3-(Dichloroacetyl)-2,2,5-trimethyloxazolidine Basic Product Information

Product Name	3-(Dichloroacetyl)-2,2,5-trimethyloxazolidine	CAS	52836-31-4
Synonyms	Oxazolidine,3-(dichloroacetyl)-2,2,5-trimethyl- (9CI);2,2,5-Trimethyl-3-(dichloroacetyl)-1,3-oxazolidine;2,2,5-Trimethyl-3-(dichloroacetyl)oxazolidine; R 29148	Molecular Formula	C8H13 Cl2 N O2
EINECS Number	258-214-7	Molecular Structure
Appearance	Light Yellow Powder
Purity
Supply Ability

3-(Dichloroacetyl)-2,2,5-trimethyloxazolidine Quality documents

3-(Dichloroacetyl)-2,2,5-trimethyloxazolidine Appearance/Package/Shipping/Storage

package

storage condition

Store in cool & dry place,Keep away from strong light and heat

3-(Dichloroacetyl)-2,2,5-trimethyloxazolidine Application

3-(Dichloroacetyl)-2,2,5-trimethyloxazolidine literature

Herbicidal emulsion compositions

-

, (2008/06/13)

A herbicidal emulsion composition comprising an ethenylamide compound as a herbicidally active component and a dichloroacetamide compound as a phytotoxicity reducing agent. This composition has excellent keeping stability because the phytotoxicity reducing agent of the composition does not decompose and crystals do not separate out even when it is kept for a long time. An amino alcohol and a polar nonaqueous solvent as a solvent are added to the ethenylamide compound and the dichloroacetamide compound to prepare a herbicidal emulsion composition.

Herbicide antidotes as safeners for reducing phytotoxicity resulting from synergistic interaction between herbicides and other pesticides

-

, (2008/06/13)

The disclosure herein relates to means for combatting the adverse phytotoxic action to crops arising from the interaction of various herbicidal compounds and biocidal compounds, e.g., insecticidal and/or fungicidal compounds. The means employed to reduce said interaction involves the safening action of various antidotal compounds.

Hydroxyacetyl oxazolidine herbicidal antidotes

-

, (2008/06/13)

Compounds having the formula STR1 in which R₁ -R₄ are each independently selected from the group consisting of hydrogen and alkyl having 1-4 carbon atoms protect corn from thiolcarbamate herbicidal injury.

N-acylation of oxazolidines

-

, (2008/06/13)

N-substituted oxazolidines having the formula STR1 in which R is C₁ -C₁₀ haloalkyl, C₁ -C₁₀ alkyl or lower alkylthio; and R₁ and R₂ are independently hydrogen, C₁ -C₁₂ alkyl, lower alkoxyalkyl or lower alkylol; and R₃, R₄, R₅ and R₆ are independently hydrogen, lower alkyl, lower alkoxyalkyl or lower alkylol are prepared by reacting an oxazolidine with an acid chloride or analogous compound in the presence of a hydrogen chloride acceptor and water. The process is characterized by minimization of by-product formation. In a preferred embodiment, the oxazolidine is prepared by reaction of an alkanolamine with an aldehyde or ketone and the water of reaction is retained in the system.

3-(Dichloroacetyl)-2,2,5-trimethyloxazolidine Upstream and downstream

52836-31-4 Upstream product

• 79-36-7

  dichloroacethyl chloride 

• 52837-54-4

  2,2,5-trimethyl-2,3,4,5-tetrahydroisoxazole 

52836-31-4 Downstream Products

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