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2,4,6-Trichlorophenyl formate is a chemical compound with the molecular formula C7H3Cl3O2, typically used in industry as a pesticide, insecticide, or herbicide. It is a colorless liquid known for its toxicity, which necessitates careful handling to prevent harm to humans or the environment.

4525-65-9

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4525-65-9 Usage

Uses

Used in Pesticide Industry:
2,4,6-Trichlorophenyl formate is used as an active ingredient in pesticides for controlling pests and insects in agricultural settings. Its application is aimed at protecting crops from damage caused by these organisms, thereby ensuring a stable food supply.
Used in Insecticide Industry:
In the insecticide industry, 2,4,6-Trichlorophenyl formate is used as a potent insecticide to eliminate insects that can be harmful to humans or animals. Its application is intended to reduce the spread of diseases and maintain a healthy living environment.
Used in Herbicide Industry:
2,4,6-Trichlorophenyl formate is employed as a herbicide to control the growth of unwanted plants and weeds in various settings, such as agricultural fields, gardens, and lawns. Its application is aimed at promoting the growth of desired plants and maintaining a visually appealing landscape.

Check Digit Verification of cas no

The CAS Registry Mumber 4525-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,2 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4525-65:
(6*4)+(5*5)+(4*2)+(3*5)+(2*6)+(1*5)=89
89 % 10 = 9
So 4525-65-9 is a valid CAS Registry Number.

4525-65-9 Well-known Company Product Price

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  • TCI America

  • (T3121)  2,4,6-Trichlorophenyl Formate  >97.0%(HPLC)

  • 4525-65-9

  • 1g

  • 280.00CNY

  • Detail
  • TCI America

  • (T3121)  2,4,6-Trichlorophenyl Formate  >97.0%(HPLC)

  • 4525-65-9

  • 5g

  • 690.00CNY

  • Detail

4525-65-9Relevant academic research and scientific papers

PYRIDINONE DICARBOXAMIDE FOR USE AS BROMODOMAIN INHIBITORS

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Page/Page column 76, (2017/03/21)

The present invention relates to compounds of formula (I) and salts thereof, pharmaceutical compositions containing such compounds and to their use in therapy.

PYRIDINONE DICARBOXAMIDE FOR USE AS BROMODOMAIN INHIBITORS

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Page/Page column 53, (2017/04/11)

The present invention relates to compounds of formula (I) and salts thereof, pharmaceutical compositions containing such compounds and to their use in therapy.

2-OXO-1,2-DIHYDROPYRIDINE-3,5-DICARBOXAMIDE COMPOUNDS AS BROMODOMAIN INHIBITORS

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Page/Page column 44; 45, (2017/07/29)

The present invention relates to compounds of formula (I) and salts thereof, pharmaceutical compositions containing such compounds and to their use in therapy

Palladium-Catalyzed Carbonylative Synthesis of Aryl Formates under Mild Conditions

Jiang, Li-Bing,Li, Rui,Li, Hao-Peng,Qi, Xinxin,Wu, Xiao-Feng

, p. 1788 - 1791 (2016/06/01)

Aryl formates have been extensively applied as CO sources in CO-free carbonylation reactions. However, there are no catalytic synthetic procedures for their preparation. In this manuscript, we developed a convenient palladium-catalyzed procedure for the synthesis of aryl formates. Good yields were achieved under mild reaction conditions with formic acid as the formyl source. A formyl meeting: A convenient palladium-catalyzed carbonylation procedure for the synthesis of aryl formates is developed. Good yields are achieved under mild reaction conditions with formic acid as the formyl source.

Trichlorophenyl formate: Highly reactive and easily accessible crystalline CO surrogate for palladium-catalyzed carbonylation of aryl/alkenyl halides and triflates

Ueda, Tsuyoshi,Konishi, Hideyuki,Manabe, Kei

supporting information, p. 5370 - 5373,4 (2012/12/12)

The high utility of 2,4,6-trichlorophenyl formate, a highly reactive and easily accessible crystalline CO surrogate, is demonstrated. The decarbonylation with NEt3 to generate CO proceeded rapidly at rt, thereby allowing external-CO-free Pd-catalyzed carbonylation of aryl/alkenyl halides and triflates. The high reactivity of the CO surrogate enabled carbonylation at rt and significantly reduced the quantities of formate to near-stoichiometric levels. The obtained trichlorophenyl esters can be readily converted to a variety of carboxylic acid derivatives in high yields.

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