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4-(trifluoromethyl)-1-cyclohexene is an organic compound with the molecular formula C7H9F3. It is a colorless liquid at room temperature and has a molecular weight of 162.14 g/mol. This chemical is characterized by a cyclohexene ring, which is a six-membered carbon ring with one double bond, and a trifluoromethyl group (-CF3) attached to the fourth carbon atom. The trifluoromethyl group imparts unique properties to the molecule, such as increased lipophilicity and stability. 4-(trifluoromethyl)-1-cyclohexene is synthesized through various chemical reactions and is used as an intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is essential to handle 4-(trifluoromethyl)-1-cyclohexene with proper safety measures and in a controlled environment.

349-51-9

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349-51-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349-51-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 349-51:
(5*3)+(4*4)+(3*9)+(2*5)+(1*1)=69
69 % 10 = 9
So 349-51-9 is a valid CAS Registry Number.

349-51-9Downstream Products

349-51-9Relevant academic research and scientific papers

Synthesis, Characterization, Cytotoxicity, and Time-Dependent NMR Spectroscopic Studies of (SP-4-3)-Oxalato[(1R,2R,4R/1S,2S,4S)-(4-trifluoromethyl-cyclohexane-1,2-diamine)]platinum(II)

Hizal, Selin,Hejl, Michaela,Jungmann, Christoph,Jakupec, Michael A.,Galanski, Markus,Keppler, Bernhard K.

, p. 856 - 864 (2019)

The oxaliplatin derivative (SP-4-3)-oxalato[(1R,2R,4R/1S,2S,4S)-(4-trifluoromethyl-cyclohexane-1,2-diamine)]platinum(II) hosting a trifluoromethyl group at position 4 of the cyclohexane ring is presented. The ligand was synthesized as an 1R,2R,4R/1S,2S,4S racemic mixture starting from 4-trifluoromethyl-cyclohexanol over five steps and coordinated to platinum to yield first the dichlorido and subsequently the oxalato complex. This novel compound and its analogue featuring a (13C2)oxalate ligand were characterized by multinuclear (1H, 13C, 15N, 19F, 195Pt) one- and two-dimensional NMR spectroscopy. Ligand exchange and adduct formation reactions with DMSO, NaCl, CaCl2, l-methionine, and 5′-GMP were investigated via time-dependent measurements by 19F and 13C NMR spectroscopy. The cytotoxicity of the title complex was investigated in three human cancer cell lines; the IC50 values were found in the low micromolar range, attesting moderate to high antiproliferative activity, depending on the cell line.

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