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1H-Pyrazole, 1-methyl-4-phenyl-3-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96256-50-7

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96256-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96256-50-7 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, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96256-50:
(7*9)+(6*6)+(5*2)+(4*5)+(3*6)+(2*5)+(1*0)=157
157 % 10 = 7
So 96256-50-7 is a valid CAS Registry Number.

96256-50-7Downstream Products

96256-50-7Relevant academic research and scientific papers

Intermolecular Palladium(0)-Catalyzed Atropo-enantioselective C-H Arylation of Heteroarenes

Baudoin, Olivier,Cramer, Nicolai,Guo, Shu-Min,Nguyen, Qui-Hien,Royal, Titouan

supporting information, p. 2161 - 2167 (2020/03/03)

Atropisomeric (hetero)biaryls are motifs with increasing significance in ligands, natural products, and biologically active molecules. The straightforward construction of the stereogenic axis by efficient C-H functionalization methods is extremely rare an

Synthesis of trifluoromethylated pyrazoles from trifluoromethylenaminones and monosubstituted hydrazines

Touzot, Aline,Soufyane, Mustapha,Berber, Hatice,Toupet, Lo?c,Mirand, Catherine

, p. 1299 - 1304 (2007/10/03)

Cyclocondensation of monosubstituted hydrazines 2a-c with trifluoromethylenaminones 1a-c afforded 3-CF3 and (or) 5-CF3 pyrazoles 3-6. Addition of N-methylhydrazine to enaminone led to 3-CF3 pyrazole as the major product, w

4-Substituted 5-Amino-1-methyl-3-trifluoromethylpyrazoles: Structural Determination by Means of Carbon-13 Nuclear Magnetic Resonance Spectrometry

Nishiwaki, Tarozaemon,Arakawa, Hiroki,Kikukawa, Hirofumi

, p. 198 - 199 (2007/10/03)

Regioselective formation of 5-amino-4-aryl-1-methyl-3-trifluoromethylpyrazoles from 3-oxo-2-aryl-4,4,4-trifluorobutanenitrile and methylhydrazine was confirmed by 13C NMR spectrometry.

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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