CAS 1914-65-4
:1,2,3,4-Tetrahydro-1-naphthoic acid
Description:
1,2,3,4-Tetrahydro-1-naphthoic acid is an organic compound characterized by its bicyclic structure, which consists of a naphthalene ring system that has undergone partial hydrogenation. This compound features a carboxylic acid functional group, contributing to its acidic properties. It is typically a white to off-white solid at room temperature and is soluble in organic solvents, but its solubility in water is limited due to its hydrophobic naphthalene structure. The presence of the tetrahydro moiety indicates that it has four hydrogen atoms added to the naphthalene framework, which affects its reactivity and physical properties. 1,2,3,4-Tetrahydro-1-naphthoic acid is often used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Its derivatives can exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.
Formula:C11H12O2
InChI:InChI=1/C11H12O2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-2,4,6,10H,3,5,7H2,(H,12,13)
SMILES:c1ccc2c(c1)CCCC2C(=O)O
Synonyms:- 1,2,3,4-Tetrahydro-Naphthalene-1-Carboxylic Acid
- 1,2,3,4-Tetrahedro-Naphthoic Acid
- 1,2,3,4-TETRAHYDRO-1-NAPHTHOIC ACID
- 1-Tetralincarboxylic acid
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Found 11 products.
1,2,3,4-Tetrahydronaphthalene-1-carboxylic Acid
CAS:Formula:C11H12O2Purity:>98.0%(GC)(T)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:176.221,2,3,4-Tetrahydro-1-naphthoic acid, 98%
CAS:<p>1,2,3,4-Tetrahydro-1-naphthoic acid is used as an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. 1,2,3,4-tetrahydronaphthalene-1-carboxylic acid is a reagent used to produce protease inhibitors. This Thermo Scientific Chemicals brand</p>Formula:C11H12O2Purity:98%Color and Shape:White to pale cream, PowderMolecular weight:176.22Tetrahydrozoline Related Compound C (1,2,3,4-Tetrahydronaphthalene-1-carboxylic acid)
CAS:Aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacid and their derivatives not elsewhere specified or includedFormula:C11H12O2Color and Shape:White SolidMolecular weight:176.083731-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-
CAS:Formula:C11H12O2Purity:98%Color and Shape:SolidMolecular weight:176.21181,2,3,4-Tetrahydro-1-naphthalenecarboxylic Acid
CAS:Controlled ProductFormula:C11H12O2Color and Shape:NeatMolecular weight:176.211,2,3,4-Tetrahydro-1-naphthoic acid
CAS:<p>1,2,3,4-Tetrahydro-1-naphthoic acid</p>Purity:97%Molecular weight:176.21g/mol1,2,3,4-Tetrahydro-1-naphthoic Acid
CAS:Controlled Product<p>Applications Reagent used to produce protease inhibitors.<br>References Zhu, Y., et al.: J. Med. Chem., 52, 4192 (2009),<br></p>Formula:C11H12O2Color and Shape:WhiteMolecular weight:176.211,2,3,4-Tetrahydronaphthalene-1-carboxylic acid
CAS:Formula:C11H12O2Purity:95%Color and Shape:White – Slightly pale reddish yellow powderMolecular weight:176.2151,2,3,4-Tetrahydro-1-naphthoic acid
CAS:<p>Tetrahydro-1-naphthoic acid is a toxic chemical that is used in the synthesis of various organic compounds. It is an organic acid that has a pungent odor and can cause irritation of the nose and throat. When heated, it evolves toxic fumes of hydrogen chloride gas and phosgene. Tetrahydro-1-naphthoic acid reacts with metal hydroxides to form metal tetrahydro-1-naphthoates, which have useful properties as catalysts in organic reactions. Tetrahydro-1-naphthoic acid has been used as a growth regulator in plants and animals. It binds to DNA at the C–H site, preventing protein synthesis and cell division by inhibiting RNA synthesis.</p>Formula:C11H12O2Purity:Min. 95%Molecular weight:176.21 g/mol











