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5957-86-8

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5957-86-8 Usage

Physical form

Yellow crystalline solid

Common uses

Intermediate in the synthesis of pharmaceuticals and agricultural chemicals

Odor

Strong

Solubility

Insoluble in water, soluble in organic solvents

Usage in pesticides and herbicides

Disrupts the growth of unwanted plants or pests

Potential properties

Antiparasitic and anti-inflammatory

Toxicological effects

Still a subject of ongoing research

Check Digit Verification of cas no

The CAS Registry Mumber 5957-86-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5957-86:
(6*5)+(5*9)+(4*5)+(3*7)+(2*8)+(1*6)=138
138 % 10 = 8
So 5957-86-8 is a valid CAS Registry Number.

5957-86-8Downstream Products

5957-86-8Relevant articles and documents

Nickel-Catalyzed Reductive 2-Pyridination of Aryl Iodides with Difluoromethyl 2-Pyridyl Sulfone

Miao, Wenjun,Ni, Chuanfa,Xiao, Pan,Jia, Rulong,Zhang, Wei,Hu, Jinbo

supporting information, p. 711 - 715 (2021/01/26)

A novel nickel-catalyzed reductive cross-coupling between aryl iodides and difluoromethyl 2-pyridyl sulfone (2-PySO2CF2H) enables C(sp2)-C(sp2) bond formation through selective C(sp2)-S bond cleavage, which demonstrates the new reactivity of 2-PySO2CF2H reagent. This method employs readily available nickel catalyst and sulfones as cross-electrophile coupling partners, providing facile access to biaryls under mild reaction conditions without pregeneration of arylmetal reagents.

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

-

Paragraph 00514; 00515; 00516; 00582; 00583; 00584, (2019/07/17)

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with the enzyme glycolate oxidase (GO). Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

Ligand-promoted ruthenium-catalyzed: Meta C-H chlorination of arenes using N -chloro-2,10-camphorsultam

Fan, Zhoulong,Lu, Heng,Cheng, Zhen,Zhang, Ao

supporting information, p. 6008 - 6011 (2018/06/18)

A practical meta C-H chlorination protocol is established via a Ru(0)-catalyzed ortho-metalation strategy. The use of N-chloro-2,10-camphorsultam as a new chlorinating agent is crucial for the success of the current reaction and an N-heterocyclic carbene (NHC) ligand could significantly enhance the reactivity of the catalytic transformation. The mechanistic studies reveal that an unusual ortho C-H ruthenation relay process with ortho chlorination of the C-Ru bond is probably involved.

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