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CAS

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22148-83-0

N-methyl-1-methyl-4-phenylbutylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22148-83-0 Structure

  • Basic information

    1. Product Name: N-methyl-1-methyl-4-phenylbutylamine
    2. Synonyms:
    3. CAS NO:22148-83-0
    4. Molecular Formula:
    5. Molecular Weight: 177.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22148-83-0.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: N-methyl-1-methyl-4-phenylbutylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-methyl-1-methyl-4-phenylbutylamine(22148-83-0)
    11. EPA Substance Registry System: N-methyl-1-methyl-4-phenylbutylamine(22148-83-0)

  • 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: 22148-83-0(Hazardous Substances Data)

22148-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22148-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,4 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22148-83:
(7*2)+(6*2)+(5*1)+(4*4)+(3*8)+(2*8)+(1*3)=90
90 % 10 = 0
So 22148-83-0 is a valid CAS Registry Number.

22148-83-0Downstream Products

22148-83-0Relevant articles and documents

CYCLIZATION OF AMINYL RADICALS GENERATED BY ANODIC OXIDATION OF LITHIUM ALKENYLAMIDES. STEREO- AND REGIOSELECTIVE SYNTHESIS OF cis-1-ALKYL-2,5-DISUBSTITUTED PYRROLIDINES

Tokuda, Masao,Yamada, Yasufumi,Takagi, Toshiya,Suginome, Hiroshi,Furusaki, Akio

, p. 281 - 296 (1987)

Neutral aminyl radicals (3) generated by anodic oxidation of lithium alkenylamides (2) were found to undergo a stereo- and regioselective cyclization to give cis-1-alkyl-2,5-disubstituted pyrrolidines (5c-5h) in moderate yields.The cis stereochemistry of 5c-5h was confirmed by comparison with the corresponding trans-1-alkyl-2,5-disubstituted pyrrolidines which were prepared by aminomercuration of 1c-1h.The structure of trans-1,2-dimethyl-5-phenylpyrrolidine (17) was established by an X-ray crystallographic analysis of its ammonium bromide 21.Various aminyl radicals examined in this study were found to combine exclusively with the internal carbon of their double bond to give a five- (5a-5h) or six-membered ring (13).No product arising from the cyclization is obtained from N-methyl-1-phenylbut-3-enylamine (14).

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