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2-Azetidinone, 1-methyl-3-[(1-methyl-5-nitro-1H-imidazol-2-yl)methylene]-4-phenyl-, (Z)- is a complex organic compound with the molecular formula C15H14N4O3. It features a 2-azetidinone core, which is a four-membered cyclic amide, and is characterized by the presence of a methyl group at the 1-position. The compound also contains a 1-methyl-5-nitro-1H-imidazol-2-yl group that forms a methylene bridge with the 3-position of the azetidinone ring, and a phenyl group at the 4-position. The (Z)- configuration indicates the geometric arrangement of the double bond in the molecule, which is crucial for its stereochemistry. 2-Azetidinone, 1-methyl-3-[(1-methyl-5-nitro-1H-imidazol-2-yl)methylene]-4-phenyl-, (Z)- is known for its potential applications in pharmaceuticals and as a chemical intermediate, particularly in the synthesis of certain drugs.

123794-15-0

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123794-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123794-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,7,9 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 123794-15:
(8*1)+(7*2)+(6*3)+(5*7)+(4*9)+(3*4)+(2*1)+(1*5)=130
130 % 10 = 0
So 123794-15-0 is a valid CAS Registry Number.

123794-15-0SDS

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 1-methyl 2-(1-methyl 4-phenyl azetidin-2-one 3-ylidenemethyl) 5-nitroimidazole (Z)

1.2 Other means of identification

Product number -
Other names 1-Methyl-3-[1-(1-methyl-5-nitro-1H-imidazol-2-yl)-meth-(Z)-ylidene]-4-phenyl-azetidin-2-one

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:123794-15-0 SDS

123794-15-0Downstream Products

123794-15-0Relevant academic research and scientific papers

New 5-nitroimidazoles bearing lactame nucleus: Synthesis and antibacterial properties

Jentzer,Vanelle,Crozet,Maldonado,Barreau

, p. 687 - 697 (2007/10/02)

New 5-nitroimidazoles bearing a trisubstituted ethylenic double bond in position 2 were prepared by reacting various 1-alkyl-2-chloromethyl-5-nitroimidazole with 3-nitrolactam anions by S(RN)1 mechanism in phase-transfer catalysis conditions. These compounds showed in vitro and in vivo antianaerobic activity which was clearly greater than that of metronidazole. Structure-activity relationships have been discussed.

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