18327-79-2

Basic information

• Product Name: (2,4-DI-TERT-BUTYLPHENOXY)ACETIC ACID
• Synonyms: (2,4-di-tert-butylphenoxy)acetate
• CAS NO: 18327-79-2
• Molecular Formula: C₁₆H₂₄O₃
• Molecular Weight: 264.37
• Mol File: 18327-79-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 361.7°Cat760mmHg
• Flash Point: 123.1°C
• Appearance: /
• Density: 1.024g/cm³
• Vapor Pressure: 7.28E-06mmHg at 25°C
• CAS DataBase Reference: (2,4-DI-TERT-BUTYLPHENOXY)ACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (2,4-DI-TERT-BUTYLPHENOXY)ACETIC ACID(18327-79-2)
• EPA Substance Registry System: (2,4-DI-TERT-BUTYLPHENOXY)ACETIC ACID(18327-79-2)

Safety Data

• Hazardous Substances Data: 18327-79-2(Hazardous Substances Data)

Usage

General Description

(2,4-DI-TERT-BUTYLPHENOXY)ACETIC ACID, also known as Dicamba, is a herbicide widely used to control broadleaf weeds in various agricultural crops. It works by mimicking the plant hormone auxin, causing uncontrolled, unsustainable growth in the target plants, ultimately leading to their death. Dicamba is a selective herbicide, meaning it primarily targets broadleaf weeds while leaving grasses and other non-target plants relatively unharmed. It is commonly used in combination with other herbicides to provide effective and comprehensive weed control. However, due to its potential to drift and cause damage to neighboring crops and vegetation, its use has been controversial and highly regulated in some regions.

InChI:InChI=1/C16H24O3/c1-15(2,3)11-7-8-13(19-10-14(17)18)12(9-11)16(4,5)6/h7-9H,10H2,1-6H3,(H,17,18)/p-1

Upstream product

• 96-76-4 2,4-di-tert-Butylphenol 
• 934130-78-6 C₁₈H₂₈O₃ 
• 1435933-49-5 C₂₀H₃₂O₃ 
• 79-11-8 chloroacetic acid 

Downstream Products

• 1435933-40-6 C₂₄H₃₅N₃O₃ 

Relevant articles and documents

Solid-phase oxidation of 2,4-di-tert-butylphenol and 3,6-di-tert-butylpyrocatechol in the presence of alkali and alkaline earth metal halides under elastic deformation

Solid-phase oxidation of 2,4-di-tert-butylphenol to give 2,2′,4,4′-tert-butyl-6,6′-bisphenol and of 3,6-di-tert-butylpyrocatechol to afford 3,6-di-tert-butyl-1,2-benzoquinone was performed in the presence of alkali and alkaline earth metals halides under conditions of modified extrusion. The formation of the corresponding metal 3,6-di-tert-butylsemiquinolates was registered by ESR method. The different behavior of chlorides, bromides, and iodides was observed and rationalized basing on the dissimilar complexing ability of halogens. The mechanism of activated oxidation was assumed.

Discovery of potent transient receptor potential vanilloid 1 antagonists: Design and synthesis of phenoxyacetamide derivatives

We aimed to discover a novel type of transient receptor potential vanilloid 1 (TRPV1) antagonist because such antagonists are possible drug candidates for treating various disorders. We modified the structure of hit compound 7 (human TRPV1 IC50 = 411 nM) and converted its pyrrolidino group to a (hydroxyethyl)methylamino group, which substantially improved inhibitory activity (15d; human TRPV1 IC50 = 33 nM). In addition, 15d ameliorated bladder overactivity in rats in vivo.