141542-11-2 Usage
Chemical structure
A complex structure containing a thiadiazole ring, an amine group at position 3, a 1,1-dioxide functional group at position 4,5, and a 4-methylphenyl group attached to the thiadiazole ring.
Functional groups
Thiadiazole ring, amine group, 1,1-dioxide functional group, and 4-methylphenyl group.
Potential applications
The compound may have potential applications in pharmaceuticals, agrochemicals, or material science due to its unique structure and properties.
Further research
Additional research and study may be needed to fully understand and utilize the potential of this compound.
Physical state
The physical state of the compound is not provided in the material, but it is likely a solid at room temperature, as many organic compounds with complex structures are.
Solubility
The solubility of the compound is not provided in the material, but it may be soluble in organic solvents such as ethanol, methanol, or acetone, depending on its polarity and molecular interactions.
Stability
The stability of the compound is not provided in the material, but it may be sensitive to heat, light, or moisture, as many organic compounds with complex structures are.
Reactivity
The reactivity of the compound is not provided in the material, but it may react with strong acids, strong bases, or other reactive chemicals, depending on the reactivity of its functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 141542-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,4 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 141542-11:
(8*1)+(7*4)+(6*1)+(5*5)+(4*4)+(3*2)+(2*1)+(1*1)=92
92 % 10 = 2
So 141542-11-2 is a valid CAS Registry Number.
141542-11-2Relevant articles and documents
Microwave-assisted synthesis of some substituted sulfamides
Gediz Erturk, Aliye,Bekdemir, Yunus
, p. 285 - 292 (2014/01/06)
Microwave-assisted synthesis of some substituted open-chain and cyclic sulfamides, by amine-exchange reaction, was studied in a modified domestic microwave oven. Reaction times and yields under microwave radiation were compared with classical heating. Synthesis of the sulfamides under microwave irradiation gave better yields with the desired compounds, and in considerably reduced reaction times, than those obtained by classical heating. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfer, and Silicon and the Related Elements for the following free supplemental files: Additional figures.]
