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2-Propenoic acid, 3-phenyl-, 2-[(2-chlorophenyl)methylene]hydrazide is a complex organic compound with the chemical formula C16H13ClN2O2. It is a derivative of 2-propenoic acid, featuring a phenyl group at the 3-position and a hydrazide group at the 2-position. The hydrazide group is further substituted with a 2-chlorophenyl group, which forms a methylene bridge with the hydrazide nitrogen. 2-Propenoic acid,3-phenyl-, 2-[(2-chlorophenyl)methylene]hydrazide is characterized by its unique molecular structure, which includes a double bond in the propenoic acid backbone, a phenyl ring, and a chlorophenyl group attached to the hydrazide. It is a white to off-white crystalline solid and is used in the synthesis of various pharmaceuticals and chemical intermediates. Due to its complex structure and potential reactivity, it is important to handle 2-Propenoic acid,3-phenyl-, 2-[(2-chlorophenyl)methylene]hydrazide with care, following appropriate safety protocols.

25330-03-4

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25330-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25330-03-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25330-03:
(7*2)+(6*5)+(5*3)+(4*3)+(3*0)+(2*0)+(1*3)=74
74 % 10 = 4
So 25330-03-4 is a valid CAS Registry Number.

25330-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-N-[(E)-(2-chlorophenyl)methylideneamino]-3-phenylprop-2-enamide

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:25330-03-4 SDS

25330-03-4Downstream Products

25330-03-4Relevant academic research and scientific papers

Benzylidene/2-chlorobenzylidene hydrazides: Synthesis, antimicrobial activity, QSAR studies and antiviral evaluation

Kumar, Davinder,Judge, Vikramjeet,Narang, Rakesh,Sangwan, Sonia,De Clercq, Erik,Balzarini, Jan,Narasimhan, Balasubramanian

experimental part, p. 2806 - 2816 (2010/08/20)

A series of benzylidene hydrazides (1-20) was synthesized and tested, in vitro, for antibacterial, antifungal and antiviral activities. The microbial screening results indicated that compounds having chloro and nitro substituents were the most active ones. The antiviral evaluation depicted that compounds 9 and 19 were active against Vesicular stomatitis virus (VSV) in HeLa cell cultures. QSAR investigations indicated that the multi-target QSAR model was effective in describing the antimicrobial (antibacterial and antifungal) activity over the one-target QSAR models. Further the mt-QSAR model indicated that the topological parameters, second order molecular connectivity index (2χ) and third order Kier's alpha shape index (κα3) are effective in describing the antimicrobial activity of synthesized hydrazides.

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