63777-54-8 Usage
Explanation
The compound is composed of 9 carbon atoms, 9 hydrogen atoms, and 3 nitrogen atoms.
Explanation
It belongs to the 1,2,3-triazole class of compounds, which are known for their diverse range of biological activities.
Explanation
The compound features a five-membered triazole ring (a ring containing three nitrogen atoms and two carbon atoms) and a methylphenylmethyl group (a phenyl group with a methyl group attached to a methylene group).
Explanation
Due to its unique structure and properties, the compound has potential applications in various fields, including the development of new drugs, agrochemicals, and materials.
Explanation
The compound serves as a valuable tool in the development of new drugs and other chemical products, as it can be used to synthesize a wide range of biologically active molecules.
Explanation
The stability of the compound is not mentioned in the provided material, so it cannot be determined.
Explanation
The solubility of the compound is not mentioned in the provided material, so it cannot be determined.
Explanation
The reactivity of the compound is not mentioned in the provided material, so it cannot be determined.
Explanation
The melting point of the compound is not mentioned in the provided material, so it cannot be determined.
Explanation
The boiling point of the compound is not mentioned in the provided material, so it cannot be determined.
Class
1,2,3-Triazole
Structure
Triazole ring and a methylphenylmethyl group
Biological Activities
Potential applications in pharmaceuticals, agrochemicals, and materials science
Synthesis
Important building block for the synthesis of various biologically active molecules
Stability
Unknown (not provided in the material)
Solubility
Unknown (not provided in the material)
Reactivity
Unknown (not provided in the material)
Melting Point
Unknown (not provided in the material)
Boiling Point
Unknown (not provided in the material)
Check Digit Verification of cas no
The CAS Registry Mumber 63777-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,7 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63777-54:
(7*6)+(6*3)+(5*7)+(4*7)+(3*7)+(2*5)+(1*4)=158
158 % 10 = 8
So 63777-54-8 is a valid CAS Registry Number.
63777-54-8Relevant academic research and scientific papers
Palladium-catalyzed oxidative C-H/C-H cross-coupling of 1-substituted 1,2,3-triazoles with furans and thiophenes
Yu, Xin,Huang, Zhendong,Liu, Wei,Shi, Suping,Kuang, Chunxiang
supporting information, p. 4459 - 4465 (2015/04/14)
Palladium-catalyzed heteroarylation of 1-substituted 1,2,3-triazoles with furans and thiophenes has been developed in the presence of pyridine and Ag2CO3. The procedure is suitable for the regioselective preparation of 1,5-disubstitu
Easy one-pot synthesis of 1-monosubstituted aliphatic 1,2,3-triazoles from aliphatic halides, sodium azide and propiolic acid by a click cycloaddition/decarboxylation process
Zhang, Zhongkui,Kuang, Chunxiang
, p. 1011 - 1014 (2013/09/02)
1-Monosubstituted aliphatic 1,2,3-triazoles were synthesized by a one-pot reaction from aliphatic halides (Cl and Br), sodium azide and propiolic acid. The yields ranged from moderate to good. The reaction was easily carried out in DMF with Cs2CO3 at 100°C by copper-catalyzed click cycloaddition/decarboxylation. The synthesis of 1-monosubstituted aliphatic 1,2,3-triazoles was achieved in a one-pot reaction from aliphatic halides (Cl, Br), sodium azide and propiolic acid with yields ranging from moderate to good. Copyright
Synthesis of substituted 1-aralkyl-1H-v-triazoles
-
, (2008/06/13)
Substituted 1-aralkyl-1H-v-triazoles are prepared from a suitable 1-aralkyl-1H-v-triazole by a process comprising an alkylation step and dependent on the product desired suitably followed by an oxidation step and decarboxylation step.
