Carboxylic Acids

Applications Methylboronic Acid is a methylated derivative of boronic acid, a building block towards various intermediates in suzuki coupling.
References Baker, J. O., et al.: Biochem.. 22, 2098 (1983); Garner, C.W., et al.: J. Biol. Chem., 255, 5064 (1980)

Applications Z-2-Fluoro-3-(3-pyridyl)acrylic Acid (cas# 359435-42-0) is a compound useful in organic synthesis.

Applications 3-Furoic Acid, is metabolized by Corynebacterium fascians from soil, limonoid metabolism based on a biological studies.
References Hasegawa, S., et al.: J. Arg. Food Chem., 31, 807 (1983)

Applications 3-(2,3-Dihydroxyphenyl)propionic acid is a degradation product of the aromatic compound Phenylpropionate (PP).
References Provencher, S., et al.: Biochemistry, 20, 33 (1981), Ferrandez, A., et al.: J. Bacteriol., 179, 2573 (1997), Torres, B., et al.: J. Biol. Chem., 278, 27575 (2003),

Applications 5-Chloronicotinic Acid is used as reagent/reactant luminescence and hydrothermal preparation of cobalt/cadmium/lead chloronicotinate phenanthroline MOF.
References Gao, Z.Q., et al.: J. Solid State Chem., 241, 121-130 (2016)

Applications 4-Isopropylphenylacetic acid (cas# 4476-28-2) is a useful research chemical.

Applications 3-Hydroxyhomophthalic acid (cas# 42421-12-5) is a useful research chemical.

Applications 2-(bis(2-(tert-butoxy)-2-oxoethyl)amino)acetic acid (cas# 171557-31-6) is a useful research chemical.

Stability Hygroscopic
Applications 3-Sulfanylhexyl Acetate is a precursor of 3-mercaptohexan-1-ol (M225270) found in grape juice.
References Harsch, M.J., et al.: J. Agri. Food. Chem., 61, 3703 (2013); Makhotkina, O., et al.: Food. Chem., 135, 486 (2012);

Applications 5-Ethyl-6-hydroxyhexanoic Acid is an intermediate in the synthesis of metabolites of Bis(2-ethylhexyl) Phthalate (DEHP) (B433850).
References Kaulen, J., et al.: Tetrahedron., 38, 3299 (1982);

Applications 2-Cyclohexylideneacetic acid (cas# 1552-91-6) is a useful research chemical.

Applications 2,2-Dimethylbutyrate (DMB) is a potential treatment for thalassemia and hemoglobinopathies.
References Yeh, K., et al.: J. Pharmacokinet. Biopharm., 6, 79 (1978), Cunningham, M., et al.: Blood, 104, 34 (2004), Rund, D., et al.: N. Engl. J. Med., 353, 1135 (2005),

Applications 5-(Benzyloxy)-2-Hydroxybenzoic Acid (cas# 16094-44-3) is a useful research chemical.

Applications 1,4-Cubanedicarboxylic acid

Impurity Ketoprofen EP Impurity G
Applications 3-​(2-Hydroxyethyl)​benzoic Acid (Ketoprofen EP Impurity G) is an impurity in the synthesis of Ketoprofen (K200800), anti-inflammatory (1,2); analgesic.
References 1. Ueno, K. et al.: J Med Chem. 1976 Jul;19(7):941-6. 2. Jamali, F. et al.: Clin Pharmacokinet. 1990 Sep;19(3):197-217.

Stability Hygroscopic
Applications Magnesium acetate tetrahydrate (cas# 16674-78-5) is a useful research chemical.

Applications 5-Hydroxy-3-phenylbenzoic Acid can be used in biological study of preparation and identification of hydroxybenzoic acids as lactate receptor agonists and antilipolytics. It can also be used in discovery of new series of BRD4(1) inhibitors using protein-ligand docking and structure-guided design.
References Duffy, B. C., et al.: Bioorg Med Chem Lett, 25, 2818 (2015), Dvorak, C. A., et al.: ACS Med Chem Lett, 3, 637 (2012)

Applications 2,5-Dimethylthiophene-3-boronic acid

[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]acetic acid is a potent antimicrobial agent that inhibits the growth of bacteria by binding to the 50S ribosomal subunit. It has shown antiinflammatory properties in animal models of bowel disease, skin cancer, and autoimmune diseases. This drug has also been shown to have no observable toxicity in humans at doses up to 5000 mg/day for 28 days. The drug binds to a number of enzymes including reactive oxygen species (ROS) scavengers and metabolic enzymes. There are no known drug interactions with this drug and it can be used safely with other nonsteroidal antiinflammatory drugs (NSAIDs).

Please enquire for more information about 5-(5-Chloro-1-methyl-1H-benzimidazol-2-yl)pentanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Triflic acid is a strong acid that reacts with nucleophiles such as water, alcohols, and amines. It is used in organic synthesis for desulfurization reactions, for example to convert thiophene to benzothiophene. Triflic acid is a synthetic chemical that is prepared by the reaction of sulfur trioxide with chlorotrifluoroethanesulfonyl fluoride. The protonation of the triflic acid molecule generates a sulfide anion. This anion then reacts with a nucleophile (e.g., chloride ion) to generate a chloride anion and regenerate the triflic acid molecule, which can then react again with another nucleophile. The reaction mechanism is shown below: HSOClF + NH3 → HSOClF + NH2Cl HSOClF + Cl- → HSO-Cl- + Cl The reaction mechanism for this process is shown below: HSOCl

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