131401-55-3

Usage

Chemical Structure

Benzene ring with two fluorine atoms (2,5-difluoro) attached and two ethyl groups (diethyl) attached to the nitrogen atom in the amide functional group.

Functionality

Amide derivative of benzene.

Properties

Appearance: May vary depending on form (liquid, solid).
Odor: Varies depending on formulation and concentration.
Solubility: Varies depending on the solvent, typically soluble in organic solvents.
Melting Point: Dependent on purity and crystalline form.
Boiling Point: Dependent on purity and environmental conditions.

Application

Insect Repellent: Particularly effective against mosquitoes and biting insects.

Mode of Action

Interferes with the insect's ability to detect and locate human hosts.

Commercial Use

Commonly found in commercial insect repellent products.

Safety

Generally considered safe and effective for protecting against insect bites when used as directed.

Effectiveness

Known to be effective in repelling insects, including mosquitoes, when properly applied.

Regulation

Subject to regulatory oversight depending on the jurisdiction and specific use case.

Environmental Impact

Minimal adverse effects when used according to instructions; may have implications for non-target organisms if misused or overused.

Efficacy

Demonstrated efficacy in repelling insects, with varying degrees of effectiveness depending on concentration and formulation.

Upstream product

• 35730-09-7 2,5-difluorobenzoyl chloride 

Downstream Products

• 131401-56-4 2-<(diethylamino)carbonyl>-3,6-difluorobenzoic acid 
• 1416074-03-7 3,6-difluorophtalimide 
• 131401-58-6 3,6-difluoro-2-(2',5'-dimethoxybenzyl)benzoic acid 
• 131401-54-2 1,4-Difluoro-5,8-dihydroxyanthracene-9,10-dione 
• 69895-68-7 1,4-bis {[2-(dimethylamino)ethyl]amino}anthracene-9,10-dione 
• 651-97-8 3,6-difluoro phthalic acid 

Relevant academic research and scientific papers

1,4,8,11,15,18,22,25-octafluorophthalocyaninato zinc (F8PcZn)

1,4,8,11,15,18,22,25-Octafluorophthalocyanato zinc (F8PcZn), which is not described in the literature up to date, was obtained from 3,6-difluorophthalonitrile in anhydrous DMF, DBU, and Zn(OAc)2 at 145°C. 3,6-Difluorophthalonitrile w

Fungicides for the control of take-all disease of plants

A method of controlling Take-All disease of plants by applying a fungicide of the formula STR1 wherein Z1 and Z2 are C and are part of an aromatic ring which is benzothiophene; and A is selected from --C(X)-amine wherein the amine is an unsubstituted, monosubstituted or disubstituted amino radical, --C(O)--SR3, --NH--C(X)R4, and --C(=NR3)--XR7 ; B is --Wm --Q(R2)3 or selected from O-tolyl, 1-naphthyl, 2-naphthyl, and 9-phenanthryl, each optionally substituted with halogen or R4 ; Q is C, Si, Ge, or Sn; W is --C(R3)p H(2-p) --; or when Q is C, W is selected from --C(R3)p H(2-p), --N(R3)m H(1-m)--, --S(O)p--, and --O--; X is 0 or S; n is 0, 1, 2, or 3; m is 0 or 1; p is 0, 1, or 2; each R and R2 is independently defined herein; R3 is C1 -C4 alkyl; R4 is C1 -C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino; and R7 is C1 -C4 alkyl, haloalkyl, or phenyl, optionally substituted with halo, nitro, or R4 ; or an agronomic salt thereof.

The Synthesis of 1,4-Difluoro-5,8-dihydroxyanthracene-9,10-dione and Ipso Substitutions of the Fluorides by Diamines Leading to 1,4-Bis--5,8-dihydroxyanthracene-9,10-diones

Two synthetic pathways to 1,4-difluoro-5,8-dihydroxyanthracene-9,10-dione (2) are described.The ipso substitution of the fluorides of 2 by diamines is a valuable preparative route to 1,4-bis-5,8-dihydroxyanthracene-9,10-diones related t