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4-{[(E)-(3-nitrophenyl)methylidene]amino}phenol is an organic compound characterized by its chemical structure, which features a phenol group (C6H4OH) with a nitro group (NO2) attached to the 3rd position of the phenyl ring. The molecule also contains an amino group (NH2) connected to the 4th position of the phenyl ring, which is further linked to a methylene group (CH2) that forms a double bond with the nitrophenyl group, creating an E-configuration. 4-{[(E)-(3-nitrophenyl)methylidene]amino}phenol is known for its potential applications in the synthesis of dyes and pharmaceuticals, and it is also recognized for its distinct chemical properties, such as its reactivity and stability.

5348-27-6

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5348-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5348-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5348-27:
(6*5)+(5*3)+(4*4)+(3*8)+(2*2)+(1*7)=96
96 % 10 = 6
So 5348-27-6 is a valid CAS Registry Number.

5348-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(3-nitrophenyl)methylideneamino]phenol

1.2 Other means of identification

Product number -
Other names N-<3-Nitro-benzyliden>-4-hydroxy-anilin

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:5348-27-6 SDS

5348-27-6Downstream Products

5348-27-6Relevant academic research and scientific papers

Evaluation of antibacterial activity of some Schiff bases

Baluja, Shipra,Parikh, Jigna,Chanda, Sumitra,Vaishnani

experimental part, p. 1338 - 1342 (2010/08/05)

From 4-amino phenol, some Schiff bases were synthesized. By IR and NMR spectral data, the structural characterization of these synthesized compounds were done. The antibacterial activity of all these synthesized Schiff bases was studied against B. cereus-ATCC 11778, P. aero-ATCC 27853, E. coli-ATCC 25922, K pneu-NCIM 2719 and 5. aureus-ATCC 25923, by agar ditch method in dimethyl formamide and dimethyl sulfoxide. It is observed that antibacterial activity depends on the molecular structure of Schiff base, solvent used and bacterial strain under consideration. Out of two solvents studied, dimethyl formamide is proved to be best and salicylaldehyde as side chain to 4-amino phenol could be used as lead molecule in drug designing i.e. in inhibiting above bacterial strains.

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