Ketones

Please enquire for more information about 2-((4-Methoxyphenyl)methylene)indan-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-((4-(4,5-Dichloroimidazolyl)phenyl)amino)-5,5-dimethylcyclohex-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-(phenylmethylthio)-3-hydroquinazolin-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-phenyl-2-((phenylamino)methylene)cyclohexane-1,3-dione is an acid hydrazide compound that has various applications. It is derived from Streptomyces and possesses unique properties that make it useful in different fields. This compound has been studied for its potential as a therapeutic agent for various conditions, including neurological disorders and cancer.

Please enquire for more information about 3-((4-(Trifluoromethoxy)phenyl)amino)cyclohex-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Ethyl-4-hydroxy-2-methyl-3(2H)-furanone is a colorless liquid that has a fruity, sweet odor. It is used in the manufacture of flavors and fragrances. 5-Ethyl-4-hydroxy-2-methyl-3(2H)-furanone can be obtained by the reaction of butanedione with dilute sulfuric acid, followed by treatment with an absorber containing propylene glycol and 4-ethyl-2methoxyphenol. The product is then treated with radiation energy to produce furfural, which reacts with anthranilate to form methyl anthranilate. Methyl anthranilate can be converted into phenylmethyl by reacting it with glycosidase.

Please enquire for more information about 5-(2-methylpropyl)-2-(((4-(1,2,4-triazolyl)phenyl)amino)methylene)cyclohexane-1,3-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 6,7-dimethoxy-2-(4-methylphenyl)benzo[d]1,3-oxazin-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-((4-Acetylphenyl)amino)-2-chloro-5-methylcyclohex-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-((4-Chlorophenyl)sulfonyl)-4-ethoxybut-3-en-2-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-iodo-3-(benzylamino)cyclohex-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Benzoyl-1,3-indanedione is a hydrogen bond donor that has been used as a nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation. 2-Benzoyl-1,3-indanedione is a molecule that reacts with amines to form reaction products. It has antimicrobial activity due to its ability to bind to DNA and inhibit protein synthesis in bacteria. The binding of 2-benzoyl-1,3-indanedione to DNA occurs via the nitrogen nucleophile on its benzene ring attacking the base of an adenine or guanine base pair. This leads to the formation of an amide bond between the indane group and one of the bases. The primary amine group on this molecule can also react with other amines to form secondary amides. This process can be carried out at low concentrations by dilution method.

Applications (Z)-1-(Benzo[b]​thiophen-​2-​yl)ethanone Oxime is an isomer of N-​(1-​Benzo[b]​thiophen-​2-​yl-​ethyl)​-​hydroxylamine a reagent used in the preparation of Zileuton, an anti-asthmatic drug.
References Guinchard, X. et al.: J. Org. Chem., 73, 2028 (2008)

Applications 5-(Trifluoromethyl)-1-indanone (cas# 150969-56-5) is a useful research chemical.

Applications 1-(2-Hydroxy-4,6-dimethylphenyl)-ethanone was investigated for its properties as an antibacterial agent and urease inhibitory effects.
References Ngan, L.T., et al.: J. Agri. Chem., 60, 9062 (2012); Chermenskaya, T.D., et al.: Industrial. Crops. Prod., 36, 122 (2012);

Stability Volatile
Applications Cyclobutanone is a member of cycloketone compounds that have potential genotoxic and cytotoxic effects and are most commonly found in irradiated food.
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 Anandon, A., et al.: EFSA Journal, 9, 1930 (2011); Delincee, H., et al.: Radiat. Phys. Chem., 63, 431 (2002); Obana, H. ,et al.: J. Health Sci., 52, 375 (2006)

Applications 5,6-Dihydroimidazo[4,5,1-jk][1]benzazepine-2,7(1H,4H)-dione (cas# 92260-81-6) is a compound useful in organic synthesis.

Applications 4'-Hydroxyflavanone (cas# 6515-37-3) could be a useful antitumor agent, specifically studied as a strong aromatase inhibitor against estrogen-dependent breast cancer.
References Kizilcan, D. S., et al.: Struct. Chem., 31, 1339 (2020)

Applications 3,​3-​Dimethyl-​2,​4-​pentanedione is used in asymmetric hydrosilation of ketones.
References Kuwano, R., et al.: Bull. Chem. Soc. Jpn., 73, 485 (2000).

Applications 5-Acetoxy-3-chloro-2-pentanone (cas# 13051-49-5) is a compound useful in organic synthesis.

Impurity: Propafenone EP Impurity H
Applications: Flavanone (Propafenone EP Impurity H) is a Propafenone (P757500) impurity.
References Kitagawa, S., et al.: Biol. Pharm. Bull., 29, 1 (2006), Boccard, J., et al.: Eur. J. Pharm. Sci., 36, 254 (2009),

Applications 4-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-2-butanone is a useful synthetic intermediate. It is a reagent used to prepare moverastin derivatives, an inhibitor of tumor cell migration. It can also be used in preparation of substituted alkene derivatives capable of releasing fragrant compounds.
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 Sawada, M., et al.: Bioorg. Med. Chem. Lett., 21, 1385 (2011);