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Benzenepropanoic acid, 2-chloro-b-hydroxy-a-methylene-, ethyl ester, also known as clofibrate, is a synthetic chemical compound belonging to the class of fibrates. It is an ethyl ester derivative of benzenepropanoic acid, featuring a 2-chloro-b-hydroxy-a-methylene group. Clofibrate is primarily used as a lipid-lowering agent in the treatment of hyperlipidemia, a condition characterized by elevated levels of lipids in the blood. It functions by activating peroxisome proliferator-activated receptors (PPARs), which in turn increase the breakdown of fats and reduce their levels in the blood. The compound has a molecular formula of C11H15ClO3 and a molecular weight of 230.69 g/mol. Clofibrate is an odorless, white crystalline powder that is insoluble in water but soluble in organic solvents. It is typically administered orally and has been used to manage conditions such as atherosclerosis, coronary heart disease, and pancreatitis associated with high lipid levels. However, its use has been limited due to potential side effects and the availability of alternative medications with fewer risks.

88039-46-7

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88039-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88039-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,3 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88039-46:
(7*8)+(6*8)+(5*0)+(4*3)+(3*9)+(2*4)+(1*6)=157
157 % 10 = 7
So 88039-46-7 is a valid CAS Registry Number.

88039-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-((2-chlorophenyl)(hydroxy)methyl)acrylate

1.2 Other means of identification

Product number -
Other names 2-[hydroxy(2-chlorophenyl)methyl]acrylic 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:88039-46-7 SDS

88039-46-7Relevant academic research and scientific papers

Silver/palladium relay catalyzed 1,3-dipole annulation/allylation reactions to access fully substituted allyl imidazolidines

Han, Ruiping,Ding, Yue,Jin, Xueke,Li, Er-Qing

supporting information, p. 646 - 649 (2020/02/11)

A silver/palladium relay catalyzed 1,3-dipole annulation/allylation reaction of iminoesters and Baylis-Hillman acetates for the construction of fully substituted allyl imidazolidines is reported. The reaction of both iminoesters and Baylis-Hillman acetate

Direct Synthesis of Dihydropyrrolo[2,1-a]Isoquinolines through FeCl3 Promoted Oxidative Aromatization

Cui, Hai-Lei,Jiang, Lu,Tan, Hao,Liu, Si

supporting information, p. 4772 - 4780 (2019/10/28)

We have developed a straightforward FeCl3 promoted synthesis of dihydropyrrolo[2,1-a]isoquinolines through formal (3+2) cycloaddition/oxidative aromatization cascade of dihydroisoquinoline with Morita-Baylis-Hillman carbonates (up to 96% yield)

Fe(III)-Catalyzed Hydroallylation of Unactivated Alkenes with Morita-Baylis-Hillman Adducts

Qi, Jifeng,Zheng, Jing,Cui, Sunliang

supporting information, p. 1355 - 1358 (2018/03/09)

An Fe(III)-catalyzed hydroallylation of unactivated alkenes with Morita-Baylis-Hillman adducts via an Fe-catalyzed process is described. A variety of alkenes, including mono-, di-, and trisubstituted alkenes, could all smoothly convert to structural diver

Methylsulfenylation of Electrophilic Carbon Atoms: Reaction Development, Scope, and Mechanism

Pereira, Adriane A.,Pereira, Amanda S.,de Mello, Amanda C.,Carpanez, Arthur G.,Horta, Bruno A. C.,Amarante, Giovanni W.

supporting information, p. 1578 - 1582 (2017/04/06)

An innovative method for the methylsulfenylation of electrophilic carbons was explored. Cheap and commercially available dimethyl sulfoxide (DMSO) was used as a source of the –SCH3 group. Chalcone, dibenzylideneacetone, and Morita–Baylis–Hillma

Catalytic Enantioselective Vinylogous Allylic Alkylation of Coumarins

Kayal, Satavisha,Mukherjee, Santanu

supporting information, p. 4944 - 4947 (2017/09/23)

An unprecedented, organocatalytic enantioselective vinylogous γ-allylic alkylation of 4-methylcoumarins has been developed. Using allylic carbonates as the allyl source, this reaction is catalyzed by Lewis basic dimeric Cinchona alkaloid (QD)2P

Electrophilic warhead-based design of compounds preventing NLRP3 inflammasome-dependent pyroptosis

Cocco, Mattia,Garella, Davide,Di Stilo, Antonella,Borretto, Emily,Stevanato, Livio,Giorgis, Marta,Marini, Elisabetta,Fantozzi, Roberto,Miglio, Gianluca,Bertinaria, Massimo

, p. 10366 - 10382 (2015/02/19)

Pyroptosis is a caspase-1-dependent pro-inflammatory form of programmed cell death implicated in the pathogenesis of autoinflammatory diseases as well as in disorders characterized by excessive cell death and inflammation. Activation of NLRP3 inflammasome

PYRIDOPYRIMIDINE BASED DERIVATIVES AS POTENTIAL PHOSPHODIESTERASE 3 (PDE3) INHIBITORS AND A PROCESS FOR THE PREPARATION THEREOF

-

Paragraph 0082; 0083; 0084; 0090, (2014/08/19)

The present invention provides compounds of formula 1 as potential phosphodiesterase3 (PDE3) inhibitory agents and a process for the preparation thereof. The derivatives of formula 1 can be employed as therapeutics in human and veterinary medicine, where

INDOLIZINONE BASED DERIVATIVES AS POTENTIAL PHOSPHODIESTERASE 3 (PDE3) INHIBITORS AND A PROCESS FOR THE PREPARATION THEREOF

-

Paragraph 0060, (2014/10/16)

The present invention provides compounds of general formula A useful as potential phosphodiesterase3 (PDE3) inhibitory agents and a process for the preparation thereof. The derivatives of formula A can be employed as therapeutics in human and veterinary medicine, where they can be used, for example, for the treatment and prophylaxis of the following diseases: heart failure, dilated cardiomyopathy, platelet inhibitors, cancer and obstructive pulmonary diseases.

Synthesis and evaluation of novel 2-pyridone derivatives as inhibitors of phosphodiesterase3 (PDE3): A target for heart failure and platelet aggregation

Ravinder, Mettu,Mahendar, Budde,Mattapally, Saidulu,Hamsini, Kommi Venkata,Reddy, Thatikonda Narendar,Rohit, Chilappa,Srinivas, Kolupula,Banerjee, Sanjay Kumar,Rao, Vaidya Jayathirtha

, p. 6010 - 6015 (2012/11/07)

Twenty-six 2-pyridone derivatives (8a-8z), which are structurally analogous to amrinone and milrinone two important cardiotonic drugs, are synthesized and characterized. The synthesis of 2-pyridone derivatives involves addition, followed by cyclization be

Asymmetric synthesis of 2-alkyl-3-phosphonopropanoic acid derivatives via Rh-catalyzed asymmetric hydrogenation

Luo, Li-Bin,Wang, Dao-Yong,Zhou, Xiao-Mao,Zheng, Zhuo,Hu, Xiang-Ping

experimental part, p. 2117 - 2123 (2012/03/27)

The commercially available ferrocene-based diphosphine ligand (S c,SFc)-TaniaPhos was found to be highly effective in the Rh-catalyzed asymmetric hydrogenation of 3-aryl-2-(phosphonomethyl)propenates. Excellent enantioselectivity (90

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