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Tembotrione [iso], also known as 2-benzoylcyclohexane-1,3-dione, is an aromatic ketone herbicide characterized by its unique structure with chlorine, (2,2,2-trifluoroethoxy)methyl, and methylsulfonyl groups at positions 2, 3, and 4 of the phenyl group. It is specifically designed for post-emergence application and is used in conjunction with the herbicide safener cyprosulfamide.

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  • 335104-84-2 Structure
  • Basic information

    1. Product Name: Tembotrione [iso]
    2. Synonyms: Tembotrione;Tembotrione [iso];2-[2-Chloro-4-(methylsulfonyl)-3-[(2,2,2-trifluoroethoxy)methyl]benzoyl]-1,3-cyclohexanedione;BAY 747;2-{2-chloro-4-(methylsulfonyl)-3-[(2,2,2-trifluoroethoxy)methyl]benzoyl}cyclohexane-1,3-dione;TEMBOTRIONE(WXC06044)
    3. CAS NO:335104-84-2
    4. Molecular Formula: C17H16ClF3O6S
    5. Molecular Weight: 440.8185496
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 335104-84-2.mol
    9. Article Data: 7
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 612.86°C at 760 mmHg
    3. Flash Point: 324.446°C
    4. Appearance: /
    5. Density: 1.458g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.519
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 3.17±0.50(Predicted)
    11. CAS DataBase Reference: Tembotrione [iso](CAS DataBase Reference)
    12. NIST Chemistry Reference: Tembotrione [iso](335104-84-2)
    13. EPA Substance Registry System: Tembotrione [iso](335104-84-2)
  • Safety Data

    1. Hazard Codes: Xn,N
    2. Statements: 43-50/53
    3. Safety Statements: 36/37-60-61
    4. RIDADR: UN 3077 9 / PGIII
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 335104-84-2(Hazardous Substances Data)

335104-84-2 Usage

Uses

Used in Agricultural Industry:
Tembotrione [iso] is used as a post-emergence herbicide for the control of a wide range of broad-leaved and grassy weeds in corn and other crops. Its application helps to protect and maintain the health of these crops by reducing the competition from weeds, which can negatively impact crop yield and quality.
In addition to its primary use in agriculture, Tembotrione [iso] may also have potential applications in other industries, such as:
Used in Environmental Management:
Tembotrione [iso] can be employed as a tool for environmental management, particularly in the control of invasive plant species that can disrupt ecosystems and cause harm to native flora and fauna. By targeting and controlling these invasive species, Tembotrione [iso] can contribute to the preservation of biodiversity and the overall health of ecosystems.
Used in Research and Development:
As a chemical compound with unique properties, Tembotrione [iso] may also be utilized in research and development for the creation of new herbicides or other agrochemical products. Its study can lead to a better understanding of its mode of action, potential synergistic effects with other compounds, and the development of more effective and targeted weed control solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 335104-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,1,0 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 335104-84:
(8*3)+(7*3)+(6*5)+(5*1)+(4*0)+(3*4)+(2*8)+(1*4)=112
112 % 10 = 2
So 335104-84-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H16ClF3O6S/c1-28(25,26)13-6-5-9(15(18)10(13)7-27-8-17(19,20)21)16(24)14-11(22)3-2-4-12(14)23/h5-6,14H,2-4,7-8H2,1H3

335104-84-2 Well-known Company Product Price

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  • Sigma-Aldrich

  • (32766)  Tembotrione  PESTANAL®, analytical standard

  • 335104-84-2

  • 32766-100MG

  • 780.39CNY

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335104-84-2Downstream Products

335104-84-2Relevant articles and documents

Method for preparing triketone compound through continuous flow

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Paragraph 0029-0031, (2021/09/08)

The invention relates to a method for preparing a triketone compound through continuous flow, which uses substrate acyl chloride and 1, 3 - cyclohexanedione as a raw material and is subjected to esterification. The method is mild in condition, simple to operate, good in stability and high in reliability. Utilize continuous flow can accurate control dwell time, the good characteristics of mass transfer heat transfer, easily realize accurate control, restrain the production of side reaction, and reaction yield is high. The method has remarkable innovation meaning and economic value, is easy for industrialization and has a wide prospect.

Purification method of tembotrions product

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Paragraph 0052-0055, (2020/08/02)

The invention relates to a purification method of a tembotrions product. The method comprises the following steps: 1) dissolving the tembotrions product in an aqueous solution, and heating; 2) addingan adsorbent, and carrying out heat preservation and hot filtration; and 3) controlling the temperature, adjusting the pH value of the aqueous solution to be less than 3, cooling, and crystallizing purified tembotrions from the solution. According to the purification method of the sulfadione product, the content of cyanide impurities in the sulfadione product can be greatly reduced, the purity ofthe product is improved, and the content of the cyanide impurities is reduced from 1327 ppm to 100 ppm or below by performing Ames detection on the tembotrions product before purification and the purified product.

Synthetic process of herbicide tembotrione

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Paragraph 0036; 0044; 0045; 0046; 0047; 0055; 0056; 0057, (2019/05/08)

The invention discloses a synthetic process of herbicide tembotrione. The synthetic process comprises the following steps: step 1) adding methyl 2-chloro-3-methyl-4-methylsulfonylbenzoate, a solvent,a catalyst and hydrobromic acid at the first, then dropwise adding hydrogen peroxide, washing with water, concentrating and recrystallizing after reaction to obtain bromine methyl 2-chloro-3-bromomethyl-4-methylsulfonylbenzoate; step 2) enabling the bromide, an alkali 1, the catalyst, the solvent and 2,2,2-trifluoroethanol to react, filtering, washing with water and concentrating after reaction; adding an alkali 2 and water to react, acidifying, filtering, washing and drying to obtain an etherate 2-chloro-3-(2,2,2-trifluoroethoxy)methyl-4-methanesulfonylbenzoic acid; and step 3) removing the solvent after reacting the etherate, the catalyst, thionyl chloride and the solvent; adding 1,3-cyclohexanedione and the solvent, dropwise adding triethylamine; adding acetone cyanohydrin after reaction, washing with water, layering, removing the solvent from an oil layer, adding the solvent for recrystallization, filtering and drying to obtain a beige solid, namely tembotrione. The synthetic process provided by the invention increases the yield of an intermediate, is more environmentally-friendly and safer, and reduces production costs.

NOXIOUS ARTHROPOD CONTROL AGENT CONTAINING AMIDE COMPOUND

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, (2017/08/26)

An object of the present invention is to provide a compound having the controlling activity on a noxious arthropod, and a noxious arthropod controlling agent containing an amide compound of formula (I): wherein X represents a nitrogen atom or a CH group, p represents 0 or 1, A represents a tetrahydrofuranyl group or the like, R1, R2, R3, R4, R5, R6 and R7 represent a hydrogen atom or the like, n represents 1 or 2, Y represents an oxygen atom or the like, m represents any integer of 0 to 7, and Q represents a C1-8 chain hydrocarbon group optionally having a phenyl group or the like, has the excellent noxious arthropod controlling effect.

Process for synthesis of Triketone-based herbicide link sulphur grass alkone

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, (2016/11/24)

The invention relates to a process for synthesizing triketone herbicide cyclic sulcotrione. The method comprises the following steps: (1) synthesizing 2-chloro-6-methylsulfonyl methylbenzene; (2) synthesizing 2-chloro-3-acetyl-6-methylsulfonyl methylbenzene; (3) synthesizing 2-chloro-3-methyl-4-methylsulfonyl benzoic acid; (4) synthesizing methyl 2-chloro-3-methyl-4-methylsulfonyl benzoate; (5) synthesizing methyl 2-chloro-3-bromomethyl-4-methylsulfonyl benzoate; (6) synthesizing 2-chloro-3-(2,2,2-trifluoroethyoxy)methyl-4-methylsulfonyl benzoic acid; (7) synthesizing 2-chloro-3-(2,2,2-trifluoroethyoxy)methyl-4-methylsulfonyl benzoic acid 3-oxo-1-cyclohexene ester; and (8) synthesizing cyclic sulcotrione. The process disclosed by the invention has the beneficial effects that the reaction steps are reduced, the reaction time is shortened, and the yield of intermediates is improved; the reaction conditions are mild and safe; and the cost is reduced.

HERBICIDAL COMPOSITION

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Page/Page column 12, (2010/08/08)

To provide a herbicidal composition and a method for its application, whereby the effect of a herbicidally active ingredient is improved to reduce the environmental load on a site where the herbicide is applied or the periphery thereof, more than ever, and its dose can be reduced. A herbicidal composition comprising (1) a compound represented by the formula (I) or its salt: where T and Z are as defined in the specification, and (2) a polyoxyalkylene alkyl ether phosphate or its salt. A method for controlling undesired plants or inhibiting their growth, by applying the herbicidal composition.

Herbicidal mixture comprising a benzoyl derivative, a fertilizer containing nitrogen and an adjuvant.

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, (2008/06/13)

Herbicidal mixture comprising a benzoyl derivative, a fertilizer containing nitrogen and an adjuvant. A method of controlling the growth of weeds at a locus which comprises applying to said locus a herbicidally effective amount of: (a) a benzoyl derivative of formula (I): 1wherein R1, R2, R3, R4, R5 and w are as defined in the description; (b) a fertilizer containing nitrogen; and (c) one or more adjuvants; and to their compositions thereof.

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