71879-55-5

Basic information

• Product Name: ETHYL 3-PIPERIDIN-4-YLPROPANOATE
• Synonyms: 3-Piperidin-4-yl-propionic acid ethyl ester;3-(4-piperidinyl)propanoic acid ethyl ester;ethyl 3-(4-piperidyl)propanoate;ETHYL 3-PIPERIDIN-4-YLPROPANOATE;4-piperidinepropanoic acid, ethyl ester;4-(2-Ethoxycarbonylethyl)piperidine;Ethyl 4-piperidinepropanoate
• CAS NO: 71879-55-5
• Molecular Formula: C₁₀H₁₉NO₂
• Molecular Weight: 185
• Mol File: 71879-55-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 252℃
• Flash Point: 106℃
• Appearance: /
• Density: 0.959
• CAS DataBase Reference: ETHYL 3-PIPERIDIN-4-YLPROPANOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 3-PIPERIDIN-4-YLPROPANOATE(71879-55-5)
• EPA Substance Registry System: ETHYL 3-PIPERIDIN-4-YLPROPANOATE(71879-55-5)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 71879-55-5(Hazardous Substances Data)

Usage

General Description

ETHYL 3-PIPERIDIN-4-YLPROPANOATE is a chemical compound with the molecular formula C12H21NO2. It is a derivative of piperidine, a heterocyclic organic compound. This chemical is commonly used in the pharmaceutical industry as an intermediate for the synthesis of various drugs and active pharmaceutical ingredients. It is also used in the production of agrochemicals, fragrances, and flavors. ETHYL 3-PIPERIDIN-4-YLPROPANOATE has a role as a flavoring agent and a plant metabolite. It is known for its mild, fruity odor and is often used to add a pleasant smell to products such as perfumes, soaps, and lotions.

Upstream product

• 123293-78-7 ethyl 3-(4-pyridinyl)-(2E)-propenoate 
• 84228-93-3 3-(pyridin-4-yl)acrylic acid 
• 1822-32-8 3-(4-piperidyl)propionic acid 
• 137076-22-3 tert butyl 4-formylpiperidine-1-carboxylate 
• 301232-45-1 tert-butyl 4-(3-ethoxy-3-oxopropyl)-1-piperidinecarboxylate 
• 162504-86-1 t-butyl 4-(3-ethoxy-3-oxoprop-1-enyl)-tetrahydropyridine-1(2H)-carboxylate 
• 24489-96-1 ethyl 3-(pyridin-4-yl)prop-2-enoate 
• 123855-51-6 tert-butyl 4-(hydroxymethyl)piperidin-1-carboxylate 
• 664364-13-0 benzyl 4-((1E)-3-ethoxy-3-oxoprop-1-en-1-yl)piperidine-1-carboxylate 
• 872-85-5 pyridine-4-carbaldehyde 

Downstream Products

• 1305197-29-8 N-hydroxy-3-(1-phenylmethanesulfonyl-piperidin-4-yl)-propionamide 
• 1305197-30-1 3-(1-benzenesulfonyl-piperidin-4-yl)-N-hydroxy-propionamide 
• 1305197-32-3 N-hydroxy-3-(1-phenylacetyl-piperidin-4-yl)-propionamide 
• 374776-40-6 4-(5-(4-(2-ethoxycarbonylethyl)piperidinylsulfonyl)-2-n-propoxybenzamido)-1-methyl-3-n-propylpyrazole-5-carboxamide 
• 374776-39-3 4-(2-ethoxy-5-(4-(2-ethoxycarbonylethyl)piperidinylsulfonyl)benzamido)-1-methyl-3-n-propylpyrazole-5-carboxamide 
• 301232-45-1 tert-butyl 4-(3-ethoxy-3-oxopropyl)-1-piperidinecarboxylate 
• 99197-86-1 ethyl 1-[(phenylmethoxy)carbonyl]-4-piperidinepropanoate 
• 51144-70-8 ethyl 3-(1-benzoylpiperidin-4-yl)propanoate 
• 124438-69-3 3-(1-Benzyl-piperidin-4-yl)-propionic acid,ethyl ester 
• 1454273-55-2 1'-benzyl-6,7-dihydrospiro[cyclopenta[d]pyrimidine-5.4'-piperidine]-2,4-(1H,3H)-dione 
• 1454273-54-1 ethyl 8-benzyl-2-ureido-8-azaspiro[4.5]dec-1-ene-1-carboxylate 
• 1454273-53-0 ethyl 8-benzyl-2-oxo-8-azaspiro[4.5]decane-1-carboxylate 
• 1454273-52-9 ethyl 5-(1-benzylpiperidin-4-yl)-2-diazo-3-oxopentanoate 
• 1454273-51-8 ethyl 5-(1-benzylpiperidin-4-yl)-3-oxopentanoate 

Relevant articles and documents

PRODUCTION METHOD OF CYCLIC COMPOUND

PROBLEM TO BE SOLVED: To provide an industrially simple production method of a cyclic compound. SOLUTION: A production method of a cyclic compound includes a step to obtain a reduced form (B) by reducing an unsaturated bond in a ring structure of an aromatic compound (A) by means of catalytic hydrogenation of the aromatic compound (A) or its salt using palladium carbon as a catalyst under a normal pressure, in which the aromatic compound (A) has one or more ring structures selected from a group consisting of a five membered-ring, a six membered-ring, and a condensed ring of the five membered-ring or the six membered-ring with another six membered-ring, a hetero atom can be included in the ring structure, and the aromatic compound (A) can have one or two side chains bonded to the ring structure and does not have any carbon-carbon triple bond in the side chain. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

SPIRO AZETIDINE ISOXAZOLE DERIVATIVES AND THEIR USE AS SSTR5 ANTAGONISTS

Provided is a compound represented by the following formula (1) or a salt thereof, which has an SSTR5 antagonistic action: wherein each symbol has the same definition as in the specification.

FUSED BENZENE DERIVATIVE AND USE

The present invention provides a compound represented by the general formula: [wherein Ring A represents an optionally substituted 5- to 8-membered ring, Ring B represents a further optionally substituted 4- to 10-membered ring, Ring C represents a further optionally substituted benzene ring, X1 represents carbon atom, X2 represents a carbon atom, an oxygen atom, etc., W represents a nitrogen atom, etc., Y11 represents a group represented by the formula CR2R3' (wherein R2 represents a hydrogen atom, a cyano group, a nitro group, etc., and R3' represents a hydrogen atom, a cyano group, a nitro group, etc., respectively), Y21 represents a group represented by the formula CR4R5' (wherein R4 represents a hydrogen atom, a cyano group, a nitro group, etc., and R5' represents a hydrogen atom, a cyano group, a nitro group, etc., respectively), etc., and R1 represents an electron-withdrawing group, respectively. The formula represents a single bond or a double bond] or a salt thereof, which is useful as an androgen receptor modulator.