17994-63-7

Basic information

• Product Name: BUTTPARK 78\40-45
• Synonyms: BUTTPARK 78\40-45;4-(2-CL-PH)-6-ME-2-OXO-1,2,3,4-4H-PYRIMIDINE-5-CARBOXYLIC ACID ETHYL ESTER;4-(2-Chloro-phenyl)-6-methyl-2-oxo-1,2,3,4-tetra-hydro-pyrimidine-5-carboxylic acid ethyl este;ethyl 4-(2-chlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
• CAS NO: 17994-63-7
• Molecular Formula: C₁₄H₁₅ClN₂O₃
• Molecular Weight: 294.73
• Mol File: 17994-63-7.mol
• Article Data: 107

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BUTTPARK 78\40-45(CAS DataBase Reference)
• NIST Chemistry Reference: BUTTPARK 78\40-45(17994-63-7)
• EPA Substance Registry System: BUTTPARK 78\40-45(17994-63-7)

Safety Data

• Hazardous Substances Data: 17994-63-7(Hazardous Substances Data)

Upstream product

• 89-98-5 2-chloro-benzaldehyde 
• 141-97-9 ethyl acetoacetate 
• 17849-38-6 2-Chlorobenzyl alcohol 
• 674-82-8 4-methyleneoxetan-2-one 
• 64-17-5 ethanol 
• 57-13-6 urea 
• 611-19-8 1-chloro-2-(chloromethyl)benzene 

Downstream Products

• 1445609-61-9 ethyl 4-(2-chlorophenyl)-6-(dichloromethyl)-1,2,3,4-tetrahydro-2-oxopyrimidine-5-carboxylate 
• 1417542-47-2 ethyl 6-methyl-2-oxo-4-(2-chlorophenyl)-3-[(4-phenyl-1H-1,2,3-triazol-1-yl)methyl]-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1448024-58-5 (E)-ethyl 4-(2-chlorophenyl)-6-methyl-2-oxo-3-(3-p-tolylallyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1448024-44-9 (E)-ethyl 4-(2-chlorophenyl)-3-cinnamyl-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1426902-87-5 ethyl 3-[({[(E)-4-chlorobenzylidene]amino}oxy)methyl]-6-methyl-2-oxo-4-(2-chlorophenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1426902-94-4 ethyl 3-[({[diphenylmethylene]amino}oxy)methyl]-6-methyl-2-oxo-4-(2-chlorophenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 302821-56-3 C₁₆H₁₇ClN₂O₄ 
• 680211-43-2 C₁₄H₁₄BrClN₂O₃ 

Relevant articles and documents

Effect of poly(ethylene glycol)-400 and carbon on MoO3 nanocomposite materials and its catalytic activity for Biginelli reactions

The effect of addition of poly(ethylene glycol)-400 (PEG-400) and carbon (0, 1, 2 and 3 wt%) as substrates were investigated systematically to get the desired phase of carbon-doped MoO3 material. The carbon source was prepared from the Acacia a

Solid state synthesis, characterization, optical properties and cooperative catalytic performance of bismuth vanadate nanocatalyst for Biginelli reactions

Bi2V2O7 nano powders were synthesized via a solid state reaction at 500°C for 8 h using Bi(NO3)3 and VO(acac)2 at stoichiometric 1:1 Bi:V molar ratio as raw materials. The synthesized mater

RETRACTED ARTICLE: Boric acid in magnetized water: Clean and powerful media for synthesis of 3,4-dihydropyrimidin-2(1: H)-ones

Water was magnetized via an external magnetic field and employed, for the first time, as a solvent in green preparation of 3,4-dihydropyrimidin-2(1H)-ones by the one-pot three-component condensation reaction using boric acid as a catalyst. Shorter reactio

Synthesis and catalytic application of D-glucose derived ytterbium(III) complex in Biginelli reaction

4,6-O-Ethylidene-N-(2-hydroxybenzylidene)-β-D-glucopyranosylamine has been reacted with ytterbium(III) acetate and the resultant complex has been used as catalyst in the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones (DHPMs). Twenty-one DHPMs have been synthesised under neat reaction condition in appreciable yields (73–96percent) and reusability of the catalyst has been established.

Synthesis and characterization of the immobilized polythiophene on magnetic carbon nanotube as a prominent catalyst for the synthesis of dihydropyrimidinone and octahydroquinazolinone derivatives

Abstract: In this work, the immobilized polythiophene on magnetic carbon nanotube (CNT–Fe3O4–PTh) was synthesized and introduced as a novel and recoverable catalytic system. The prepared magnetic heterogeneous nanocatalyst was characterized by FT-IR, TGA, EDX, VSM, XRD, TEM, and FE-SEM. Next, the catalytic efficiency of CNT–Fe3O4–PTh was evaluated through the green synthesis of a variety of dihydropyrimidinone and octahydroquinazolinone through Biginelli reaction between aromatic aldehydes, urea/thiourea, and β-dicarbonyl compounds under solvent-free conditions. The catalyst was magnetically recovered and recycled for five cycles without a discernible loss in its catalytic activity. Simple workup, affordability, short reaction times, mild reaction conditions, and the high yield of products are the interesting features of this project. Graphic abstract: An environmentally benign nanocomposite was prepared using carbon nanotube as an inexpensive, nontoxic, and stable support in the preparation of CNT–Fe3O4–PTh, which was efficiently used as catalyst for the green synthesis of dihydropyrimidinone and octahydroquinazolinone derivatives through Biginelli reaction under solvent-free conditions.[Figure not available: see fulltext.].