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N-((4-Chlorophenyl)methyl)-N-cyclopentyl-N'-phenylurea, also known as Pencycuron, is a urea-based fungicide specifically developed to target plant pathogens such as Rhizoctonia solani and Pellicularia spp. It is a non-systemic phenyl urea herbicide that acts by inhibiting cell division in the targeted pathogens. Pencycuron is not highly toxic to mammals but is moderately toxic to birds, most aquatic organisms, honeybees, and earthworms.

66063-05-6

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66063-05-6 Usage

Uses

Used in Agricultural Applications:
Pencycuron is used as a fungicide for controlling diseases caused by Rhizoctonia solani and Pellicularia spp. in various crops. It is effective against these pathogens in potatoes, rice (sheath blight), cotton, sugar beet, vegetables, ornamentals, and turf. The fungicide can be applied to foliage or incorporated into the soil to provide protection against the targeted diseases.
Used in Potato Industry:
N-((4-Chlorophenyl)methyl)-N-cyclopentyl-N'-phenylurea is used as a fungicide for controlling diseases caused by Rhizoctonia solani and Pellicularia spp. in potatoes. This helps in reducing crop losses and improving the overall yield and quality of the potatoes.
Used in Rice Industry:
N-((4-Chlorophenyl)methyl)-N-cyclopentyl-N'-phenylurea is used as a fungicide for controlling sheath blight in rice. This application helps in protecting the rice crop from the damaging effects of the sheath blight disease, ensuring better crop health and increased productivity.
Used in Cotton Industry:
N-((4-Chlorophenyl)methyl)-N-cyclopentyl-N'-phenylurea is used as a fungicide for controlling diseases caused by Rhizoctonia solani and Pellicularia spp. in cotton. This application aids in maintaining the health of the cotton crop and reducing the impact of these diseases on the overall yield and quality of the cotton.
Used in Sugar Beet Industry:
N-((4-Chlorophenyl)methyl)-N-cyclopentyl-N'-phenylurea is used as a fungicide for controlling diseases caused by Rhizoctonia solani and Pellicularia spp. in sugar beets. This application helps in protecting the sugar beet crop from the damaging effects of these diseases, ensuring better crop health and increased sugar yield.
Used in Vegetable Industry:
N-((4-Chlorophenyl)methyl)-N-cyclopentyl-N'-phenylurea is used as a fungicide for controlling diseases caused by Rhizoctonia solani and Pellicularia spp. in various vegetables. This application contributes to the overall health and productivity of the vegetable crops, reducing the impact of these diseases on the yield and quality of the vegetables.
Used in Ornamental Plant Industry:
N-((4-Chlorophenyl)methyl)-N-cyclopentyl-N'-phenylurea is used as a fungicide for controlling diseases caused by Rhizoctonia solani and Pellicularia spp. in ornamental plants. This application helps in maintaining the aesthetic appeal and health of ornamental plants, reducing the impact of these diseases on their overall appearance and growth.
Used in Turf Industry:
N-((4-Chlorophenyl)methyl)-N-cyclopentyl-N'-phenylurea is used as a fungicide for controlling diseases caused by Rhizoctonia solani and Pellicularia spp. in turf grasses. This application contributes to the overall health and appearance of the turf, reducing the impact of these diseases on the turf's quality and longevity.

Trade name

BAY? NTN-19701; BAYER? NTN-19701; MONCEREN?; NTN-19701?; PENCYCURONE?

Metabolic pathway

The metabolic profiles of pencycuron in fungus, hydrolysis, mammals, photodecomposition, plants, and soils are illustrated. Both tolerant and sensitive fungal species Rhizoctonia solani metabolize pencycuron to give cis- and trans-3-hydroxycyclopentyl pencycurons which are less active than pencycuron.

Degradation

Pencycuron is a very stable compound. Its DT50 in water at pH 4 is 280 days and at pH values 7 and 9 the estimated DT50 values are 22 and 17 years, respectively. It is photolysed in water and on soil surfaces.

Check Digit Verification of cas no

The CAS Registry Mumber 66063-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,6 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66063-05:
(7*6)+(6*6)+(5*0)+(4*6)+(3*3)+(2*0)+(1*5)=116
116 % 10 = 6
So 66063-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H21ClN2O/c20-16-12-10-15(11-13-16)14-22(18-8-4-5-9-18)19(23)21-17-6-2-1-3-7-17/h1-3,6-7,10-13,18H,4-5,8-9,14H2,(H,21,23)

66063-05-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name pencycuron

1.2 Other means of identification

Product number -
Other names 1-(4-chlorobenzyl)-1-cyclopentyl-3-phenylurea

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66063-05-6 SDS

66063-05-6Relevant academic research and scientific papers

Substituted imide derivatives

-

, (2008/06/13)

The present invention relates to novel substituted imide derivatives of the general formula (I) in which R1 represents optionally substituted cycloalkyl, R2 represents optionally substituted alkyl or optionally substituted cycloalkyl, R3 represents alkyl, alkoxy, alkylthio, amino, alkylamino or dialkylamino and R4 represents cyano or nitro, and to processes for their preparation and to their use for controlling animal pests and as herbicides.

Pyrazolyl benzyl ether derivatives containing a fluoromethoxyimino group and use thereof as pesticides

-

, (2008/06/13)

The invention relates to novel pyrazolyl benzyl ethers, to a plurality of processes for their preparation and to their use for controlling harmful organisms.

Iminoacetic acid amides and their use as pest control agents

-

, (2008/06/13)

PCT No. PCT/EP96/04345 Sec. 371 Date Apr. 15, 1998 Sec. 102(e) Date Apr. 15, 1998 PCT Filed Oct. 7, 1996 PCT Pub. No. WO97/14673 PCT Pub. Date Apr. 24, 1997Iminoacetamides of the formula (I) in which A represents a single bond or optionally substituted alkylene, Q represents oxygen or sulphur, R1 represents respectively optionally substituted cycloalkyl, cycloalkenyl, aryl or heterocyclyl, R2 represents respectively optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl or heterocyclyl, R3 represents hydrogen or respectively optionally substituted alkyl, alkenyl, alkinyl or cycloalkyl, R4 represents respectively optionally substituted cycloalkyl, cycloalkenyl, aryl or heterocyclcyl a process for their preparation, pesticidal compositions containing them, and their use for controlling pests.

2-and 2,5-substituted phenylketoenols

-

, (2008/06/13)

PCT No. PCT/EP97/03973 Sec. 371 Date Jan. 28, 1999 Sec. 102(e) Date Jan. 28, 1999 PCT Filed Jul. 23, 1997 PCT Pub. No. WO98/05638 PCT Pub. Date Feb. 12, 1998The invention relates to novel phenyl-substituted cyclic ketoenols of the formula (I) in which Het represents one of the groups in which A, B, D, G, X and Z are each as defined in the description, to a plurality of processes and intermediates for their preparation, and to their use as pesticides.

Microbicidal benzotriazoles

-

, (2008/06/13)

Novel benzotriazoles of the formula STR1 in which R, X1, X2, X3, X4 and Y have the meanings given in the description, and their acid addition salts and metal salt complexes, a process for the preparation of these substances and their use as microbicides in crop protection and in material protection.

Halogen alkenyl azolyl microbicides

-

, (2008/06/13)

Novel halogenoalkenyl-azolyl derivatives of the formula STR1 in which R1 represents optionally substituted alkyl, optionally substituted alkenyl, optionally substituted cycloalkyl, optionally substituted aryl or represents optionally substituted heteroaryl, R2 represents alkyl, halogenoalkyl, 1-hydroxyalkyl, 2-hydroxyalkyl, 1-hydroxyhalogenalkyl, 1-alkenyl or 2-alkenyl, X1 represents fluorine, chlorine, bromine or iodine, X2 represents fluorine, chlorine, bromine or iodine, and Y represents nitrogen or a CH group, and addition products thereof with acids or metal salts are very active as microbicides in plant protection and in the protection of materials.

Substituted biphenyl oxazolines

-

, (2008/06/13)

The invention relates to new substituted biphenyloxazolines of the formula (I) STR1 in which R1 represents C1 -C6 -halogenoalkylthio and R2 represents hydrogen, or R1 and R2 together with the carbon atoms to which they are bonded form a halogen-substituted 5- or 6-membered heterocyclic ring, X represents hydrogen, halogen, C1 -C6 -alkyl or C1 -C6 -alkoxy, and m represents 0, 1 or 2, to processes for their preparation, to new intermediates, and to the use of the substituted biphenyloxazolines for combating animal pests, with the exception of the compound of the formula STR2

Acylated 5-aminopyrazoles and the use thereof to combat animal parasites

-

, (2008/06/13)

The present invention relates to new acylated 5-aminopyrazoles of the formula (I) STR1 in which R1, R2, R3, R4 and R5 have the meaning given in the description, to processes for their preparation and to their use as pesticides.

Substituted tetrahydro-5-nitro-pyrimidines

-

, (2008/06/13)

The present invention relates to novel substituted in that one tetrahydro-5-nitro-pyrimidine of the formula (I), according to claim 1, STR1 in which n, R1, R2 have the meaning given in the description, to a process for its preparation and to its use for combating animal pests, especially insects, arachnids and nematodes, which are encountered in agricultural, in forestry, in the protection of stored products and of materials and, in the hygiene sector.

Fungicidal composition for seed dressing

-

, (2008/06/13)

The present invention relates to a fungicidal composition intended for the protection of the multiplication products of cultivated plants, containing: (a) 2-(4-chlorobenzylidene)-5,5-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)-1-cyclopentanol; (b) one or more fungicides suitable for the protection of the said multiplication products, optionally one or more insecticides, (c), an agriculturally acceptable inert vehicle and an agriculturally acceptable surfactant. The invention also relates to a method for protecting the multiplication products of plants against fungal diseases using these compositions.

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