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1H-1,2,3-Triazole, 4-(4-methoxyphenyl)-1-phenyl-5-(trifluoromethyl)- is a complex organic compound belonging to the triazole family. It is characterized by a triazole ring, which is a five-membered ring containing three nitrogen atoms and two carbon atoms. In this specific compound, the triazole ring is substituted with a 4-methoxyphenyl group at position 4, a phenyl group at position 1, and a trifluoromethyl group at position 5. This molecule is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique structure and properties. The presence of the methoxy group provides additional functionality, while the trifluoromethyl group imparts lipophilicity and stability to the molecule.

96256-62-1

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96256-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96256-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,5 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 96256-62:
(7*9)+(6*6)+(5*2)+(4*5)+(3*6)+(2*6)+(1*2)=161
161 % 10 = 1
So 96256-62-1 is a valid CAS Registry Number.

96256-62-1Downstream Products

96256-62-1Relevant academic research and scientific papers

Aryl trifluoromethyl-1,2,3-triazoles

Meazza, G.,Zanardi, G.

, p. 199 - 206 (2007/10/02)

Diaryl-substituted trifluoromethyl-1,2,3-triazoles have been synthesised from aromatic azides and various substituted 1-aryl-3,3,3-trifluoro-1-propynes.The spectroscopic characteristics of the products and the regioselectivity of the reaction are discusse

Studies on Organic Fluorine Compounds. XLII. Synthesis and Reactions of Phenyltrifluoromethylacetylenes

Kobayashi, Yoshiro,Yamashita, Toshinori,Takahashi, Katsuhiro,Kuroda, Hisashi,Kumadaki, Itsumaro

, p. 4402 - 4409 (2007/10/02)

Phenyltrifluoromethylacetylene (4a) was synthesized by the pyrolysis of triphenylphosphonium α-(trifluoroacetyl)benzylide (3a), which was easily derived from benzyl halide (1a).This method can be used for the synthesis of 4-substituted-phenyltrifluoromethylacetylenes (4).The 1,3-dipolar reaction of 4 with diazomethane and phenyl azide proceeds readily to give trifluoromethylated pyrazoles and triazoles.Keywords - trifluoromethyl; acetylene; 1,3-dipolar reaction; intramolecular Wittig reaction; trifluoroacetylphosphonium ylide; pyrazole; diazomethane; phenyl azide

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