
Carboxylic Acids
Carboxylic acids are organic molecules characterized by having a carboxyl-type functional group (-COOH). These acids are fundamental in various chemical reactions, including esterification, amidation, and decarboxylation. Carboxylic acids are widely used in the production of pharmaceuticals, polymers, and agrochemicals. In this section, you can find a large number of carboxylic acids ready to be used. At CymitQuimica, we provide a broad range of high-quality carboxylic acids to support your research and industrial applications.
Found 12454 products of "Carboxylic Acids"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
14-Pentadecynoic Acid
CAS:Controlled ProductFormula:C15H26O2Color and Shape:NeatMolecular weight:238.3664-(tert-Butoxy)phenylboronic Acid
CAS:Controlled Product<p>Applications 4-tert-Butoxyphenylboronic Acid is a compound used in the preparation of nitrophenylphenol via cross-coupling reaction of nitrohalobenzenes with phenylboronic acids and deprotection.<br>References Kumamoto, N., et al.: Preparation of nitrophenylphenol, JP 2001055360 (2001);<br></p>Formula:C10H15BO3Color and Shape:NeatMolecular weight:194.042-Mercaptobenzoic Acid Hydrazide
CAS:Controlled ProductFormula:C7H8N2OSColor and Shape:NeatMolecular weight:168.216B-(4-[1,1'-biphenyl]-4-yl-6-phenyl-1,3,5-triazin-2-yl)-Boronic acid
CAS:Controlled ProductFormula:C21H16BN3O2Color and Shape:NeatMolecular weight:353.182Difluoro(trimethylsilyl)methylphosphonic Acid
CAS:Controlled ProductFormula:C4H11F2O3PSiColor and Shape:NeatMolecular weight:204.184trans-4,4-Dimethylpent-2-enoic Acid
CAS:Controlled ProductFormula:C7H12O2Color and Shape:NeatMolecular weight:128.1693,4-Bis(isobutoxycarbonyl)benzoic Acid
Controlled Product<p>Applications 3,4-Bis(isobutoxycarbonyl)benzoic Acid is a useful reagent in organic synthesis.<br></p>Formula:C17H22O6Color and Shape:NeatMolecular weight:322.353Vinylacetic Acid
CAS:Controlled Product<p>Stability Light Sensitive<br>Applications Vinylacetic Acid can be used as a reagent in the synthesis of 4-Phenyl-3-butenoic Acid which is an in vivo inhibitor of the peptide amidating enzyme peptidylglycine hydroxylase.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Bradbury, A.F., et al.: Eur. J. Biochem., 189, 33 (1990)<br></p>Formula:C4H6O2Color and Shape:NeatMolecular weight:86.095-(Benzyloxy)-2-((benzyloxy)carbonyl)-3-hydroxy-5-oxopentanoic Acid
Controlled Product<p>Applications 5-(Benzyloxy)-2-((benzyloxy)carbonyl)-3-hydroxy-5-oxopentanoic Acid is an intermediate used in the synthesis of 2-[2-[(5-carboxypentyl)amino]-2-oxoethyl]-2-hydroxybutanedioic Acid (C181175), which is derived from Methyl 6-Aminohexanoate Hydrochloride (M287100), which is used as a reagent to synthesize straight chain hydroxamates, compounds that act as inhibitors of Human Histone Deacetylase (HDAC) that have the potential to treat cancer. Methyl 6-aminohexanoate is also sometimes used as a spacer unit for peptide synthesis.<br>References Matthews, S., et al.: J. Chem. Soc. Chem. Commun., 17, 1809 (1995); Remiszewski, S., et al.: J. Med. Chem., 45, 753 (2002)<br></p>Formula:C20H20O7Color and Shape:NeatMolecular weight:372.369(2S)-4-Oxo-2-oxetanecarboxylic Acid
CAS:Controlled ProductFormula:C4H4O4Color and Shape:NeatMolecular weight:116.0723-(3-Furyl)acrylic Acid
CAS:Controlled Product<p>Applications 3-(3-Furyl)acrylic Acid is a reactant in the preparation of 7-aminofuro[2,3-c]pyridine inhibitors of TAK1.<br>References Hornberger, K.R., et. al.: Bioorg. Med. Chem. Lett., 23, 4517 (2013)<br></p>Formula:C7H6O3Color and Shape:NeatMolecular weight:138.123-Phenylisonicotinic Acid
CAS:Controlled Product<p>Applications 3-PHENYLISONICOTINIC ACID (cas# 104096-15-3) is a useful research chemical.<br></p>Formula:C12H9NO2Color and Shape:NeatMolecular weight:199.22-Amino-2-deoxy-D-erythronic Acid
CAS:Controlled ProductFormula:C4H9NO4Color and Shape:NeatMolecular weight:135.119Methyl-3-ethoxyisothiazole-5-carboxylate
CAS:Controlled Product<p>Applications Synthesis and receptor binding of 5-(amino[3H]2methyl)-3-isothiazolol ([3H]thiomuscimol), a specific GABAA agonist photoaffinity label.<br>References Frolund, B., et al.: J. Labelled Compounds Radiopharm., 36, 877 (1995),<br></p>Formula:C7H9NO3SColor and Shape:NeatMolecular weight:187.22(1R,3R,4R,5R)-3,4,5-Trihydroxycyclohexane-1-carboxylic Acid
Controlled ProductFormula:C7H12O5Color and Shape:NeatMolecular weight:176.167Dimethyl-1,3-acetonedicarboxylate
CAS:Controlled Product<p>Applications Dimethyl-1,3-acetonedicarboxylate is used in the preparation of optically active lycorane. It has also been substituted into bispidone derivatives for their use as ligands in PET imaging.<br>References Yoshizaki, H. et al.: J. Org. Chem., 60, 2016 (1995); Legdali, T. et al.: J. Org. Chem., 77, 11167 (2012);<br></p>Formula:C7H10O5Color and Shape:NeatMolecular weight:174.15(1S,3R,4S)-Ethyl 4-Amino-3-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate Oxalate
CAS:Controlled Product<p>Applications (1S,3R,4S)-Ethyl 4-Amino-3-((tert-butoxycarbonyl)amino)cyclohexanecarboxylate Oxalate has been used as a reactant for the preparation of oxadiazole compounds containing cyclohexanediamine moiety.<br></p>Formula:C14H26N2O4·C2H2O4Color and Shape:NeatMolecular weight:376.402trans-1,2-Cyclohexanedicarboxylic Acid
CAS:Controlled Product<p>Applications trans-1,2-Cyclohexanedicarboxylic Acid is used as a reagent in the synthesis of enantiopure (α-cyanoalkyl)(tetrahydropyrido[4,3-b]indolecarbonyl)cyclohexanecarboxamides and its analogs as selective cathepsin K inhibitors for the treatment of osteoarthritis. Also used as a reagent in the synthesis of novel cyclopentanedicarboxamide sodium channel blockers as a potential treatment for chronic pain.<br>References Dossetter, A.G., et al.: J. Med. Chem., 55, 6363 (2012); Shao, P.P., et al.: Bioorg. Med. Chem. Lett., 15, 1901 (2005)<br></p>Formula:C8H12O4Color and Shape:WhiteMolecular weight:172.18Benzyl Acetoacetic Amide
CAS:Controlled Product<p>Applications Benzyl Acetoacetic Amide (cas# 882-36-0) is a compound useful in organic synthesis.<br>References Sakaki, J., et al.: Chem. Pharm. Bull., 37, 2952 (1989),<br></p>Formula:C11H13NO2Color and Shape:NeatMolecular weight:191.231,2,4-Benzenetricarboxylic Acid 2-(2-ethylhexyl) Ester
CAS:Controlled ProductFormula:C17H22O6Color and Shape:NeatMolecular weight:322.353
