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1394171-55-1

(E)-N-(3-methylpent-3-en-2-yl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1394171-55-1 Structure

  • Basic information

    1. Product Name: (E)-N-(3-methylpent-3-en-2-yl)aniline
    2. Synonyms: (E)-N-(3-methylpent-3-en-2-yl)aniline
    3. CAS NO:1394171-55-1
    4. Molecular Formula:
    5. Molecular Weight: 175.274
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1394171-55-1.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: (E)-N-(3-methylpent-3-en-2-yl)aniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-N-(3-methylpent-3-en-2-yl)aniline(1394171-55-1)
    11. EPA Substance Registry System: (E)-N-(3-methylpent-3-en-2-yl)aniline(1394171-55-1)

  • 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: 1394171-55-1(Hazardous Substances Data)

1394171-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1394171-55-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,1,7 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1394171-55:
(9*1)+(8*3)+(7*9)+(6*4)+(5*1)+(4*7)+(3*1)+(2*5)+(1*5)=171
171 % 10 = 1
So 1394171-55-1 is a valid CAS Registry Number.

1394171-55-1Upstream product

1394171-55-1Relevant articles and documents

A modular approach to α,β-unsaturated N-aryl ketonitrones

Hood, Tyler S.,Bryan Huehls,Yang, Jiong

, p. 4679 - 4682 (2012)

A modular approach to α,β-unsaturated N-aryl ketonitrones has been developed. Specifically, condensation of anilines and enals followed by alkylation of the resulting α,β-unsaturated imines provided N-allyl anilines, which were subjected to oxidation with

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