72509-76-3

  • Product Name:Felodipine
  • Molecular Formula:C18H19Cl2NO4
  • Purity:99%
  • Molecular Weight:384.259
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Product Details;

CasNo: 72509-76-3

Molecular Formula: C18H19Cl2NO4

Appearance: White or light yellow crystalline powder

Reputable supplier selling Felodipine 72509-76-3 with stock

  • Molecular Formula:C18H19Cl2NO4
  • Molecular Weight:384.259
  • Appearance/Colour:White or light yellow crystalline powder 
  • Vapor Pressure:4.62E-09mmHg at 25°C 
  • Melting Point:142-145 °C 
  • Refractive Index:1.549 
  • Boiling Point:471.5 °C at 760 mmHg 
  • PKA:2.73±0.70(Predicted) 
  • Flash Point:239 °C 
  • PSA:64.63000 
  • Density:1.277 g/cm3 
  • LogP:4.29310 

Felodipine(Cas 72509-76-3) Usage

Manufacturing Process

Preparation of 2,3-dichlorobenzylideneacetylacetic acid-methylester.2,3-Dichlorobenzaldehyde is reacted with methyl acetoacetate in a suitable solvent in the presence of a catalytic amount of acetic acid and piperidine. Water is azeotropically separated off during the reaction. The reaction mixture is extracted in order to remove the catalysts. The solvent is evaporated and methanol is added. The product is crystallized by cooling the solution, isolated by filtration and finally washed with methanol.

Therapeutic Function

Antihypertensive

Biological Activity

L-type Ca 2+ channel blocker that is selective over N-, R-, P/Q- and T-type channels. Displays high vascular selectivity; lowers arterial blood pressure without altering cardiac contractility. Antihypertensive.

Definition

ChEBI: The mixed (methyl, ethyl) diester of 4-(2,3-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid. A calcium-channel blocker, it lowers blood pressure by reducing peripheral vascular resistance through a highly selective action on smooth m scle in arteriolar resistance vessels. It is used in the management of hypertension and angina pectoris.

Brand name

Plendil (AstraZeneca).

General Description

Felodipine, 4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid ethylmethyl ester (Plendil), is a second-generation dihydropyridinechannel blocker of the nifedipine type. It is more selectivefor vascular smooth muscle than for myocardial tissueand serves as an effective vasodilator.

InChI:InChI=1/C18H19Cl2NO4/c1-5-25-18(23)14-10(3)21-9(2)13(17(22)24-4)15(14)11-7-6-8-12(19)16(11)20/h6-8,15,21H,5H2,1-4H3

72509-76-3 Relevant articles

An improved synthesis of high-purity felodipine

Yiu, Sai-Hay,Knaus, Edward E.

, p. 91 - 95 (1996)

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METHODS FOR TREATING CHRONIC FATIGUE SYNDROME AND MYALGIC ENCEPHALOMYELITIS

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, (2021/03/13)

In one aspect the invention relates to a...

Preparation method for felodipine

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Paragraph 0014; 0040-0042; 0045-0048; 0051-0053, (2018/12/13)

The invention discloses a preparation me...

An efficient and recyclable 3D printed α-Al2O3 catalyst for the multicomponent assembly of bioactive heterocycles

Azuaje, Jhonny,Tubío, Carmen R.,Escalante, Luz,Gómez, Mónica,Guitián, Francisco,Coelho, Alberto,Caama?o, Olga,Gil, Alvaro,Sotelo, Eddy

, p. 203 - 210 (2016/12/09)

A catalytic methodology is reported that...

Metal-free-mediated oxidation aromatization of 1,4-dihydropyridines to pyridines using visible light and air

Wei, Xiaojing,Wang, Lin,Jia, Wenliang,Du, Shaofu,Wu, Lizhu,Liu, Qiang

supporting information, p. 1245 - 1250 (2015/02/05)

A metal-free and environmentally friendl...

72509-76-3 Process route

ethyl 3-aminobut-2-enoate
626-34-6

ethyl 3-aminobut-2-enoate

acetoacetic acid methyl ester
105-45-3

acetoacetic acid methyl ester

2,3-dichlorobenzylaldehyde
6334-18-5

2,3-dichlorobenzylaldehyde

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate
72509-76-3,86189-69-7

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

Conditions
Conditions Yield
ethyl 3-aminobut-2-enoate; acetoacetic acid methyl ester; 2,3-dichlorobenzylaldehyde; With piperidine; pyridine; In neat (no solvent); at 75 - 80 ℃; for 9h;
With ethanol; for 1h; Reagent/catalyst; Solvent; Reflux;
94.3%
ethyl aminocrotonate

ethyl aminocrotonate

acetoacetic acid methyl ester
105-45-3

acetoacetic acid methyl ester

2,3-dichlorobenzylaldehyde
6334-18-5

2,3-dichlorobenzylaldehyde

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate
72509-76-3,86189-69-7

ethyl methyl 1,4-dihydro-2,6-dimethyl-4(2,3-dichlorophenyl)-3,5-pyridinedicarboxylate

4-(-2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid methyl ester
91189-59-2

4-(-2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid methyl ester

4-(2,3-dichloro-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester
79925-38-5

4-(2,3-dichloro-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester

Conditions
Conditions Yield
acetoacetic acid methyl ester; 2,3-dichlorobenzylaldehyde; piperidine; 2-Picolinic acid; In isopropyl alcohol; at 40 - 45 ℃; for 6h;
ethyl aminocrotonate; In isopropyl alcohol; for 4h; Heating / reflux;
66%

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    Dehydrofelodipine

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