130111-89-6 Usage
Chemical class
Thiazolidine class of organic compounds
Structural features
Contains a thiazolidine ring with a phenyl substituent at the 2-position and a thiourea group at the 3-position
Derivative type
Thiourea derivative
Common use
Organic synthesis and pharmaceutical research
Applications
Potential applications in drug development
Structural importance
Valuable building block for the synthesis of various bioactive molecules and pharmaceuticals
Pharmacological activities
Investigated for anti-inflammatory and antioxidant properties
These properties and specific content provide a comprehensive overview of 1-(4-oxo-2-phenyl-1,3-thiazolidin-3-yl)thiourea, highlighting its chemical structure, common uses, and potential applications in the field of pharmaceutical research and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 130111-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,1 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130111-89:
(8*1)+(7*3)+(6*0)+(5*1)+(4*1)+(3*1)+(2*8)+(1*9)=66
66 % 10 = 6
So 130111-89-6 is a valid CAS Registry Number.
130111-89-6Relevant articles and documents
One-pot synthesis of 2-amino-5-aryl-5H-thiazolo[4,3-b]-1,3,4-thiadiazoles
Shukurov,Kukaniev,Alibaeva
, p. 724 - 725 (1996)
Equimolar mixtures of aromatic aldehydes with thioglycolic acid and thiosemicarbazide in H2SO4 transform into 2-amino-5-aryl-5H-thiazolo[4,3-b]-1,3,4-thiadiazoles.
New Fungitoxic Fused-Ring Synthetics Incorporating Azoles and Azines in Different Combinations
Yadav, Lal Dhar S.,Vaish, Anjum,Sharma, Sangeeta
, p. 811 - 813 (2007/10/02)
2-Aryl-3-thioureido-4-thiazolidinones IIa,b obtained by addition-condensation of aldehyde thiosemicarbazones Ia,b and mercaptoacetic acid underwent chemoselective intramolecular heterocyclizations to 5-aryl-2-mercapto-1,5-dihydrothiazolo-1,2,4-tria
