32084-55-2 Usage
General Description
5-OXO-2,3-DIHYDRO-5H-PYRIMIDO[2,1-B][1,3]THIAZOLE-6-CARBOXYLIC ACID is a chemical compound with a complex molecular structure. It contains a pyrimidine ring fused with a thiazole ring, as well as a carboxylic acid functional group. The compound is a heterocyclic compound, meaning it contains atoms of at least two different elements in its ring structure. It is also a ketone, as indicated by the "5-OXO" prefix in its name. This chemical may have potential applications in pharmaceuticals, agricultural products, or other industrial processes due to its unique structure and properties. However, further research and analysis would be necessary to determine its specific uses and potential effects.
Check Digit Verification of cas no
The CAS Registry Mumber 32084-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,0,8 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 32084-55:
(7*3)+(6*2)+(5*0)+(4*8)+(3*4)+(2*5)+(1*5)=92
92 % 10 = 2
So 32084-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O3S/c10-5-4(6(11)12)3-8-7-9(5)1-2-13-7/h3H,1-2H2,(H,11,12)/p-1
32084-55-2Relevant articles and documents
Synthesis & Biological Activity of Some New Carboxamides, Carbohydrazides & Carbamates Derived from 2,3-Dihydro-5(H)-oxothiazolopyrimidine-6-carboxylic Acid
Shridhar, D. R.,Jogibhukta, M.,Joshi, P. P.,Rao, C. Seshagiri,Junnarkar, A. Y.
, p. 492 - 494 (2007/10/02)
Some new carboxamides (Va-j), carbohydrazides (Vk-p) and carbamates (VIIIa-d) derived from 2,3-dihydro-5(H)-oxothiazolopyrimidine-6-carboxylic acid (III) have been synthesised and evaluated for their antiinflammatory, antibacterial, antifungal and anthelmintic activities.The carboxamides (Ve,i,j) and carbohydrazides (Vk,n,o) possess promising antiinflammatory activity against carrageenin-induced paw oedema in rats, compound Ve being the most active member of the series showing 50.8 percent inhibition at 200 mg/kg (p.o.) dose.Ve, however, is found to be inactive at lower doses.None of the compounds shows any noteworthy antibacterial, antifungal or anthelmintic activities except Vk which displays promising antitubercular activity in vitro (MIC=5 mcg/ml) against Mycobacterium tuberculosis H37Rv.
