85785-20-2

Basic information

• Product Name: ESPROCARB
• Synonyms: (1,2-dimethylpropyl)ethyl-carbamothioicacis-(phenylmethyl)ester;s-(phenylmethyl)(1,2-dimethylpropyl)ethylcarbamothioate;s-benzyln-ethyl-n-(1,2-dimethylpropyl)thiocarbamate;sc2957;S-BENZYL 1,2-DIMETHYLPROPYL(ETHYL)THIOCARBAMATE;FUJIGRASS;ESPROCARB;S-(phenylmethyl) (1,2-dimethylpropyl)ethylthiocarbamate
• CAS NO: 85785-20-2
• Molecular Formula: C15H23NOS
• Molecular Weight: 265.41
• Mol File: 85785-20-2.mol

Chemical Properties

• Melting Point: <25℃
• Boiling Point: 357.4°Cat760mmHg
• Flash Point: 170°C
• Appearance: /
• Density: 1.0566 (rough estimate)
• Vapor Pressure: 2.73E-05mmHg at 25°C
• Refractive Index: 1.7500 (estimate)
• Storage Temp.: 0-6°C
• PKA: -1.32±0.70(Predicted)
• CAS DataBase Reference: ESPROCARB(CAS DataBase Reference)
• NIST Chemistry Reference: ESPROCARB(85785-20-2)
• EPA Substance Registry System: ESPROCARB(85785-20-2)

Safety Data

• Hazard Codes: N
• Statements: 51/53
• Safety Statements: 60
• RIDADR: UN3082 9/PG 3
• WGK Germany: 2
• RTECS: FD3830000
• Hazardous Substances Data: 85785-20-2(Hazardous Substances Data)

Usage

Uses

Used in Pesticide Industry:
ESPROCARB is used as a synergist in pesticidal compositions to enhance the effectiveness of active ingredients. It helps in improving the delivery of these active ingredients, ensuring a more efficient and targeted approach to pest control. This results in better pest management and reduced chemical usage, ultimately benefiting both the environment and agricultural productivity.

InChI:InChI=1/C15H23NOS/c1-5-16(13(4)12(2)3)15(17)18-11-14-9-7-6-8-10-14/h6-10,12-13H,5,11H2,1-4H3

Upstream product

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• 37734-45-5 benzyl chlorothioformate 

Relevant articles and documents

HERBICIDAL COMPOSITIONS

The present invention provides compositions comprising herbicidally active compounds (A) and (B), where (A) represents one or more compounds of the general formula (I) or agrochemically compatible salts thereof [component (A)], and (B) represents one or more herbicides [component (B)]. The application further relates to a method and to the use of the herbicidal composition according to the invention for controlling harmful plants or for regulating growth.

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.

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.

S-benzyl thiolcarbamates and their use in controlling weeds in rice fields

Novel S-benzyl thiolcarbamates are disclosed, having the formula STR1 in which R1 is selected from the group consisting of hydrogen and methoxy, R2 is selected from the group consisting of methyl, ethyl, and allyl, and R3