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N-Benzyl-4-[4-methyl-5-oxo-1,5-dihydro-pyrrol-(2Z)-ylidene]-butyramide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 215106-54-0 Structure
  • Basic information

    1. Product Name: N-Benzyl-4-[4-methyl-5-oxo-1,5-dihydro-pyrrol-(2Z)-ylidene]-butyramide
    2. Synonyms: N-Benzyl-4-[4-methyl-5-oxo-1,5-dihydro-pyrrol-(2Z)-ylidene]-butyramide
    3. CAS NO:215106-54-0
    4. Molecular Formula:
    5. Molecular Weight: 270.331
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 215106-54-0.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-Benzyl-4-[4-methyl-5-oxo-1,5-dihydro-pyrrol-(2Z)-ylidene]-butyramide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Benzyl-4-[4-methyl-5-oxo-1,5-dihydro-pyrrol-(2Z)-ylidene]-butyramide(215106-54-0)
    11. EPA Substance Registry System: N-Benzyl-4-[4-methyl-5-oxo-1,5-dihydro-pyrrol-(2Z)-ylidene]-butyramide(215106-54-0)
  • 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: 215106-54-0(Hazardous Substances Data)

215106-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215106-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,1,0 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 215106-54:
(8*2)+(7*1)+(6*5)+(5*1)+(4*0)+(3*6)+(2*5)+(1*4)=90
90 % 10 = 0
So 215106-54-0 is a valid CAS Registry Number.

215106-54-0Downstream Products

215106-54-0Relevant articles and documents

Synthesis of azaspiro[4.5]decane systems by oxidative cyclization of olefinic precursors

Martin-Lopez, Maria J.,Bermejo, Francisco

, p. 12379 - 12388 (2007/10/03)

The synthesis of 6-benzyloxycarbonyl-1-oxa-6-azaspiro[4.5]decan-2-one (17) and 6-benzyloxycarbonyl-1,6-diazaspiro[4.5]decan-2-one (18) from the D,L-pipecolic acid derivative 10, is described. The synthesis of (±)-6- benzyl-3-methyl-1,6-diazaspiro[4.5]dec-3-ene-2,7-dione (29), the spiro structural unit of (±)-pandamarine (8) has been achieved by oxidative cyclization of the (Z) and (E) isomers of 5-(N-benzyl-4- carboxamidobutylidene)-3-methyl-3-pyrrolin-2-one (25) and (26). The stereoselectivity obtained in the intramolecular cyclization process has also been discussed.

Synthesis of α,β-Unsaturated Spirolactams by Intramolecular Cyclization of Endocyclic N-Acyliminium Ions

Martin, Maria J.,Bermejo, Francisco

, p. 7705 - 7708 (2007/10/02)

The synthesis of (+/-)-6-benzyl-3-methyl-3-en-1,6-diazaspirodecane-2,7-dione (18), the spiro moiety of (+/-)-pandamarine has been achieved by oxidative cyclization of the (Z) and (E) isomers of 5-(N-benzyl-4-carboxamido-butylidene)-3-methyl-3-en-pyrrolin-2-one (15a) and (15b).The stereoselectivity exhibited in the intramolecular cyclization by both butylidene precursors has also been discussed.

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