2210-73-3

Basic information

• Product Name: 2-[(4-chloro-2-methylphenoxy)methyl]oxirane
• CAS NO: 2210-73-3
• Molecular Formula: C₁₀H₁₁ClO₂
• Molecular Weight: 198.6461
• Mol File: 2210-73-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 289.2°C at 760 mmHg
• Flash Point: 117.6°C
• Density: 1.226g/cm³
• Vapor Pressure: 0.00388mmHg at 25°C
• Refractive Index: 1.548
• CAS DataBase Reference: 2-[(4-chloro-2-methylphenoxy)methyl]oxirane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-chloro-2-methylphenoxy)methyl]oxirane(2210-73-3)
• EPA Substance Registry System: 2-[(4-chloro-2-methylphenoxy)methyl]oxirane(2210-73-3)

Safety Data

• Hazardous Substances Data: 2210-73-3(Hazardous Substances Data)

Usage

Chemical class

Synthetic pyrrole insecticide and acaricide

Physical form

White crystalline solid

Mode of action

Pro-insecticide, metabolized within the target pest to form the active compound that disrupts the pest's cellular respiration

Effective against

Ants, cockroaches, termites, and bed bugs

Mammalian toxicity

Low

Environmental impact

Relatively low

Usage

Commonly used in agricultural and residential settings

Safety precautions

Use with caution and follow safety guidelines to minimize potential risks to humans and non-target organisms.

Upstream product

• 1570-64-5 2-methyl-4-chlorophenol 
• 857230-93-4 1-chloro-3-(4-chloro-2-methyl-phenoxy)-propan-2-ol 
• 106-89-8 epichlorohydrin 

Downstream Products

• 50714-45-9 4-{2-[3-(4-Chloro-2-methyl-phenoxy)-2-hydroxy-propylamino]-ethoxy}-benzamide 
• 72742-73-5 1-(4-chloro-2-methylphenoxy)-3-[[2-(3-indolyl)-1,1-dimethylethyl]amino]-2-propanol 
• 14556-48-0 1-tert-Butylamino-3-(4-chloro-2-methyl-phenoxy)-propan-2-ol 

Relevant articles and documents

Antihypertensive indole derivatives of phenoxypropanolamines with β-adrenergic receptor antagonist and vasodilating activity

A series of 25 aryloxypropanolamines containing the 3-indolyl-tert-butyl[i.e., 1,1-dimethyl-2-(1H-indol-3-yl)ethyl] or substituted 3-indolyl-tert-butyl moiety as the N substituent is reported. These compounds have been tested for antihypertensive activity in spontaneously hypertensive rats (SHR), β-adrenergic receptor antagonist action in conscious normotensive rats, vasodilating activity in ganglion-blocked rats with blood pressure maintained by angiotensin II infusion, and for intrinsic sympathomimetic action (ISA) in reserpinized rats. Some of the compounds exhibit antihypertensive activity in combination with β-adrenergic receptor antagonist and vasodilating action. The structure-activity relationships in these tests are discussed.