361212-70-6

Basic information

• Product Name: [2-(2,4-DICHLOROPHENOXY)PHENYL]METHANOL
• Synonyms: [2-(2,4-DICHLOROPHENOXY)PHENYL]METHANOL
• CAS NO: 361212-70-6
• Molecular Formula: C₁₃H₁₀Cl₂O₂
• Molecular Weight: 269.12
• Mol File: 361212-70-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 61-63°C
• Appearance: /
• CAS DataBase Reference: [2-(2,4-DICHLOROPHENOXY)PHENYL]METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: [2-(2,4-DICHLOROPHENOXY)PHENYL]METHANOL(361212-70-6)
• EPA Substance Registry System: [2-(2,4-DICHLOROPHENOXY)PHENYL]METHANOL(361212-70-6)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 361212-70-6(Hazardous Substances Data)

Usage

General Description

[2-(2,4-DICHLOROPHENOXY)PHENYL]METHANOL is a chemical compound that belongs to the group of phenols, which are organic compounds that contain a hydroxyl group attached to an aromatic hydrocarbon group. It is specifically derived from 2,4-dichlorophenol, a common ingredient in herbicides and insecticides. The compound has a molecular formula C13H10Cl2O2 and a molecular weight of 269.12 g/mol. It is used for a variety of industrial applications, including as a chemical intermediate in the production of pharmaceuticals, solvents, and dyes. The compound may also have potential environmental and health implications due to its toxicity and persistence in the environment.

Upstream product

• 120-82-1 1,2,4-Trichlorobenzene 
• 120-83-2 2,4-dichlorophenol 
• 446-52-6 2-Fluorobenzaldehyde 
• 175136-80-8 2-(2,4-dichlorophenoxy)benzonitrile 
• 7681-38-1 sodium hydrogen sulfate 
• 96042-30-7 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran 
• 86309-06-0 2-(2,4-dichlorophenoxy)benzaldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 
• 3757-76-4 sodium 2,4-dichlorophenolate 
• 33838-32-3 potassium 2-formylphenolate 

Downstream Products

• 866950-90-5 C₁₅H₁₃Cl₂NO₂S 
• 1393639-45-6 C₁₅H₁₂Cl₂O₃S 
• 1393639-36-5 C₁₄H₁₂Cl₂N₂OS 
• 86308-91-0 <2-(2,4-dichlorophenoxy)phenyl>acetohydroxamic acid 
• 86308-89-6 3-<2-(2,4-dichlorophenoxy)phenyl>propionic acid 
• 70458-41-2 <2-(2,4-dichlorophenoxy)phenyl>acetyl chloride 
• 86308-88-5 2-<2-(2,4-dichlorophenoxy)phenyl>ethanol 
• 34645-84-6 fenclofenac 
• 478032-58-5 2,4-Dichloro-1-(2-chloromethyl-phenoxy)-benzene 

Relevant articles and documents

Wake-promoting agents: Search for next generation modafinil: Part IV

In search of a next generation molecule to the novel wake promoting agent modafinil, a series of diphenyl ether derived wakefulness enhancing agents (in rat) was developed. From this work, racemic compound 16 was separated into its chiral enantiomers to p

Substituted (2-Phenoxyphenyl)acetic Acids with Antiinflammatory Activity. 1

The synthesis and antiinflammatory activity of a series of substituted (2-phenoxyphenyl)acetic acids are described.Initial screening in the adjuvant arthritis test showed that halogen substitution in the phenoxy ring enhanced activity considerably.Ulcerogenic potential, as measured by the minimum ulcerogenic dose (MUD), was low in almost all the acids tested. acetic acid possessed the most favorable combination of potency with low toxicity, including ulcerogenicity, and this compound is now in therapeutic use.