(66217-97-8)

  • 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: 66217-97-8(Hazardous Substances Data)

66217-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66217-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,1 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66217-97:
(7*6)+(6*6)+(5*2)+(4*1)+(3*7)+(2*9)+(1*7)=138
138 % 10 = 8
So 66217-97-8 is a valid CAS Registry Number.

66217-97-8Downstream Products

66217-97-8Relevant articles and documents

Enamines as Surrogates of Alkyl Carbanions for the Direct Conversion of Secondary Amides to α-Branched Ketones

Liu, Yong-Peng,Wang, Shu-Ren,Chen, Ting-Ting,Yu, Cun-Cun,Wang, Ai-E,Huang, Pei-Qiang

, p. 971 - 975 (2019)

A direct transformation of secondary amides into α-branched ketones with enamines as soft alkylation reagents was developed. In this reaction, enamines serve as surrogates of alkyl carbanions, rather than the conventional enolates equivalents in the Stork's reactions, which allowed for the easy introduction of alkyl groups with electrophilic functional groups. In the presence of 4 ? molecular sieves, the method can be extended to the one-pot coupling of secondary amides with aldehydes to yield ketones. (Figure presented.).

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