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389621-14-1

Benzenemethanamine, N-[[1-(3-methyl-2-butenyl)-1H-pyrrol-2-yl]methylene]-, N-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Benzenemethanamine, N-[[1-(3-methyl-2-butenyl)-1H-pyrrol-2-yl]methylene]-, N-oxide

    Cas No: 389621-14-1

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  • 389621-14-1 Structure

  • Basic information

    1. Product Name: Benzenemethanamine, N-[[1-(3-methyl-2-butenyl)-1H-pyrrol-2-yl]methylene]-, N-oxide
    2. Synonyms:
    3. CAS NO:389621-14-1
    4. Molecular Formula: C17H20N2O
    5. Molecular Weight: 268.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 389621-14-1.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: Benzenemethanamine, N-[[1-(3-methyl-2-butenyl)-1H-pyrrol-2-yl]methylene]-, N-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanamine, N-[[1-(3-methyl-2-butenyl)-1H-pyrrol-2-yl]methylene]-, N-oxide(389621-14-1)
    11. EPA Substance Registry System: Benzenemethanamine, N-[[1-(3-methyl-2-butenyl)-1H-pyrrol-2-yl]methylene]-, N-oxide(389621-14-1)

  • 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: 389621-14-1(Hazardous Substances Data)

389621-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 389621-14-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,6,2 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 389621-14:
(8*3)+(7*8)+(6*9)+(5*6)+(4*2)+(3*1)+(2*1)+(1*4)=181
181 % 10 = 1
So 389621-14-1 is a valid CAS Registry Number.

389621-14-1Relevant articles and documents

Regiochemical aspects of intramolecular cycloadditions of nitrones derived from N-(2-alkenyl)-2-pyrrolecarbaldehydes. Competitive entries to pyrrolizidine and indolizidine derivatives

Broggini, Gianluigi,La Rosa, Concetta,Pilati, Tullio,Terraneo, Alberto,Zecchi, Gaetano

, p. 8323 - 8332 (2001)

Intramolecular cycloadditions of unsaturated nitrones derived from a series of N-(2-alkenyl)-2-pyrrolecarbaldehydes (2) have been systematically studied. A pronounced substituent effect has been observed as far as the competitive formation of fused- and bridged-ring regioisomers are concerned. Further elaboration of the two kinds of cycloadducts has given pyrrolizidine and indolizidine derivatives, respectively.

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