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(E)-3-{[1-Phenyl-meth-(E)-ylidene]-amino}-but-2-enal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74328-26-0 Structure
  • Basic information

    1. Product Name: (E)-3-{[1-Phenyl-meth-(E)-ylidene]-amino}-but-2-enal
    2. Synonyms: (E)-3-{[1-Phenyl-meth-(E)-ylidene]-amino}-but-2-enal
    3. CAS NO:74328-26-0
    4. Molecular Formula:
    5. Molecular Weight: 173.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74328-26-0.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: (E)-3-{[1-Phenyl-meth-(E)-ylidene]-amino}-but-2-enal(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-{[1-Phenyl-meth-(E)-ylidene]-amino}-but-2-enal(74328-26-0)
    11. EPA Substance Registry System: (E)-3-{[1-Phenyl-meth-(E)-ylidene]-amino}-but-2-enal(74328-26-0)
  • 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: 74328-26-0(Hazardous Substances Data)

74328-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74328-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,2 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74328-26:
(7*7)+(6*4)+(5*3)+(4*2)+(3*8)+(2*2)+(1*6)=130
130 % 10 = 0
So 74328-26-0 is a valid CAS Registry Number.

74328-26-0Downstream Products

74328-26-0Relevant articles and documents

REARRANGEMENTS SIGMATROPIQUES ET DIMERISATION D'α-IMINOCETENES ENGENDRES PAR THERMOLYSE D'ENAMINOESTERS

Maujean,Marcy,Chuche

, p. 519 - 522 (2007/10/02)

α-Iminoketenes derived from thermolysis of enaminoesters yield azadienals by sigmatropic hydrogen shift and dimerization products by cycloaddition

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