78444-53-8

Basic information

• Product Name: 2,4-dichloro-N-(1-hydroxy-2-methylpropan-2-yl)-6-methoxybenzamide
• Synonyms: 2,4-dichloro-N-(1-hydroxy-2-methylpropan-2-yl)-6-methoxybenzamide
• CAS NO: 78444-53-8
• Molecular Weight: 292.162
• Mol File: 78444-53-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,4-dichloro-N-(1-hydroxy-2-methylpropan-2-yl)-6-methoxybenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dichloro-N-(1-hydroxy-2-methylpropan-2-yl)-6-methoxybenzamide(78444-53-8)
• EPA Substance Registry System: 2,4-dichloro-N-(1-hydroxy-2-methylpropan-2-yl)-6-methoxybenzamide(78444-53-8)

Safety Data

• Hazardous Substances Data: 78444-53-8(Hazardous Substances Data)

Usage

General Description

2,4-dichloro-N-(1-hydroxy-2-methylpropan-2-yl)-6-methoxybenzamide is a chemical compound with the molecular formula C12H14Cl2N2O3. It is a derivative of 2,4-Dichlorophenoxyacetic acid (2,4-D), which is a widely used herbicide. 2,4-dichloro-N-(1-hydroxy-2-methylpropan-2-yl)-6-methoxybenzamide is commonly used in the agricultural industry to control the growth of broadleaf weeds in various crops. It works by mimicking the plant hormone auxin and disrupting the normal function of plant growth, leading to the death of unwanted plants. When used according to regulations, this chemical has shown to be an effective and safe herbicide for crop protection. However, proper handling, storage, and disposal procedures should be followed to prevent any negative impact on the environment and human health.

Upstream product

• 94294-09-4 2,4-dichloro-6-methoxybenzoic acid 
• 78443-72-8 4,6-dichlorosalicylaldehyde 
• 124-68-5 2-Amino-2-methyl-1-propanol 
• 99725-35-6 2,4-dichloro-6-methoxybenzoic acid chloride 
• 78444-52-7 2,4-dichloro-6-methoxybenzaldehyde 

Downstream Products

• 99725-38-9 2-<2,4-dichloro-6-(2-phenylethyl)phenyl>-4,5-dihydro-4,4-dimethyloxazole 
• 78444-54-9 2-(2,4-dichloro-6-methoxyphenyl)-4,5-dihydro-4,4-dimethyloxazole 

Relevant articles and documents

6-substituted-4-hydroxytetrahydropyran-2-one derivatives and pharmaceutical compositions containing them

The present invention provides compounds of the general formula: STR1 wherein E is an alkylene or alkenylene radical containing 2 carbon atoms, R1 is a cycloaliphatic hydrocarbon radical containing 5 to 12 carbon atoms, which is optionally subs

Substituted pyranone inhibitors of cholesterol synthesis

The methyl, ethyl, n-propy, 2-(acetylamino)ethyl, or 1-(2,3-dihydroxy)propyl ester of E-(3R,5S)-7-(4'-fluoro-3,3',5-trimethyl[1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acid of structural formula: STR1 are HMG-CoA reductase inhibitors useful in the treatment of conditions associated with hypercholesterolemia.

SUBSTITUTED PYRANONE INHIBITORS OF CHOLESTEROL SYNTHESIS

6-Phenyl-, phenylalkyl-and phenylethenyl-4-hydroxytetrahydropyran-2-ones in the 4(R)-trans stereoisomeric forms are potent inhibitors of cholesterol synthesis by virtue of their ability to inhibit the enzyme, 3-hydroxy-3-methylglutaryl-coenzyme A reductas