43067-49-8

Basic information

• Product Name: 1,1-Di(4-chlorophenoxy)-3,3-dimethylbutan-2-one
• Synonyms: 1,1-Di(4-chlorophenoxy)-3,3-dimethylbutan-2-one
• CAS NO: 43067-49-8
• Molecular Formula: C₁₈H₁₈Cl₂O₃
• Molecular Weight: 353.24
• Mol File: 43067-49-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,1-Di(4-chlorophenoxy)-3,3-dimethylbutan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-Di(4-chlorophenoxy)-3,3-dimethylbutan-2-one(43067-49-8)
• EPA Substance Registry System: 1,1-Di(4-chlorophenoxy)-3,3-dimethylbutan-2-one(43067-49-8)

Safety Data

• Hazardous Substances Data: 43067-49-8(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

1,1-Di(4-chlorophenoxy)-3,3-dimethylbutan-2-one is derived from butan-2-one, which is a simple ketone with a four-carbon chain.

Explanation

The compound has two 4-chlorophenoxy groups attached to its structure, which are responsible for its herbicidal properties.

Explanation

It is commonly used as a herbicide to selectively control broadleaf weeds in various crops.

Explanation

The compound works by inhibiting the growth of unwanted plants and disrupting their cellular processes, leading to their death.

Explanation

If ingested or inhaled, 1,1-Di(4-chlorophenoxy)-3,3-dimethylbutan-2-one can be harmful to humans and animals, so it should be handled with care.

Explanation

Due to its potential toxicity, it is important to follow safety guidelines and precautions when handling this chemical compound.

Derivative of butan-2-one

Yes

Contains 4-chlorophenoxy groups

Two

Contains methyl groups

Two

Application

Herbicide

Mode of action

Inhibits growth and disrupts cellular processes

Toxicity

Can be toxic to humans and animals

Safety precautions

Handle with care

Upstream product

• 141-78-6 ethyl acetate 
• 106-48-9 4-chloro-phenol 

Downstream Products

• 91171-10-7 1,1-Bis-(4-chloro-phenoxy)-3,3-dimethyl-butan-2-ol 
• 91171-22-1 1,1-Bis-(4-chlorophenoxy)-3,3-dimethylbut-1-ene 
• 91171-16-3 Toluene-4-sulfonic acid 1-[bis-(4-chloro-phenoxy)-methyl]-2,2-dimethyl-propyl ester 

Relevant articles and documents

1-Substituted-1,2,4-triazole fungicidal compositions and methods for combatting fungi that infect or attack plants

1-SUBSTITUTED-1,2,4-TRIAZOLES OF THE FORMULA STR1 in which X1 represents hydrogen or an alkyl radical, X2 represents hydrogen or an alkyl radical, R1 represents an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, R2 represents hydrogen or an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, R3 represents hydrogen or an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, and Y represents a keto group or a functional keto derivative, which possess fungicidal properties.

1,2,4-Triazole antimycotic compositions and use thereof

Antimycotic compositions are produced which comprise an antimycotically effective amount of a 1,2,4-triazole of the formula: STR1 or a pharmaceutically acceptable non-toxic salt thereof wherein X1 is hydrogen or alkyl; X2 is hydrogen or alkyl; R1 is alkyl, unsubstituted or substituted aryl or unsubstituted or substituted aralkyl; R2 is hydrogen, alkyl or unsubstituted or substituted aryl; R3 is alkyl, cycloalkyl, unsubstituted or substituted aryl or unsubstituted or substituted aralkyl; and Y is a keto group of a functional derivative of a keto group, in combination with a pharmaceutically acceptable non-toxic, inert diluent or carrier.

1-Substituted-1,2,4-triazole fungicides

1-Substituted-1,2,4-triazoles of the formula STR1 in which X1 represents hydrogen or an alkyl radical, X2 represents hydrogen or an alkyl radical, R1 represents an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, R2 represents hydrogen or an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, R3 represents hydrogen or an alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl or optionally substituted aryl or aralkyl radical, and Y represents a keto group or a functional keto derivative, Which possess fungicidal properties.