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74619-81-1

(E)-N-(1,2-diphenylethyl)-1-phenylmethanimine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74619-81-1 Structure

  • Basic information

    1. Product Name: (E)-N-(1,2-diphenylethyl)-1-phenylmethanimine
    2. Synonyms:
    3. CAS NO:74619-81-1
    4. Molecular Formula:
    5. Molecular Weight: 285.389
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74619-81-1.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-(1,2-diphenylethyl)-1-phenylmethanimine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-N-(1,2-diphenylethyl)-1-phenylmethanimine(74619-81-1)
    11. EPA Substance Registry System: (E)-N-(1,2-diphenylethyl)-1-phenylmethanimine(74619-81-1)

  • 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: 74619-81-1(Hazardous Substances Data)

74619-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74619-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,1 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74619-81:
(7*7)+(6*4)+(5*6)+(4*1)+(3*9)+(2*8)+(1*1)=151
151 % 10 = 1
So 74619-81-1 is a valid CAS Registry Number.

74619-81-1Downstream Products

74619-81-1Relevant articles and documents

Photoorganocatalytic Aerobic Oxidative Amine Dehydrogenation/Super Acid-Mediated Pictet-Spengler Cyclization: Synthesis of cis-1,3-Diaryl Tetrahydroisoquinolines

Unkel, Lisa-Natascha,Malcherek, Simon,Schendera, Eva,Hoffmann, Frank,Rehbein, Julia,Brasholz, Malte

, p. 2870 - 2876 (2019)

Aerobic oxidative dehydrogenation reactions of benzylamines to imines were studied and the efficiencies of various ground- and excited state quinone organocatalysts were compared. Long wave-absorbing anthraquinones readily catalyze the aerobic photodehydr

The Reaction of Sodium 1,3-Diphenyl-2-azapropenide with 1,2-Epoxycyclohexane

Bradamante, Silvia,Ferraccioli, Raffaella,Pagani, Giorgio A.

, p. 515 - 518 (2007/10/02)

Ring opening of 1,2-epoxycyclohexane by the title aza-allylic anion afforded a mixture of anions, the quenching and subsequent hydrolysis of which gave rise to trans-2-(α-aminobenzyl)cyclohexanol (10) and benzylamine as the basic fraction, and to either 1-benzoylcyclohexene (11) or trans-2-benzoylcyclohexanol (12), cis-2-benzoylcyclohexanol (14), and benzaldehyde as the neutral fraction: the type of ketone obtained depended upon the hydrolytic conditions.The perhydrobenzoxazine (7) was shown to be the precursor of compound (10).Sodium 1,3-diphenyl-2-azapropenide thus behaved both as an α-benzylamine carbanion equivalent and as a benzoyl anion equivalent.

STEREOCHEMICAL INVESTIGATIONS. LI. STEREOCHEMICAL INVESTIGATION OF DERIVATIVES OF (-)-1,2-DIPHENYLETHYLAMINE

Potapov, V. M.,Dem'yanovich, V. M.,Solov'eva, L. D.,Vendrova, O. P.

, p. 683 - 686 (2007/10/02)

Optically active 1,2-diphenylethylamine was obtained, its optical purity was determined, and its configuration was confirmed by the circular dichroism (CD) method.

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