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ETHYL 4-ETHOXY-2-PHENYL-5-PYRIMIDINECARBOXYLATE is a chemical compound characterized by the molecular formula C16H16N2O3. It is an ethyl ester derivative of pyrimidinecarboxylic acid, featuring a phenyl group at the 2nd position and an ethoxy substituent at the 4th position. ETHYL 4-ETHOXY-2-PHENYL-5-PYRIMIDINECARBOXYLATE exhibits a white to light yellow color and is widely recognized for its utility in the pharmaceutical and agrochemical sectors, primarily as a building block for the synthesis of a variety of drugs and pesticides. The distinctive structural attributes and functional groups of ETHYL 4-ETHOXY-2-PHENYL-5-PYRIMIDINECARBOXYLATE render it a highly adaptable intermediate in organic synthesis, with broad implications in medicinal chemistry and crop protection.

122773-99-3

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122773-99-3 Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 4-ETHOXY-2-PHENYL-5-PYRIMIDINECARBOXYLATE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of novel drug molecules. Its unique structure allows for the creation of compounds with potential therapeutic properties, making it valuable in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, ETHYL 4-ETHOXY-2-PHENYL-5-PYRIMIDINECARBOXYLATE is utilized as a building block for the synthesis of pesticides. Its incorporation into these products can enhance their effectiveness in crop protection, contributing to the development of more efficient and targeted pest control agents.
Used in Organic Synthesis:
ETHYL 4-ETHOXY-2-PHENYL-5-PYRIMIDINECARBOXYLATE is employed as a versatile intermediate in organic synthesis due to its capacity to react with various reagents and participate in multiple types of chemical reactions. This adaptability makes it a valuable component in the creation of a wide array of organic compounds for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 122773-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,7,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122773-99:
(8*1)+(7*2)+(6*2)+(5*7)+(4*7)+(3*3)+(2*9)+(1*9)=133
133 % 10 = 3
So 122773-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H16N2O3/c1-3-19-14-12(15(18)20-4-2)10-16-13(17-14)11-8-6-5-7-9-11/h5-10H,3-4H2,1-2H3

122773-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-ethoxy-2-phenylpyrimidine-5-carboxylate

1.2 Other means of identification

Product number -
Other names 4-Aethoxy-2-phenyl-pyrimidin-5-carbonsaeure-aethylester

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:122773-99-3 SDS

122773-99-3Downstream Products

122773-99-3Relevant academic research and scientific papers

Thiono and dithio estes, LII: Reaction of dithiono malonates with N,N-dimethylformamide acetals

Hartke,Kraska

, p. 57 - 60 (2007/10/02)

The reaction of the dithiono malonates 1 with the formamide acetals 2 leads to the 2-dialkylaminomethylene dithionomalonates 4 and the thiono acrylates 6. The condensation of 4 with hydrazines gives rise to the pyrazoles 7 and 8, with hydroxylamine sulfon

SYNTHESIS OF 2,5'-BIPYRIMIDINES FROM SUBSTITUTED 5-CYANOPYRIMIDINES

Mamaev, V. P.,Mikhaleva, M. A.,Shadrina, A. I.

, p. 303 - 307 (2007/10/02)

The Pinner method was applied to substituted 5-cyanopyrimidines to obtain 5-aminopyrimidines, which were condensed with acrolein derivatives to synthesize compounds that contain a 2,5-bipyrimidine fragment.

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