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cis-3-chloro-4-methyl-1-phenylpyrrolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122278-39-1 Structure
  • Basic information

    1. Product Name: cis-3-chloro-4-methyl-1-phenylpyrrolidin-2-one
    2. Synonyms:
    3. CAS NO:122278-39-1
    4. Molecular Formula:
    5. Molecular Weight: 209.675
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122278-39-1.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: cis-3-chloro-4-methyl-1-phenylpyrrolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: cis-3-chloro-4-methyl-1-phenylpyrrolidin-2-one(122278-39-1)
    11. EPA Substance Registry System: cis-3-chloro-4-methyl-1-phenylpyrrolidin-2-one(122278-39-1)
  • 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: 122278-39-1(Hazardous Substances Data)

122278-39-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122278-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,2,7 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122278-39:
(8*1)+(7*2)+(6*2)+(5*2)+(4*7)+(3*8)+(2*3)+(1*9)=111
111 % 10 = 1
So 122278-39-1 is a valid CAS Registry Number.

122278-39-1Downstream Products

122278-39-1Relevant articles and documents

Radical cyclizations in 1,4-dimethylpiperazine

Ishibashi, Hiroyuki,Haruki, Shigeki,Uchiyama, Masahiko,Tamura, Osamu,Matsuo, Jun-ichi

, p. 6263 - 6266 (2006)

N-Allylic or N-vinylic α,α,α-trichloroacetamides, upon heating in 1,4-dimethylpiperazine, undergo radical cyclization to give the corresponding γ-lactams.

Synthesis of α-Chlorolactams by Cyanoborohydride-Mediated Radical Cyclization of Trichloroacetamides

Coussanes, Guilhem,Jakobi, Harald,Lindell, Stephen,Bonjoch, Josep

supporting information, p. 8151 - 8156 (2018/05/30)

A cyanoborohydride-promoted radical cyclization methodology has been developed to access α-chlorolactams in a simple and efficient way using NaBH3CN and trichloroacetamides easily available from allylic and homoallylic secondary amines. This methodology allowed the synthesis of a library of α-chlorolactams (mono- and bicyclic), which were tested for herbicidal activity, trans-3-chloro-4-methyl-1-(3-trifluoromethyl)phenyl-2-pyrrolidinone being the most active.

Synthesis of Five-membered Lactams by α-Carbamoyl Radical Cyclisations

Sato, Tatsunori,Wada, Yasuko,Nishimoto, Mami,Ishibashi, Hiroyuki,Ikeda, Masazumi

, p. 879 - 886 (2007/10/02)

Free-radical cyclisation of N-allyl-α-carbamoyl radicals generated by tributyltin radical-mediated cleavage of carbon-chlorine or carbon-sulphur bonds has been studied in some detail.The radicals substituted at the α position by methylthio (phenylthio), c

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