
Hydrocarbon Building Blocks
Hydrocarbon building blocks are organic compounds consisting solely of carbon and hydrogen atoms. These fundamental structures serve as the basis for synthesizing a wide variety of complex molecules. Hydrocarbon building blocks are used in the development of pharmaceuticals, polymers, and other organic compounds. At CymitQuimica, we offer a broad range of high-quality hydrocarbon building blocks to facilitate your synthetic and research projects.
Subcategories of "Hydrocarbon Building Blocks"
Found 5575 products of "Hydrocarbon Building Blocks"
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2-((4-Methoxyphenyl)ethynyl)aniline
CAS:Formula:C15H13NOPurity:97.0%Color and Shape:SolidMolecular weight:223.275[S(R)]-N-[(1S)-1-(2′,6′-Diisopropyl)-(1,1′-biphenyl)-2-yl]-2-(diphenylphosphino)ethyl]-2-methyl-2-propanesulfinamide
CAS:Purity:95%Molecular weight:569.79[4-(2-propyn-1-yloxy)phenyl]amine hydrochloride
CAS:Formula:C9H10ClNOPurity:95.0%Molecular weight:183.647-Octyn-1-ol
CAS:Controlled Product<p>Applications 7-Octyn-1-ol is used in the synthesis of the sex pheromone of the citrus leafminer, Phyllocnistis citrella.<br>References Ando, T., et al.: Agric. Biol. Chem., 49, 3633 (1985), Beevor, P., et al.: J. Chem. Ecol., 12, 1 (1986), Kerr, D., et al.: J. Med. Chem., 33, 1958 (1990), McElfresh, J., et al.: Ecology, 82, 3505 (2002),<br></p>Formula:C8H14OColor and Shape:NeatMolecular weight:126.20Vinylcyclopropane
CAS:Controlled Product<p>Stability Highly Volatile<br>Applications Vinylcyclopropane is a useful synthetic intermediate. Vinylcyclopropane and its derivatives can participate in a variety of transition-metal-catalyzed multicomponent cycloadditions to produce five- to eight-membered carbocycles.<br>References Jiao, L., et al.: J. Org. Chem., 78, 6842 (2013); Pasto, D., et al.: Tetrahedron Lett., 9, 713 (1979); Larock, R., et al.: Tetrahedron, 52, 2743 (1996)<br></p>Formula:C5H8Color and Shape:NeatMolecular weight:68.12Triisopropylsilyl trifluoromethanesulphonate
CAS:<p>Triisopropylsilyl trifluoromethanesulphonate (TIPS) is a naturally occurring compound that inhibits the enzyme dipeptidyl peptidase IV (DPP-IV). It has been shown to be active against alopecia areata in a mouse model and may have therapeutic potential for other autoimmune diseases. TIPS also has an inhibitory effect on sodium-dependent glucose transport, which may be useful in the treatment of hypertension. The reactive group of TIPS is hydroxyl, which can form a covalent bond with serine proteases and inhibit their activity. This reaction mechanism provides a new way to treat disorders such as metabolic diseases and infectious diseases. TIPS also has an inhibitory effect on ns3 protease, which is involved in the replication of human immunodeficiency virus type 1 (HIV-1) and other retroviruses.</p>Formula:C10H21F3O3SSiPurity:Min. 95%Color and Shape:Colourless Clear LiquidMolecular weight:306.42 g/mol1-Amino-1-cyclopentanecarboxamide
CAS:<p>1-Amino-1-cyclopentanecarboxamide is a bicyclic heterocycle that has been shown to have therapeutic effects in the treatment of autoimmune diseases and cancer. It is structurally related to chemokines, which are cytokines that induce inflammatory responses by activating the immune system. 1-Amino-1-cyclopentanecarboxamide binds to specific receptors on white blood cells, resulting in an increase in the production of chemokines and other proinflammatory molecules. This leads to an increase in inflammation, as well as an increase in blood pressure. The chemical also has anti-inflammatory properties and can be used for the treatment of inflammatory diseases such as arthritis. 1-Amino-1-cyclopentanecarboxamide has been shown to inhibit cancer cell growth by inducing apoptosis (programmed cell death).</p>Formula:C6H12N2OPurity:Min. 95%Color and Shape:PowderMolecular weight:128.17 g/mol2-Nitropropane
CAS:<p>2-Nitropropane is a pharmacological agent that is used for the treatment of bacterial infections. It is a nitroalkane, which are compounds with nitro groups in their molecular structure. 2-Nitropropane has been shown to inhibit DNA synthesis by binding to nuclear dna and inhibiting enzyme activities in vitro. Toxicological studies on 2-nitropropane have been conducted and show that it does not cause any adverse effects at low doses. The mechanism of action for 2-nitropropane has been investigated and found to inhibit the enzyme activity of nitrate reductase, which leads to an accumulation of the toxic nitrite ion (NO2-) in cells.</p>Formula:C3H7NO2Purity:Min. 95%Color and Shape:Colorless PowderMolecular weight:89.09 g/molHydroxypropanedial
CAS:<p>Hydroxypropanedial is a hydroxy group-containing compound that is not found in natural sources. It has antioxidative properties, which may be due to its ability to scavenge reactive oxygen species or donate hydrogen atoms to free radicals. The compound also has cyclohexane ring and carbonyl groups, which are responsible for the hydroxyl and carboxylic acid functionalities respectively. This substance is used as a chromatographic reagent to measure second-order rate constants of reactions involving hydroxyl radicals. Hydroxypropanedial absorbs light strongly at wavelengths shorter than 300 nm, which is the most effective wavelength range for uv absorption in biological systems.</p>Formula:C3H4O3Purity:Min. 95%Color and Shape:Off-White To Light (Or Pale) Brown SolidMolecular weight:88.06 g/molHexabromoethane
CAS:<p>Hexabromoethane is a metal chelate that has been shown to activate the polymerization of cyclohexane rings. It is often used as a light-sensitive initiator for the production of polymers, such as polyethylene. Hexabromoethane can also be found in some halogenated compounds and hydroxyl groups. The molecule is made up of six bromine atoms, an ethane chain, and one hydrogen atom. Hexabromoethane has significant interactions with other functional groups, including hydroxyls and monomers.</p>Formula:C2Br6Purity:Min. 95%Color and Shape:PowderMolecular weight:503.45 g/molBis[(pinacolato)boryl]methane
CAS:<p>Bis[(pinacolato)boryl]methane is a bifunctional organoboron reagent with an allyl group on one end and a cyclopropane on the other end. It is useful in organic synthesis as a nucleophile for allylation, as well as for the synthesis of unsymmetrical cyclopropanes. This compound can be used to catalyze asymmetric methods, such as the synthesis of alicyclic compounds. Bis[(pinacolato)boryl]methane can also be used to synthesize biomolecules.</p>Formula:C13H26B2O4Purity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:267.97 g/molEthanesulfonic acid, 70% aqueous solution
CAS:<p>Ethanesulfonic acid solution - 70 wt. % in H2O is a monosodium salt that is used as an enzymatic reagent for the determination of bacteria and fungi, as well as for the detection of infectious diseases. It has been shown to be effective against microdialysis probes with a high degree of sensitivity and specificity. Ethanesulfonic acid solution - 70 wt. % in H2O has been shown to have significant physiological effects on various regions of the body, including bowel disease, polymerase chain reaction (PCR), glycol ethers, antimicrobial agents, and radiation. Ethanesulfonic acid solution - 70 wt. % in H2O also inhibits the growth of bacteria by acting as a coumarin derivative that reacts with nucleotides to form dinucleotide phosphate, which blocks DNA synthesis and transcription from RNA templates.</p>Formula:C2H6O3SPurity:(Titration) 68.0 To 72.0%Color and Shape:Clear LiquidMolecular weight:110.13 g/molPerfluoroheptanoyl chloride
CAS:<p>Perfluoroheptanoyl chloride is a fluorinated hydrocarbon that is used as a surfactant in detergent compositions. It has been shown to be biostable, which means it does not react with other molecules in the environment. This compound also has low environmental toxicity because of its resistance to peroxidation and its ability to form stable complexes with metals. Perfluoroheptanoyl chloride has been shown to cause allergic reactions in some people and may cause adverse effects on animal health. Research on the effects of perfluoroheptanoyl chloride on Xenopus oocytes has demonstrated that this compound can affect gene expression and result in cell death.</p>Formula:C7CIF13OPurity:Min. 95%Color and Shape:Colourless LiquidMolecular weight:382.51 g/mol2,2,4,4,6,8,8-Heptamethylnonane
CAS:<p>2,2,4,4,6,8,8-Heptamethylnonane is a hydrogenated form of 2-methylnonane. It is used as a model system for fatty acids in order to study the kinetics of air entrainment and constant pressure distillation. The chemical stability of 2,2,4,4,6,8,8-heptamethylnonane has been shown to be excellent when heated at 200°C under nitrogen. This compound can also be used as an analytical method for ethylene diamine in pharmaceutical preparations of sodium salts and boron nitride. The use of 2-methylnonane as a starting material may lead to the production of chinese herb by reacting with acetic acid or formic acid.</p>Formula:C16H34Purity:Min. 95%Color and Shape:PowderMolecular weight:226.44 g/mol


