Welcome to LookChem.com Sign In|Join Free
  • or
Ethyl 2-acetyl-5-oxo-3,5-diphenylpentanoate is a complex organic chemical compound with the molecular formula C19H18O4. It is a derivative of pentanoic acid, featuring a diphenylpentane core structure with an acetyl group at the 2-position and a ketone group at the 5-position. ethyl 2-acetyl-5-oxo-3,5-diphenylpentanoate is characterized by its ester linkage with an ethyl group at the 5-oxo position, which contributes to its reactivity and potential applications in organic synthesis. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural features and reactivity. The compound's properties, such as its solubility and stability, make it a valuable building block in the development of new molecules with specific therapeutic or pesticidal activities.

6265-29-8

Post Buying Request

6265-29-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6265-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6265-29-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6265-29:
(6*6)+(5*2)+(4*6)+(3*5)+(2*2)+(1*9)=98
98 % 10 = 8
So 6265-29-8 is a valid CAS Registry Number.

6265-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-acetyl-5-oxo-3,5-diphenylpentanoate

1.2 Other means of identification

Product number -
Other names 2-acetyl-5-oxo-3,5-diphenyl-valeric acid ethyl ester

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:6265-29-8 SDS

6265-29-8Downstream Products

6265-29-8Relevant academic research and scientific papers

Reaction between Chalcones, 1,3-Dicarbonyl Compounds, and Elemental Sulfur: A One-Pot Three-Component Synthesis of Substituted Thiophenes

Adib, Mehdi,Rajai-Daryasarei, Saideh,Pashazadeh, Rahim,Jahani, Mehdi,Amanlou, Massoud

, p. 1583 - 1588 (2018/06/11)

A simple and atom-economic synthesis of highly substituted thiophenes is demonstrated. Heating a solution of a chalcone and a linear/cyclic 1,3-dicarbonyl compound with elemental sulfur in CH 3 CN in the presence of NEt 3 at 80 °C af

Aminopropylated PEG as a novel, eco-friendly and biodegradable basic catalyst for bis-Michael addition to α,β-unsaturated ketones under solvent-free conditions

Khan, Tabassum,Siddiqui, Zeba N.

, p. 620 - 630 (2014/08/05)

A solvent-free and highly efficient protocol has been developed for the synthesis of novel bis-Michael addition products (3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, 3k, 3l, 3m, 3n, 3o) using aminopropylated PEG-6000 (NH 2-PEG) as a biodegradable a

Novel and versatile solid superbases derived from magnesium-zirconium composite oxide and their catalytic applications

Zhao, Jin,Xie, Jun,Au, Chak-Tong,Yin, Shuang-Feng

, p. 6159 - 6164 (2014/01/23)

Versatile solid superbases were derived from magnesium-zirconium composite oxide and KOH through thermal treatment in a N2 flow. The magnesium-zirconium composite oxide was prepared by a modified co-precipitation technique with reflux-digestion in basic solution and then mixed with KOH through grinding. The as-prepared solid superbases were characterized by low-temperature N2 physisorption, powder X-ray diffraction, and Fourier transformation infrared spectrophotometry. The superbasic sites were characterized by the use of Hammett indicators and CO2 temperature-programmed desorption methods. We found that there are ample superbasic sites (0.590 mmol g-1) on the surface with strength in the 26.5 ≤ H- 33.0 range. The as-prepared solid superbase catalyst was found to show excellent catalytic activity towards Knoevenagel condensation, Michael addition and transesterification reactions. The findings open up a new route for the synthesis of new functional superbases using composite oxides prepared by reflux-digestion in basic solution as supports.

Iron-catalyzed Michael reactions revisited: A synthetically useful process for the preparation of tri-carbonyl compounds and chiral warfarin

Yang, Hua-Meng,Gao, Yue-Hua,Li, Li,Jiang, Zhen-Yu,Lai, Guo-Qiao,Xia, Chun-Gu,Xu, Li-Wen

supporting information; experimental part, p. 3836 - 3839 (2010/08/20)

The LBAs (Lewis acid-assisted Br?nsted acid catalysis) is proposed as possible mechanistic process in the simple FeCl3-catalyzed Michael reactions of chalcones with active methylene compounds in organic solvents. And iron salts were found to be effective promoters in the asymmetric Michael addition of 4-hydroxycoumarin to α,β-unsaturated ketone, which resulted in excellent yield and high level of enantioselectivity (up to 91% ee) in the presence of low catalytic amount of iron and simple chiral primary amine.

Polyaniline-Anchored Metal Salts for Michael Reaction of ,-Unsaturated Ketones

Patel, Arun L.,Talele, Harish R.,Rama,Bedekar, Ashutosh V.

scheme or table, p. 3016 - 3023 (2009/12/01)

A catalyst consisting of polyaniline-anchored metal salts is used as a Lewis acid to promote the Michael reaction of ,-unsaturated ketones. The reaction is performed efficiently with imidazole, acetyl acetone, and ethyl acetate as Michel donors and chalcones as the acceptors under ultrasound irradiation.

Michael additions of methylene active compounds to chalcone in ionic liquids without any catalyst: The peculiar properties of ionic liquids

Meciarova, Maria,Toma, Stefan

, p. 1268 - 1272 (2007/10/03)

Michael additions of malonodinitrile as well as several other reagents to chalcone have been found to proceed well in pure ionic liquids, without the addition of any catalyst. The catalytic effect of the residual acidity caused by hydrolysis of ionic liqu

Layered double hydroxides-supported diisopropylamide: Synthesis, characterization and application in organic reactions

Kantam, M. Lakshmi,Ravindra,Reddy, Ch. Venkat,Sreedhar,Choudary

, p. 569 - 578 (2007/10/03)

The layered double hydroxides-supported diisopropylamide (LDH-DA) catalyst is found to be an efficient and selective solid base for aldol, Knoevenagel, Henry, Michael, transesterification and epoxidation reactions under liquid phase conditions. LDH-DA is synthesized by the interaction of lithium diisopropylamide with LDH-NO3 (as-synthesized) and calcined LDH-NO3. The LDH-DA (Mg/Al, 3/1) and their precursors are well characterized by using various instrumental techniques such as FT-IR, TGA and DTA, powder XRD, solid state 27Al MAS NMR spectroscopy, SEM and XPS (ESCA).

Magnesium-lanthanum mixed metal oxide: A strong solid base for the michael addition reaction

Veldurthy, Bhaskar,Clacens, Jean Marc,Figueras, Francois

, p. 767 - 771 (2007/10/03)

Michael additions were achieved quantitatively at room temperature with a broad spectrum of acceptors and donors, using a magnesium-lanthanum mixed oxide, a strong solid base. The best solvent for the reaction is dimethylformamide, but good yields were al

High surface area MgO as a highly effective heterogeneous base catalyst for michael addition and knoevenagel condensation reactions

Xu, Chunli,Bartley, Jonathan K.,Enache, Dan I.,Knight, David W.,Hutchings, Graham J.

, p. 3468 - 3476 (2007/10/03)

Magnesium oxide (MgO), obtained using a novel but simple procedure, was systematically investigated as a heterogeneous base catalyst for reactions taking place in the liquid phase, specifically the Michael addition and the Knoevenagel condensation. The ac

A rapid one-pot synthesis of 2,4,6-triaryl-3-aroyl-4-hydroxy-1,1-cyclohexanedicarbonitriles and 2-aminoisophthalonitriles under microwave activation

Laskar, Dhrubojyoti D.,Prajapati, Dipak,Sandhu, Jagir S.

, p. 135 - 139 (2007/10/03)

Ylidenemalononitriles 1 react with a variety of 1,3-diaryl-2-propen-1-ones 2 at ambient temperature and pressure under microwave activation to yield functionalised cyclohexanedicarbonitriles 3 and 2-aminoisophthalonitriles 4 in good yields.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6265-29-8