Welcome to LookChem.com Sign In|Join Free
  • or
2-(4-methoxy)phenyl-4-(thiophen-2-ylmethylene)-5-oxazolinone is a complex organic compound with the molecular formula C15H11NO3S. It features a 5-oxazolinone core, which is a heterocyclic ring system consisting of an oxazolidinone ring fused with a pyrrolidinone ring. The compound has a 4-methoxyphenyl group attached to the 2-position of the oxazolinone, which introduces a methoxy substituent that can influence the electronic properties of the molecule. Additionally, a thiophene-2-ylmethylene group is attached to the 4-position, providing a sulfur-containing aromatic ring that can contribute to the compound's reactivity and stability. This specific arrangement of functional groups may endow the molecule with unique chemical and physical properties, making it potentially useful in various applications, such as in pharmaceuticals or materials science.

4211-92-1

Post Buying Request

4211-92-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

4211-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4211-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,1 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4211-92:
(6*4)+(5*2)+(4*1)+(3*1)+(2*9)+(1*2)=61
61 % 10 = 1
So 4211-92-1 is a valid CAS Registry Number.

4211-92-1Downstream Products

4211-92-1Relevant academic research and scientific papers

Synthesis, characterization and anticancer activity of (5,1-substituted)-3-(indoline-4-(thiophene- 2-yl-methylene)-2-(p-tolyl)-2-methylene)-4,3-dihydro-1h-imidazole-5-one derivatives

BAYYA, CHANDRAPRAKASH,MANDA, SARANGAPANI

, p. 2027 - 2032 (2021/08/24)

The synthesis of novel imidazole-5-one derivatives (5a-j) was allowed in a conventional method by way of Erlenmeyer and Schiff base mechanism. Compound 2a was synthesized by Erlenmeyer reaction of N-(4-methoxy benzoyl)glycine with 2-thiophene-carboxaldehyde in the presence of acetic anhydride and anhydrous sodium acetate. Finally, it undergoes dehydration reaction with Schiff bases of isatin derivatives (4a-j) to yield final compounds 5a-j. The organic potentials of the newly synthesized imidazole-5-one derivatives have been evaluated for their in vitro anticancer activity by MTT assay method. It against MCF-7 cells as comparison with doxorubicin popular drug. The synthesized compounds 5e, 5f and 5j exhibited excellent anticancer activity against MCF-7 cell lines.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 4211-92-1