154323-99-6 Usage
Structure
Thiazole derivative with a carbohydrazide functional group and a thienyl group attached to the thiazole ring
Biological activities
Potential antifungal and antibacterial properties
Potential uses
As an antifungal agent, for inhibiting the growth of certain bacteria, and in materials science for the development of new polymers or as a building block for the synthesis of larger molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 154323-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,3,2 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 154323-99:
(8*1)+(7*5)+(6*4)+(5*3)+(4*2)+(3*3)+(2*9)+(1*9)=126
126 % 10 = 6
So 154323-99-6 is a valid CAS Registry Number.
154323-99-6Relevant articles and documents
Synthesis and phototoxicity of some 2--1,3,4-oxa or thiadiazoles and 3--1,2,4-triazolin-5-thiones
Singh, S. P.,Ranjana
, p. 1130 - 1136 (2007/10/02)
2-Acyl-1-hydrazines (4), obtained from 2-(2-thienyl)-4-thiazole carbohydrazide (3) and acid chlorides, were cyclized with PPA and P2S5 separately to 5-alkyl-2--1,3,4-oxa and thiadiazoles (6,7), respectively.The thiosemicarbazides (5), obtained from reaction of 3 and alkyl isothiocyanates, on cyclodehydration with I2/NaOH and conc.H2SO4 separately furnish 5-alkylamino-2--1,3,4-oxa and thiadiazoles (8 and 9), respectively.Refluxing 5 in dil NaOH, however, provide 4-alkyl--1,2,4-triazolin-5-thiones (10).The NMR (1H and 13C) and mass spectral characteristics of these compounds are also reported.
