
Aliphatic compounds and derivatives
Aliphatic compounds and derivatives are organic compounds characterized by straight or branched chain structures, as opposed to ring structures found in aromatic compounds. These compounds include alkanes, alkenes, alkynes, and their functionalized derivatives, playing a vital role in various chemical processes and industrial applications. At CymitQuimica, we offer a diverse selection of high-purity aliphatic compounds and their derivatives, meticulously sourced and tested to meet the stringent requirements of research and industrial needs. Our catalog covers a wide range of compounds, including hydrocarbons, alcohols, aldehydes, ketones, and acids, each known for their reactivity and versatility in organic synthesis, pharmaceuticals, and materials science. By providing top-quality aliphatic compounds and derivatives, we support researchers and professionals in achieving precise and efficient chemical transformations, fostering innovation and advancements in multiple scientific and technological fields.
Products of "Aliphatic compounds and derivatives"
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Ethyl trifluoromethanesulfonate
CAS:Formula:C3H5F3O3SPurity:97%Color and Shape:LiquidMolecular weight:178.1302Stannane, tributyl-2-propen-1-yl-
CAS:Formula:C15H32SnPurity:98%Color and Shape:LiquidMolecular weight:331.1156(2E)-1-(4-methoxyphenyl)-3-(thiophen-2-yl)prop-2-en-1-one
CAS:Purity:95.0%Molecular weight:244.30999755859375(2E)-1-(3-chlorophenyl)-3-(3-fluorophenyl)prop-2-en-1-one
CAS:Purity:95.0%Molecular weight:260.69000244140625(2E)-1-(4-methylphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
CAS:Purity:95.0%Molecular weight:312.3649902343753-allyl-6-methoxybenzo[d]thiazol-2(3H)-imine hydrobromide
CAS:Purity:95.0%Molecular weight:301.20001220703125Cyclohexane-1,2-dione
CAS:Cyclohexane-1,2-dione is a natural compound that can be found in kidney beans and other plants. It has been shown to inhibit the growth of tumor cells in vitro. Cyclohexane-1,2-dione binds to DNA polymerase, preventing replication and transcription. This reaction mechanism is similar to that of the rifamycins. Cyclohexane-1,2-dione has also been shown to bind enzymes such as nitrite ion reductase with high affinity and inhibit their activity. Cyclohexane-1,2-dione is chemically stable and does not react with metal ions or form stable complexes with biological molecules. The redox potentials for this molecule are -0.42 V (5/6) under aerobic conditions and -0.52 V (5/6) under anaerobic conditions.Formula:C6H8O2Purity:Min. 96.5%Color and Shape:PowderMolecular weight:112.13 g/mol(E)-Ethyl 3-(4-chlorophenyl)-2-cyanoacrylate
CAS:Purity:95.0%Color and Shape:Solid, No data available.Molecular weight:235.6699981689453(2E)-1-(4-ethoxyphenyl)-3-(furan-2-yl)prop-2-en-1-one
CAS:Purity:95.0%Molecular weight:242.2740020751953[2-methanesulfonyl-1-(prop-2-en-1-yl)-1H-imidazol-5-yl]methanol
CAS:Purity:95.0%Molecular weight:216.25999450683594N-Methylhydroxylamine Hydrochloride
CAS:Formula:CH6ClNOPurity:97%Color and Shape:SolidMolecular weight:83.5174(2E)-1-(2,4-dimethylphenyl)-3-(3-methylthiophen-2-yl)prop-2-en-1-one
CAS:Purity:95.0%Molecular weight:256.35998535156251-((4S,5S)-2,2-dimethyl-5-vinyl-1,3-dioxolan-4-yl)-2-(trityloxy)ethanone
CAS:Purity:98%Molecular weight:428.52801513671875