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3532-54-5

2-Benzylidene-3-oxo-N-phenylbutanamide is a complex organic compound with the molecular formula C17H15NO2. It is a derivative of butanamide, featuring a benzylidene group at the 2-position and a phenyl group at the nitrogen atom. The compound is characterized by a carbonyl group at the 3-position, which contributes to its reactivity and potential applications in chemical synthesis. It is often used as an intermediate in the preparation of various pharmaceuticals and other organic compounds due to its unique structure and reactivity.

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  • 3532-54-5 Structure

  • Basic information

    1. Product Name: 2-benzylidene-3-oxo-N-phenylbutanamide
    2. Synonyms: 2-benzylidene-3-oxo-N-phenylbutanamide
    3. CAS NO:3532-54-5
    4. Molecular Formula:
    5. Molecular Weight: 265.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3532-54-5.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: 2-benzylidene-3-oxo-N-phenylbutanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzylidene-3-oxo-N-phenylbutanamide(3532-54-5)
    11. EPA Substance Registry System: 2-benzylidene-3-oxo-N-phenylbutanamide(3532-54-5)

  • 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: 3532-54-5(Hazardous Substances Data)

3532-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3532-54-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3532-54:
(6*3)+(5*5)+(4*3)+(3*2)+(2*5)+(1*4)=75
75 % 10 = 5
So 3532-54-5 is a valid CAS Registry Number.

3532-54-5Relevant articles and documents

BF3·Et2O-mediated intramolecular cyclization of unsaturated amides: Convenient synthesis of dihydroquinolin-2-one-BF 2 complexes

Liu, Xu,Zhang, Qian,Xin, Xiaoqing,Zhang, Rui,Zhang, Ning,Liang, Yongjiu,Dong, Dewen

, p. 36234 - 36240 (2014)

A facile and efficient synthesis of substituted dihydropyridone-BF 2 complexes is developed via intramolecular cyclization of α-acyl acrylamides and α-acyl cinnamamides mediated by BF 3·Et2O. This journal is the Partner Or

Triflic Anhydride Promoted Intramolecular Cyclization of N -Aryl Cinnamides: Access to Polysubstituted Quinolin-2(1 H)-ones

Zhang, Qian,Yuan, Jingwen,Yu, Mangfei,Zhang, Rui,Liang, Yongjiu,Huang, Peng,Dong, Dewen

, p. 4996 - 5002 (2017/10/06)

A facile and efficient synthesis of polysubstituted quinolin-2(1 H)-ones is developed via intramolecular cyclization of readily available N -aryl cinnamides promoted by triflic anhydride in N, N -dimethyl trifluoroacetamide (DTA) under mild conditions.

PPA-mediated C-C bond formation: A synthetic route to substituted indeno[2,1-c]quinolin-6(7 H)-ones

Liu, Xu,Zhang, Qian,Zhang, Dingyuan,Xin, Xiaoqing,Zhang, Rui,Zhou, Fenguo,Dong, Dewen

supporting information, p. 776 - 779 (2013/04/10)

A facile and efficient synthesis of substituted indeno[2,1-c]quinolin-6(7H) -ones from a variety of α-acyl N-arylcinnamamides mediated by polyphosphoric acid (PPA) is described, and a mechanism involving the formation of a dicationic superelectrophile and

PYRROLE COMPOUNDS AND USES THEREOF

-

Page/Page column 50, (2010/11/24)

Pyrrole compounds, compositions and methods are provided for the treatment, prevention, or amelioration of neurodegenerative diseases, cardiovascular diseases, proliferative diseases and visual disorders. In particular, pyrrole compounds, compositions and methods for the treatment of stroke are disclosed herein.

Synthesis of New Anilidopyrimidinethione Derivatives

Khalil, Zarif H.,Yanni, Amal S.

, p. 494 - 497 (2007/10/02)

Interaction of acetoacetanilide (Ia) or its hydroxy derivative (Ib) with aromatic or heterocyclic aldehydes gave the corresponding α, β unsaturated ketones (II).The reaction of alcoholic solution of (II) with thiourea in a basic catalyst gave the corresponding pyrimidinethione derivatives (III).Fusion of (III) with amines, active methylene, and methyl compounds gave the corresponding condensation products IV, V, and VI.

Synthesis of New Anilido-Pyrazoline and Isoxazoline Derivatives

Khali, Zarif A.,Yanni, Amal S.

, p. 168 - 170 (2007/10/02)

Interaction of acetoacetanilide(Ia) or its hydroxy derivative(Ib) with aromatic (or heterocyclic) aldehydes gave the corresponding α,β-unsaturated ketones(II).The reaction of alcoholic solution of (II) with hydrazine hydrate or hydroxylamine in a basic ca

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