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Ethyl (2Z)-2-{[5-(4-chlorophenyl)furan-2-yl]methylidene}-7-methyl-5-(4-methylphenyl)-3-oxo-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate is a complex organic compound with a molecular formula of C27H22ClN3O4S. It is characterized by a [1,3]thiazolo[3,2-a]pyrimidine core, which is a heterocyclic ring system containing sulfur and nitrogen. The molecule features a 2,3-dihydro structure, indicating the presence of two hydrogen atoms attached to the ring, and a 3-oxo group, which is a carbonyl group (C=O) at the 3-position. The compound also includes a 7-methyl group, a 5-(4-methylphenyl) substituent, and a 5-(4-chlorophenyl)furan-2-yl group, which contributes to its overall structure and potential biological activity. The ethyl carboxylate group at the 6-position suggests that ethyl (2Z)-2-{[5-(4-chlorophenyl)furan-2-yl]methylidene}-7-methyl-5-(4-methylphenyl)-3-oxo-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate may have ester-like properties. This chemical is likely to be of interest in medicinal chemistry due to its potential as a precursor or intermediate in the synthesis of pharmaceuticals, given its complex structure and the presence of multiple functional groups that can interact with biological targets.

5669-90-9

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5669-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5669-90-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5669-90:
(6*5)+(5*6)+(4*6)+(3*9)+(2*9)+(1*0)=129
129 % 10 = 9
So 5669-90-9 is a valid CAS Registry Number.

5669-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (2Z)-2-[[5-(4-chlorophenyl)furan-2-yl]methylidene]-7-methyl-5-(4-methylphenyl)-3-oxo-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate

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

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More Details:5669-90-9 SDS

5669-90-9Downstream Products

5669-90-9Relevant academic research and scientific papers

Aqueous phase synthesis, crystal structure and antimicrobial activity of 4-(substituted phenylazo)-3-methyl-4H-isoxazol-5-one azo dyes

Banpurkar, Anita R.,Wazalwar, Sachin S.,Perdih, Franc

, p. 249 - 257 (2018)

3-Methyl-4H-isoxazol-5-one was synthesized at room temperature by simple stirring method from ethyl acetoacetate and hydroxylamine hydrochloride in aqueous medium and coupled with diazotized substituted amine to form series of 4-(substituted phenylazo)-3-methyl-4H-isoxazol-5-ones through green chemistry. All the compounds formed were characterized by IR, 1H and 13C NMR spectroscopy, MS and elemental analysis. Crystal structure of novel 4-(4-fluorophenylazo)-3-methyl-4H-isoxazol-5-one was determined by the X-ray diffraction. Antibacterial and antifungal activity was studied against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus pyogenus and Candida albicans, Aspergillus niger, Aspergillus clavatus, respectively. All synthesized compounds were found to be active against a gram-positive bacterium Staphylococcus aureus. Two compounds showed antifungal activity against Candida albicans close to standard greseofulvin.

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