
Heterocycles with Sulphur (S)
Subcategories of "Heterocycles with Sulphur (S) "
Found 1000 products of "Heterocycles with Sulphur (S) "
Thiophene
CAS:Controlled ProductApplications Thiophene is used as a building block of various organic molecules and pharmaceuticals providing functional properties.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Prasad, B. et al.: Chem. Comm., 48, 10434 (2012); Freitas, V. et al.: Struct. Chem., 24, 661 (2013);Formula:C4H4SColor and Shape:ColourlessMolecular weight:84.142-Benzoyl-5-ethylthiophene
CAS:Controlled ProductFormula:C13H12OSColor and Shape:NeatMolecular weight:216.299Benzo[b]thiophen-2(3H)-one
CAS:Controlled ProductApplications Benzo[b]thiophen-2(3H)-one is a reactant used in the synthesis of merocyanines dyes.
References Glauert, R. & Mann, F.: J. Chem. Soc., 5012 (1952)Formula:C8H6OSColor and Shape:NeatMolecular weight:150.24-Chlorothiophenol(4-Chlorobenzenethiol)
CAS:Controlled ProductApplications 4-Chlorobenzenethiol is a reagent used in the synthesis of small-molecule inhibitors of the protein geranylgeranyltransferase Type I (GGTase-I), acting as anti-tumor agents. Also is used in the synthesis of β-sulfanyl carbonyl compounds via Michael addition.
References Ranu, B. et al.: Tetrahedron, 60, 4183 (2004); J. Med. Chem., 43, 2310 (2000);Formula:C6H5ClSColor and Shape:NeatMolecular weight:144.62Dibenzothiophene
CAS:Applications Dibenzothiophene is commonly used in microbial studies as a sole, organic sulfur and carbon source for growth. Research concerning the biodegradation of dibenzothiophene by different types of bacteria is a currently being carried out, as these bacteria have the ability to breakdown other harmful polycyclic hydrocarbons (PAH) as well. This may prove to be a very practical method in removing PAH’s from soils, sludge and crude oils.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Bastiaens, L., et al.: Appl. Environ. Microb., 66, 1834 (2000); Gunam, I., et al.: J. Microbiol. Biotechn., 23, 473 (2013); Omori, T., et al.: Appl. Environ. Microb., 58, 911 (1992)Formula:C12H8SColor and Shape:NeatMolecular weight:184.26N-(4-Chlorobenzyl)-1-(5-nitrothiophen-2-yl)methanamine
CAS:Controlled ProductApplications N-(4-Chlorobenzyl)-1-(5-nitrothiophen-2-yl)methanamine is an analogue of GSK 4112 (G797700) which is a synthetic ligand for REV-ERBα, a member of the nuclear receptor superfamily that functions as a receptor for the porphoryin heme. GSK 4112 mimics the action of heme acting as agonist and suppresses the expression of REV-ERBα target genes involved in gluconeogenesis.
References Kojetin, D. et al.: ACS Chem. Biol., 6, 131 (2011); Grant, D. et al.: ACS Chem. Biol., 5, 925 (2010)Formula:C12H11ClN2O2SColor and Shape:NeatMolecular weight:282.752-Thiopheneethanol Tosylate
CAS:Controlled ProductApplications Intermediate in the preparation of Rotigotine
References Janssens, F., et al.: J. Med. Chem., 29, 2290 (1986),Formula:C13H14O3S2Color and Shape:NeatMolecular weight:282.38[2-(Thiophene-2-yl)ethyl]amine
CAS:Controlled ProductFormula:C6H9NSColor and Shape:NeatMolecular weight:127.2075-(2-Sulfanylidene-3H-1,3-thiazol-4-yl)thiophene-2-carboxamide
CAS:Controlled ProductApplications 5-(2-Sulfanylidene-3H-1,3-thiazol-4-yl)thiophene-2-carboxamide is a compound involved in the multi-step synthesis of arotinolol hydrochloride.
References Liu, H., et al.: Zhongguo Yiyao Gongye Zazhi, 42, 641-644 (2011)Formula:C8H6N2OS3Color and Shape:NeatMolecular weight:242.342,4,7-Trimethyldibenzothiophene
CAS:Controlled ProductApplications 2,4,7-Trimethyldibenzothiophene is found in crude oil and can be used to determine the maturity of the oil.
References Hegazi, A.H., et. al.: Polycycl. Aromat. Comp., 24, 123 (2004)Formula:C15H14SColor and Shape:NeatMolecular weight:226.343-Acetyl-2,5-dimethylthiophene
CAS:Controlled ProductApplications 3-Acetyl-2,5-dimethylthiophene Standard (cas# 2530-10-1) is a useful research chemical.
Formula:C8H10OSColor and Shape:NeatMolecular weight:154.23Benzo[b]thiophene
CAS:Applications Benzo[b]thiophene has application in organic as well as pharmaceutical industry as a component in the synthesis of Raloxifene, a breast cancer therapeutic, or hydrodesulfurization reactions.
References Buccella, D. et al.: J. Am. Chem. Soc., 130, 16187 (2008); Gennari, L. et al.: Exp. Opin. Drug Saftey, 7, 259 (2008);Formula:C8H6SColor and Shape:WhiteMolecular weight:134.2Thiophene-2-amidine hydrochloride
CAS:2-Amidinothiophene Hydrochloride is a drug that is used as an anti-inflammatory agent. It is an isoform of amidinothiophene, which inhibits the production and release of cyclic nucleotides. 2-Amidinothiophene Hydrochloride has shown activity against tracheal muscle, adenosine receptors, and phosphodiesterase isoenzymes. This drug binds to the ATP binding site of the enzyme cyclic nucleotide phosphodiesterase, blocking the breakdown of cAMP into AMP and then ADP.
Formula:C5H7ClN2SPurity:Min. 95%Molecular weight:162.64 g/molMethyl 3-(((phenylcarbonylamino)thioxomethyl)amino)thiophene-2-carboxylate
CAS:Please enquire for more information about Methyl 3-(((phenylcarbonylamino)thioxomethyl)amino)thiophene-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C14H12N2O3S2Purity:Min. 95%Color and Shape:PowderMolecular weight:320.39 g/mol4-Hydroxythiophenol
CAS:4-Hydroxythiophenol is an organic compound with the molecular formula C6H4OHO. It is a white crystalline solid that is soluble in water and ethanol. 4-Hydroxythiophenol has been shown to inhibit the growth of bacteria by reacting with free intracellular hydroxyl groups, which are necessary for the biosynthesis of cell walls. This molecule also reacts with other biological molecules, such as nucleic acids and proteins, to form covalent bonds. 4-Hydroxythiophenol has been shown to be effective against both Gram-positive and Gram-negative bacteria in vitro assays.Formula:C6H6OSPurity:(%) Min. 75%Color and Shape:PowderMolecular weight:126.18 g/mol2-Amino-4-methylthiophene-3-carboxamide
CAS:2-Amino-4-methylthiophene-3-carboxamide is a small molecule that is a potent inhibitor of the JAK2 kinase. This enzyme is associated with human fibrosis and has been shown to be involved in the development of liver fibrosis in rats. 2-Amino-4-methylthiophene-3-carboxamide inhibits the production of cytokines such as IL1α, IL6, and TNFα. It also blocks the activation of transcription factors such as NFκB, which are involved in inflammation. The compound has been shown to be orally active and has demonstrated efficacy in animal studies. Analogues have also been synthesized for this compound that show similar activity.Formula:C6H8N2OSPurity:(%) Min. 85%Color and Shape:PowderMolecular weight:156.21 g/mol4-Methylthiophenol
CAS:4-Methylthiophenol is a colorless liquid that is soluble in water. It has a molecular weight of 98.12 and an empirical formula of C6H7O2S. 4-Methylthiophenol is used as an analytical reagent, solvent, and chemical intermediate. It exhibits hydrogen bonding interactions with sodium carbonate and trifluoroacetic acid and forms a salt with sodium carbonate. The molecule's stability increases when it interacts with amines and the presence of nucleophiles such as water or alcohols. 4-Methylthiophenol has been shown to be effective at enhancing the fluorescence signal emitted by amines, which makes it useful for laser ablation mass spectrometry (LA-MS). 4-Methylthiophenol can also be used for kinetic energy measurements using FTIR spectroscopy because it will absorb infrared light at 1680 cm−1 from the CO2 laser beam.Formula:C7H8SPurity:Min. 95%Color and Shape:White PowderMolecular weight:124.2 g/mol2,5-Diphenylthiophene
CAS:2,5-Diphenylthiophene is a fluorescent dye that has been used to study the transport properties of aromatic molecules. This compound is characterized by two phenyl groups and a thiophene ring with a sulfur atom in the 2 position. The red shift observed for this compound is due to the electron withdrawing effect of the sulfur atom. 2,5-Diphenylthiophene has shown inhibition activity against Nepeta cataria, which may be due to its ability to form sulfoxide bonds with proteins. It has also been found that this molecule can polymerize and form polymers in solution. This property is related to its morphology, which is irregular and rod-like in shape.Formula:C16H12SPurity:Min. 95%Molecular weight:236.33 g/mol5-(2-Chlorophenyl)thiophene-2-carboxylic acid
CAS:5-(2-Chlorophenyl)thiophene-2-carboxylic acid is a reagent, complex compound, and useful intermediate that belongs to the class of fine chemicals. CAS No. 500604-91-1 is a speciality chemical that is used as a versatile building block in research chemicals and as a reaction component for the synthesis of new drugs. It is also an excellent building block for synthesizing 1,4-benzothiazepines and other heterocyclic compounds.
Formula:C11H7ClO2SPurity:Min. 95%Color and Shape:PowderMolecular weight:238.69 g/mol4-Ethyl-5-methylthiophene-3-carboxylic acid
CAS:4-Ethyl-5-methylthiophene-3-carboxylic acid is a chemical compound that can be used as an intermediate for the synthesis of other compounds. It is also a building block and a versatile building block in organic synthesis, with many applications in research and industry. This compound has a CAS number of 884497-34-1 and is classified as a speciality chemical.Formula:C8H10O2SPurity:Min. 95%Color and Shape:PowderMolecular weight:170.23 g/mol

