18113-07-0

Basic information

• Product Name: 4-Chloro-3-methoxyphenol
• Synonyms: 4-Chloro-3-methoxyphenol
• CAS NO: 18113-07-0
• Molecular Formula: C₇H₇ClO₂
• Molecular Weight: 158.58228
• Mol File: 18113-07-0.mol
• Article Data: 9

Chemical Properties

• Melting Point: 79-80 °C
• Boiling Point: 141-150 °C(Press: 18 Torr)
• Appearance: /
• Density: 1.280±0.06 g/cm3(Predicted)
• Storage Temp.: Inert atmosphere,Room Temperature
• PKA: 9.14±0.18(Predicted)
• CAS DataBase Reference: 4-Chloro-3-methoxyphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-3-methoxyphenol(18113-07-0)
• EPA Substance Registry System: 4-Chloro-3-methoxyphenol(18113-07-0)

Safety Data

• Hazardous Substances Data: 18113-07-0(Hazardous Substances Data)

Usage

General Description

4-Chloro-3-methoxyphenol, also known as para-chloro-meta-cresol (PCMC), is a chemical compound belonging to the class of chlorophenols. It is a colorless to pale yellow crystalline solid with a slightly phenolic odor. It is widely used as an antiseptic and disinfectant in various industries, including pharmaceuticals, cosmetics, and personal care products. PCMC is effective against a wide range of bacteria and fungi and is commonly used in products such as hand sanitizers, soaps, and surgical scrubs. However,

Upstream product

• 61638-01-5 4-Amino-3-methoxyphenol 
• 13726-14-2 4-chloro-m-anisidine 
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• 1009-36-5 2-chloro-5-nitroanisole 
• 49735-71-9 2-methoxy-4-nitrobenzene diazonium 1,5-naphthalene disulfonate 
• 95-88-5 4-Chlororesorcinol 
• 74-88-4 methyl iodide 
• 89694-47-3 (4-chloro-3-methoxyphenyl)boronic acid 

Downstream Products

• 7051-13-0 1-chloro-2,4-dimethoxybenzene 
• 111478-42-3 3-(4-chloro-3-methoxyphenoxy)butyric acid 
• 26378-26-7 4-(2-Bromo-ethoxy)-1-chloro-2-methoxy-benzene 
• 26378-43-8 [2-(4-Chloro-3-methoxy-phenoxy)-ethyl]-dimethyl-amine 
• 26378-45-0 [2-(4-Chloro-3-methoxy-phenoxy)-ethyl]-diethyl-amine 
• 403657-31-8 Formaldehyde bis(4-chloro-3-methoxyphenyl)acetal 
• 26378-41-6 2-(4-Chloro-3-methoxy-phenoxy)-ethylamine 
• 26378-47-2 5-(2-Amino-ethoxy)-2-chloro-phenol 
• 26378-49-4 2-Chloro-5-(2-dimethylamino-ethoxy)-phenol 
• 26378-51-8 2-Chloro-5-(2-diethylamino-ethoxy)-phenol 
• 181648-42-0 tert-butyl-(4-chloro-3-methyl-phenoxy)-dimethyl-silane 
• 89938-56-7 5-chloro-2-hydroxy-4-methoxy-benzaldehyde 
• 1309612-66-5 C₂₆H₂₄ClN₃O₆ 

Relevant articles and documents

Derivatives of m-Guaiacol, Their Preparation and Their Uses

The invention concerns derivatives of m-guaiacol, their preparation and their uses as biocides, in particular as antibacterials or disinfectants.

SUBSTITUTED-N-HETEROARYL COMPOUNDS AND USES THEREOF

The present disclosure relates generally to compounds useful for the treatment and/or enhancement of cognitive function and negative symptoms associated with central nervous system disorders where the circuitry involving fast spiking PV+ interneurons and the production of cortical gamma oscillations is disrupted. The subject disclosure enables the manufacture of medicaments as well as compositions containing same for use in methods of therapy and prophylaxis of cognitive dysfunction and negative symptoms.

A photochemical route to 2-substituted benzo[b]furans

2-Substituted benzo[b]furans were synthesized by a one-step metal-free photochemical reaction between 2-chlorophenol derivatives and terminal alkynes by tandem formation of an aryl-C and a C-O bond via an aryl cation intermediate. The mild conditions and the application to chlorophenols rather of the more expensive bromo or iodo analogues makes this procedure environmentally convenient.