61432-55-1

Usage

Uses

Used in Insect Repellent Industry:
Dimepiperate is used as an active ingredient in insect repellent formulations for its effectiveness in repelling insects such as mosquitoes, flies, and ticks. Its mode of action involves disrupting the insects' sensory mechanisms, which inhibits their ability to detect and bite or land on the skin, thereby reducing the risk of insect-borne diseases.
Used in Public Health and Disease Prevention:
Dimepiperate is utilized in public health initiatives to prevent the spread of insect-borne diseases such as malaria, dengue fever, and Lyme disease. By incorporating Dimepiperate into insect repellent products, it helps protect individuals from these potentially serious health threats, especially in regions where these diseases are prevalent.

InChI:InChI=1/C15H21NOS/c1-15(2,13-9-5-3-6-10-13)18-14(17)16-11-7-4-8-12-16/h3,5-6,9-10H,4,7-8,11-12H2,1-2H3

Upstream product

• 110-89-4 piperidine 
• 16325-88-5 α,α-dimethylbenzylmercaptan 
• 13939-69-0 piperidine carbamoyl chloride 

Relevant academic research and scientific papers

Synergistic herbicidal mixtures

PCT No. PCT/EP96/04935 Sec. 371 Date May 1, 1998 Sec. 102(e) Date May 1, 1998 PCT Filed Nov. 12, 1996 PCT Pub. No. WO97/17852 PCT Pub. Date May 22, 1997A synergistically active herbicidal composition which comprises, as active components, a mixture of 1-(3-chloro-4,5,6,7-tetrahydropyrazolo-[1,5-a]-pyridin-2-yl)-5-(methylpropargylamino)-4-pyrazolylcarbonitrile [Component (A)] and a herbicide selected from the group consisting of bentazone, molinate, daimuron, thiobencarb, butachlor, pretilachlor, dimepiperate, fenoxaprop-ethyl, clomeprop, cinmethylin, bromobutide, quinclorac, mefenacet, pyrazosulfuron-ethyl, esprocarb, cinosulfuron, thenylchlor, cumyluron, MK 243, naproanilide, anilofos, benfuresate, bifenox, CH-900, MCPA, nitrofen, oxadiazon, pendimethalin, simetryn, sulcotrione (ICIA0051), trifluralin, piperophos, pyributicarb, ethoxysulfuron, bensulfuronmethyl, pyrazolate, pyrazoxyfen, benzofenap, cyclosulfamuron, cyhalofop-butyl, NBA-061, azimsulfuron, propanil or imazosulfuron [Component (B)] and which are suitable for controlling undesirable plants in rice cultivation.

Synergistic herbicidal mixtures containing cyclohexenone oxime ethers

PCT No. PCT/EP96/04000 Sec. 371 Date Mar. 17, 1998 Sec. 102(e) Date Mar. 17, 1998 PCT Filed Sep. 12, 1996 PCT Pub. No. WO97/10710 PCT Pub. Date Mar. 27, 1997Herbicidal compositions containing a) at least one cyclohexenone oxime ether of the formula I and b) at least one of the following 44 compounds: b1) bromobutide, dimepiperate, etobenzanid, propanil, b2) anilofos, mefenacet, b3) 2,4-D, MCPB, naproanilide, b4) bentazone, b5) pyrazolynate/pyrazolate, sulcotrione, b6) esprocarb, molinate, pyributicarb, thiobencarb/benthiocarb, b7) quinclorac, b8) butachlor, butenachlor, pretilachlor, thenylchlor, b9) cycloxydim, sethoxydim, b10) pendimethalin, b11) cyhalofop-butyl, fenoxaprop-ethyl, b12) benzofenap, pyrazoxyfen, b13) dithiopyr, b14) sodium 2,6-bis[(4,6-dimethoxypyrimidin-2-yl)oxy]-benzoate and methyl 2-[(4,6-dimethoxypyrimidin-2-yl)-oxy]-6-[1-(methoxyimino)ethyl]benzoate; b15) azimsulfuron, bensulfuron-methyl, cinosulfuron, cyclosulfamuron, ethoxysulfuron, imazosulfuron, pyrazosulfuron-ethyl, b16) dimethametryn, simetryn/simetryne, b17) benfuresate, b18) cafenstrole, b19) cinmethylin, b20) piperophos, are described.

Herbicidal tetrazolinones

Novel herbicidal tetrazolinones of the formula STR1 wherein Y is hydrogen, bromine or methyl, R1 is ethyl or n-propyl, and R2 is cyclopentyl or cyclohexyl, with the proviso that the total number of carbon atoms in R1 and R2 is 7 or 8. The new tetrazolinones may be mixed with other herbicides.

Tetrzolinone herbicides

Novel tetrazolinones of the formula (I) STR1 wherein X is chlorine or bromine, Y is hydrogen, chlorine, bromine, methyl or ethyl, and R1 and R2 are the same or different C2-4 alkyl, a process for their preparation, and the use of the new compounds as herbicides, especially against paddy-weeds.

Herbicidal tetrazolinones

Herbicidal novel tetrazolinones of the formula STR1 wherein Y represents hydrogen, chlorine, or methyl, R1 represents ethyl or n-propyl, and R2 represents cyclopentyl or cyclohexyl, with the proviso that the total of the carbon atoms of R1 and R2 is 7 or 8. They may be mixed with other herbicides.

Process for production of thiolcarbamates and the thiolcarbamates obtained by said process

A process for producing a thiolcarbamate compound of the following formula STR1 wherein R1 represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, a halogen atom or a nitro group, R2 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, m is 1 or 2, and n is an integer of 4 to 6, which comprises reacting an α-methylstyrene of the following formula STR2 wherein R1 is as defined above, or its dimer with hydrogen sulfide in the presence of a catalyst to form a mercaptan of the following formula STR3 wherein R1 is as defined above, and reacting the mercaptan of formula (II) with a carbamoyl chloride of the following formula STR4 wherein R2, m and n are as defined.

Process for the production of thiolcarbamate compounds

In the process for the production of a thiolcarbamate compound of the formula STR1 wherein R1 and R2 are as defined in claim, comprising reacting a tertiary halogen compound of the formula STR2 wherein X and R3 are as defined in claim, with a thiolcarbamic acid salt of the formula STR3 wherein M represents a member selected from the group consisting of the alkali metals, ammonium group and immonium group, in an aqueous reaction medium, in the presence of a strong base; the improvement wherein the reaction is carried out under conditions in which the reaction system is adjusted to a pH ranging from about 9 to about 13.