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CAS

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64859-04-7

(E)-N-cinnamylideneaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64859-04-7 Structure

  • Basic information

    1. Product Name: (E)-N-cinnamylideneaniline
    2. Synonyms: (E)-N-cinnamylideneaniline
    3. CAS NO:64859-04-7
    4. Molecular Formula:
    5. Molecular Weight: 207.275
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64859-04-7.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-cinnamylideneaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-N-cinnamylideneaniline(64859-04-7)
    11. EPA Substance Registry System: (E)-N-cinnamylideneaniline(64859-04-7)

  • 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: 64859-04-7(Hazardous Substances Data)

64859-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64859-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,5 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64859-04:
(7*6)+(6*4)+(5*8)+(4*5)+(3*9)+(2*0)+(1*4)=157
157 % 10 = 7
So 64859-04-7 is a valid CAS Registry Number.

64859-04-7Relevant articles and documents

HBF4 catalyzed Mannich-type reaction in aqueous media

Akiyama, Takahiko,Takaya, Jun,Kagoshima, Hirotaka

, p. 1045 - 1048 (1999)

HBF4 catalyzed Mannich-type reaction took place smoothly in aqueous media to afford β-amino carbonyl compounds in high yields. One-pot synthesis of β-amino carbonyl compounds from aldehyde and amine also worked well.

Oxidation of various secondary amines to imines with N-tert-butylphenylsulfinimidoyl chloride

Mukaiyama, Teruaki,Kawana, Asahi,Fukuda, Yoshio,Matsuo, Jun-Ichi

, p. 390 - 391 (2007/10/03)

Various secondary amines were smoothly oxidized to the corresponding imines at -78 °C by using N-tert-butylphenylsulfinimidoyl chloride and DBU.

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