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56158-78-2

4(3H)-Quinazolinone, 2-phenyl-3-[(3-phenyl-2-propenylidene)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56158-78-2 Structure

  • Basic information

    1. Product Name: 4(3H)-Quinazolinone, 2-phenyl-3-[(3-phenyl-2-propenylidene)amino]-
    2. Synonyms:
    3. CAS NO:56158-78-2
    4. Molecular Formula: C23H17N3O
    5. Molecular Weight: 351.407
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56158-78-2.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: 4(3H)-Quinazolinone, 2-phenyl-3-[(3-phenyl-2-propenylidene)amino]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4(3H)-Quinazolinone, 2-phenyl-3-[(3-phenyl-2-propenylidene)amino]-(56158-78-2)
    11. EPA Substance Registry System: 4(3H)-Quinazolinone, 2-phenyl-3-[(3-phenyl-2-propenylidene)amino]-(56158-78-2)

  • 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: 56158-78-2(Hazardous Substances Data)

56158-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56158-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,5 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56158-78:
(7*5)+(6*6)+(5*1)+(4*5)+(3*8)+(2*7)+(1*8)=142
142 % 10 = 2
So 56158-78-2 is a valid CAS Registry Number.

56158-78-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(cinnamylideneamino)-2-phenylquinazolin-4-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56158-78-2 SDS

56158-78-2Downstream Products

56158-78-2Relevant articles and documents

Synthesis, Antimicrobial and Anticancer Evaluation of 2-Azetidinones Clubbed with Quinazolinone

Deep, Aakash,Kumar, Pradeep,Narasimhan, Balasubrmanian,Meng, Lim Siong,Ramasamy, Kalavathy,Mishra, Rakesh Kumar,Mani, Vasudevan

, p. 24 - 28 (2016/07/26)

A novel series of 2-azetidinones clubbed with quinazolinone was synthesized using anthranilic acid. All the synthesized compounds were evaluated for their antimicrobial activity against two Gram positive bacterial strains (Bacillus subtilis and Staphyloco

Synthesis and pharmacological investigation of some novel 2,3-disubstituted quinazolin-4(3H)-ones as analgesic and antiinflammatory agents

Alagarsamy,Meena,Vijayakumar,Ramseshu,Revathi

, p. 233 - 236 (2007/10/03)

A series of novel 2-substituted quinazolin-4(3H)-ones have been synthesized by condensing the aromatic primary amine of 2-substituted quinazolines with different aldehydes and ketones. The synthesized compounds were confirmed by their spectral data (IR, N

Synthesis of certain 3-aminoquinazolinone Schiff's bases structurally related to some biologically active compounds.

Roshdy,Ghoneim,Khalifa

, p. 210 - 213 (2007/10/08)

The condensation of 2-methyl-3-amino-4(3H)-quinazolinone and 2-phenyl-3-amino-4(3H)-quinazolinone with different aldehydes is described. Reacting equimolecular amounts of these two amino compounds with p-nitrobenzaldehyde, p-hydroxybenzaldehyde, cinnamaldehyde and 5-nitro-2-furfuraldehyde diacetate afforded the respective Schiff's bases. Condensation of benzaldehyde, anisaldehyde, p-dimethylaminobenzaldehyde and o-nitrobenzaldehyde with the former quinazolinone afforded the corresponding condensation products while with the latter no condensation took place. Furthermore, condensation of cinnamaldehyde with methylaminoquinazolinone in pyridine and in glacial acetic acid afforded the mono- and di-condensation products respectively while furfural, thiophenaldehyde, resorcinaldehyde, protocatechualdehyde, veratraldehyde, and salicylaldehyde, the condensation ended in failure.

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