CAS 606-40-6
:2-chloronaphthalen-1-ol
Description:
2-Chloronaphthalen-1-ol, with the CAS number 606-40-6, is an organic compound that belongs to the class of chlorinated naphthalenes. It features a naphthalene ring system substituted with a hydroxyl group (-OH) and a chlorine atom at the 2-position. This compound typically appears as a solid at room temperature and is characterized by its aromatic structure, which contributes to its stability and potential reactivity. 2-Chloronaphthalen-1-ol is known for its applications in organic synthesis and as an intermediate in the production of various chemicals. It exhibits moderate solubility in organic solvents and limited solubility in water, reflecting its hydrophobic nature due to the naphthalene backbone. The presence of both the hydroxyl and chlorine groups can influence its chemical behavior, including its reactivity in nucleophilic substitution reactions and its potential as a ligand in coordination chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks upon exposure.
Formula:C10H7ClO
InChI:InChI=1/C10H7ClO/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-6,12H
SMILES:c1ccc2c(c1)ccc(c2O)Cl
Synonyms:- 1-Naphthalenol, 2-chloro-
- 2-Chloro-1-naphthalenol
- 2-Chloro-1-Naphthol
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Found 2 products.
2-Chloro-1-naphthol
CAS:<p>2-Chloro-1-naphthol</p>Formula:C10H7ClOPurity:97%Color and Shape: faint red crystalline solidMolecular weight:178.61g/mol2-Chloronaphthalen-1-ol
CAS:<p>2-Chloronaphthalen-1-ol is a molecule that has been studied as a possible therapeutic agent for autoimmune diseases. This compound binds to the pd-l1 receptor, which is associated with autoimmune diseases. 2-Chloronaphthalen-1-ol also binds to monoclonal antibodies, which are used in diagnostic procedures and histochemical staining of biological samples. The reactive functional group on this molecule allows it to bind to other molecules through covalent bonds, which can lead to structural analysis and diagnosis of certain diseases.<br>2-Chloronaphthalen-1-ol is an organic compound that belongs to the class of naphthalene derivatives. It has a reactive functional group that allows it to form covalent bonds with other molecules. This property has made it an important model system for studying reactive functional groups in chemical reactions and for diagnostic purposes in immunology and histochemistry.</p>Formula:C10H7ClOPurity:Min. 95%Molecular weight:178.61 g/mol

