23692-08-2

Basic information

• Product Name: 2-Piperidineacetic acid, methyl ester
• CAS NO: 23692-08-2
• Molecular Formula: C8H15NO2
• Molecular Weight: 157.213
• Mol File: 23692-08-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-Piperidineacetic acid, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Piperidineacetic acid, methyl ester(23692-08-2)
• EPA Substance Registry System: 2-Piperidineacetic acid, methyl ester(23692-08-2)

Safety Data

• Hazardous Substances Data: 23692-08-2(Hazardous Substances Data)

Upstream product

• 2739-98-2 ethyl 2-(pyridinyl-2)acetate 
• 67-56-1 methanol 
• 19615-30-6 piperidin-2-yl-acetic acid hydrochloride 
• 85274-59-5 N-phenyl-2-(pyridin-2-yl)acetamide 
• 1620-53-7 1-phenyl-2-pyridin-2-ylethanone 
• 61890-12-8 1-phenyl-2-[2]pyridyl-ethanone-(E)-oxime 
• 34418-91-2 2,3,4,5-tetrahydropyridine N-oxide 
• 1484-84-0 2(RS)-(2-hydroxyethyl)piperidine 
• 19832-04-3 2-(piperidin-2-yl)acetic acid 
• 150931-54-7 methyl (1-benzoyloxypiperidin-2-yl)acetate 
• 13115-43-0 2-pyridineacetic acid 
• 1658-42-0 methyl 2-pyridylacetate 

Downstream Products

• 847030-13-1 (+/-)-4-methyl-3-(p-toluenesulfonyl)-3,4-dehydroquinolizidin-2-one 
• 1163790-27-9 pTosGlp-OH methyl 2-(piperidyl)-acetate salt 
• 1190971-02-8 [1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-2-yl]-acetic acid methyl ester 
• 171730-95-3 methyl (R)-(2-piperidino)acetate 
• 171866-64-1 (2S)-methoxycarbonylmethylpiperidin 
• 174822-16-3 2-chloro-5-methoxy-4-<5-(2-piperidylmethyl)-1,2,4-oxadiazol-3-yl>aniline 

Relevant articles and documents

HEPATITIS B CORE PROTEIN MODULATORS

The present disclosure provides, in part, compounds having allosteric effector properties against Hepatitis B virus Cp. Also provided herein are methods of treating viral infections, such as hepatitis B, comprising administering to a patient in need thereof a disclosed compound of formula:

NEW ANTIBACTERIAL COMPOUNDS

The present invention is related to novel compounds of formula (I) that may inhibit the activity of the FabI enzyme, and which are useful in the treatment of bacterial infections. It further relates to pharmaceutical compositions comprising these compound

Synthesis of the quinolizidine alkaloids (-)-lasubine II and (±)-myrtine by conjugate addition and intramolecular acylation of amino esters with acetylenic sulfones

(Chemical Equation Presented) The conjugate additions of (2-piperidyl)acetate esters to acetylenic sulfones, followed by LDA-promoted intramolecular acylations, afforded cyclic enaminones that were readily converted into the corresponding 4-substituted 2-