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BENZENEACETIC ACID, 3,5-DICHLORO-, ETHYL ESTER is a chemical compound with the molecular formula C10H9Cl2O2. It is an ethyl ester of 3,5-dichlorobenzoic acid, characterized by its colorless to pale yellow liquid appearance and a strong, sweet, and fruity odor. BENZENEACETIC ACID, 3,5-DICHLORO-, ETHYL ESTER is widely recognized for its role as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, and it requires careful handling due to its potential health hazards such as skin and eye irritation and respiratory issues upon inhalation.

200214-60-4

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200214-60-4 Usage

Uses

Used in Pharmaceutical Industry:
BENZENEACETIC ACID, 3,5-DICHLORO-, ETHYL ESTER is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, BENZENEACETIC ACID, 3,5-DICHLORO-, ETHYL ESTER serves as an essential intermediate in the production of agrochemicals, including pesticides and herbicides, due to its reactive chemical structure that can be modified to target specific pests or weeds.
Used in Chemical Synthesis:
BENZENEACETIC ACID, 3,5-DICHLORO-, ETHYL ESTER is utilized as an intermediate in the synthesis of a range of chemical products, highlighting its versatility in organic chemistry and its potential applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 200214-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,2,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 200214-60:
(8*2)+(7*0)+(6*0)+(5*2)+(4*1)+(3*4)+(2*6)+(1*0)=54
54 % 10 = 4
So 200214-60-4 is a valid CAS Registry Number.

200214-60-4Downstream Products

200214-60-4Relevant academic research and scientific papers

Synthesis of α-aryl esters and nitriles: Deaminative coupling of α-aminoesters and α-aminoacetonitriles with arylboronic acids

Wu, Guojiao,Deng, Yifan,Wu, Chaoqiang,Zhang, Yan,Wang, Jianbo

supporting information, p. 10510 - 10514 (2016/02/18)

Transition-metal-free synthesis of α-aryl esters and nitriles using arylboronic acids with α-aminoesters and α-aminoacetonitriles, respectively, as the starting materials has been developed. The reaction represents a rare case of converting C(sp3)-N bonds into C(sp3)-C(sp2) bonds. The reaction conditions are mild, demonstrate good functional-group tolerance, and can be scaled up. Touch base: A transition-metal-free protocol for the synthesis of α-aryl esters and nitriles by deaminative coupling is presented. Strong bases and transition-metal catalysts are not needed. The new synthetic method uses readily available starting materials and demonstrates wide substrate scope.

1-HETEROCYCLYL-1,5-DIHYDRO-PYRAZOLO[3,4-D] PYRIMIDIN-4-ONE DERIVATIVES AND THEIR USE AS PDE9A MODULATORS

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Page/Page column 163-164, (2009/10/30)

The invention relates to novel 1,6-disubstituted pyrazolopyrimidinones, Formula (I) with Hc is a mono-, bi- or tricyclic heterocyclyl group, the ring members of which are carbon atoms and at least 1, preferably 1, 2 or 3, heteroatom(s), which are selected from the group of nitrogen, oxygen and sulphur, which is in the form of -S(O)r - with r being 0, 1 or 2, and - said heterocyclyl group is or comprises 1 non-aromatic, saturated, or partly unsaturated monocyclic ring which comprises at least 1 heteroatom as ring member and - said heterocyclyl group is bound to the scaffold by said 1 non- aromatic, saturated, or partly unsaturated monocyclic ring which comprises at least 1 heteroatom as ring member. According to one aspect of the invention the new compounds are for the manufacture of medicaments, in particular medicaments for the treatment of conditions concerning deficits in perception, concentration, learning or memory. The new compounds are also for the manufacture of medicaments for the treatment of Alzheimer's disease.

AMINO ACID DERIVATIVES AND THEIR USE AS THROMBIN INHIBITORS

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, (2008/06/13)

There is provided compounds of formula I, wherein R 1, R 2, R 3, R x, Y, n and B have meanings given in the description which are useful as competitive inhibitors of trypsin-like proteases, such as thrombin, and in particular in the treatment of conditions where inhibition of thrombin is required as in thrombosis or as anticoagulants.

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