2-methylpiperidine

Carbamoyl chlorides are important intermediates both in the research laboratory and in industrial scale syntheses The most studied and used are the disubstituted derivatives incorporating either aryl or alkyl groups (Ar2NCOCl or R2NCOCl) Sometimes the groups are tied back to give a ring and piperidino- and morpholino-derivatives are commonly encountered The reaction of N-allenyl-N-allyl-p-toluenesulfonamide (1b 74 8 mg 0 30 mmol) with 2-methylpiperidine (42 3 μL 0 36 mmol 1 2 equiv) according to the general procedure (flash chromatography: EtOAc/petroleum ether 85:15) gave 2t (79 5 mg 76%) as a pale brown oil IR (ATR): 2928 2856 2791 1654 1598 1355 1306 1163 1090 664 cm –1

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2-methylpiperidine (English) retrieved 14 October 2016 SPLASH splash10-000j-9000000000-f6cd5eecf7ee9960906d 0 references Sitelinks Wikipedia (1 entry) edit eswiki 2-pipecolina Wikibooks (0 entries) edit Wikinews (0 entries) edit Wikiquote (0 entries) edit Wikisource (0 entries) edit Wikiversity (0 entries) edit Wikivoyage (0 entries)

Huamin Wang Changhai Liang and Roel Prins* Hydrodenitrogenation of 2-methylpyridine and its intermediates 2-methylpiperidine and tetrahydro-methylpyridine over sulfided NiMo/γ-Al2O3 J Catal 2007 251 295-306 Li Xing Jieshan Qiu* Changhai Liang Chuang Wang Li Mao A New Approach to High Performance Co/C Catalysts for selective Hydrogenation of Chloronitrobenzene J Catal

TECHNIC The same technic of administration was employed as originally described by Edwards and Hingson 1 with the precaution of waiting ten minutes after a test injection of 8 cc (90 mg ) of a 1 5 per cent solution of metycaine (γ-[2-methylpiperidine]-propanol hydrochloride) 2 This caution was exercised to make certain that the solution did not enter the subarachnoid space If signs of

Khaled and Amin studied the adsorption and corrosion inhibition behaviour of four selected piperidine derivatives namely piperidine (pip) 2-methylpiperidine (2mp) 3-methylpiperidine (3mp) and 4-methylpiperidine (4mp) at nickel in 1 0 M HNO 3 solution computationally by the molecular dynamics simulation and quantum chemical calculations and electrochemically by Tafel and impedance methods

(S)-2-methylpiperidine(7 3ml 62 0mmol)andpyri-dine(5 3ml 62 0mmol)indichloromethane(25ml) was added The resulting mixture was stirred over-nightatroomtemperature Afteradditionofwater(15 ml) the organic layer was separated washed with saturatedaqueousNaHCO 3(20ml) brine(20ml) 2% HCl (20 ml) again with brine (20 ml) and dried (MgSO

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2-methylpiperidine: Instrument: Not specified most likely a prism grating or hybrid spectrometer Path length: SMEAR: Resolution: 4: Sampling procedure: TRANSMISSION: Data processing: DIGITIZED BY NIST FROM HARD COPY: This IR spectrum is from the Coblentz Society's evaluated infrared reference spectra collection References Go To: Top Infrared Spectrum Notes Data compilation copyright

In 3 series of field tests 6 repellent compounds were evaluated against the black flies Simulium venustum and Prosimutium mixtum at Baxter State Park Maine All chemicals tested equalled the deet [diethyltoluamide] (N N-diethyl-m-toluamide) (A13-22542) standard in effectiveness One compound [1-(3-cyclohexen-1-ylcarbonyl)piperidine] (A1335765) provided over 8 h average protection while the

Reprotection and hydrogenation effected reduction of the endocyclic alkene bond without affecting the sterically encumbered exocyclic alkene bond Acidic deprotection yielded himbeline (166a) and reductive methylation himbacine (166b) in 11 steps and a remarkable overall yield of 9 7% from (S)-2- methylpiperidine L-tartrate

A 13 C dynamic NMR of meso-1 1′-bi (2-methylpiperidine) s revealed that the barrier to the single-passing rotation about the N–N bond was at least 74 1 kJ mol −1 which was considerably higher than the barrier to the passing inversion of the nitrogen atom View full abstract View on the journal site STEREOSELECTIVE FORMATION OF α α-DIAMINO ACID RESIDUE BY THE ADDITION OF L-α

2-methylpiperidine C6H13N x͈́51 48 ` 157 53 cyclohexylamine C6H13N x͈́60 72 ` 128 37 hexane C6H14 x͈́27 11 ` 48 11 n-hexane C6H14 x͈́27 11 ` 48 11 hexane C6H14 x͈́-95 44 ` -8 21 n-hexane C6H14 x͈́-95 44 ` -8 21 hexane C6H14 x͈́25 08 ` 69 67 n-hexane C6H14 x͈́25 08 ` 69 67 2_2-dimethylbutane C6H14 x͈́-62 16 ` 16 23 hexane C6H14

C 8 H 15 NO est la formule brute de plusieurs isomres Alcool tropanol tropine numro CAS pseudotropine numro CAS exo-8-mthyl-8-azabicyclo[3 2 1]octane-3-ol numro CAS 2-mthylquinuclidine-3-ol numro CAS Ctone hygrine numro CAS pelletirine ou 1-pipridin-2-ylpropan-2-one numro CAS 1-(2-pipridyl)propan-2-one numro CAS mlange racmique des

[0006] The histamine-3 (H 3) receptor was first characterized pharmacologically on histaminergic nerve terminals (Nature 302:832-837 (1983)) where it regulates the release of neurotransmitters in both the central nervous system and peripheral organs particularly the lungs cardiovascular system and gastrointestinal tract H 3 receptors are thought to be disposed presynaptically on

Tables of 1H and 13C NMR chemical shifts have been compiled for common organic compounds often used as reagents or found as products or contaminants in deuterated organic solvents Building upon the work of Gottlieb Kotlyar and Nudelman in the Journal of Organic Chemistry signals for common impurities are now reported in additional NMR solvents (tetrahydrofuran-d8 toluene-d8

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Visit ChemicalBook To find more 2-Methylpiperidine(109-05-7) information like chemical properties Structure melting point boiling point density molecular formula molecular weight physical properties toxicity information customs codes You can also browse global suppliers vendor prices Price manufacturers of 2-Methylpiperidine(109-05-7) At last 2-Methylpiperidine

1 In cats anaesthetized with I P pentobarbitone sodium and atropinized with intravenous atropine methyl nitrate the effects on arterial blood pressure were examined of nicotine physostigmine carbachol glycine and pentobarbitone sodium applied to the exposed ventral surface of the brain stem by means of paired Perspex rings placed across the medulla

Out of the biotransformations that worked well at 100 mM substrate concentration two were chosen for reactions at preparative scale (5 mmol): Imine 1 b was reduced by IRED‐J to (S )‐2‐methylpiperidine (2 b ) which was isolated as the corresponding acetamide derivative in 74 % yield and 99 % ee

Temperature perception has long been classified as a somesthetic function solely However in recent years several studies brought evidence that temperature perception also takes place in the olfactory system of rodents Temperature has been described as an effective stimulus for sensory neurons of the Grueneberg ganglion located at the entrance of the nose

2-methylpiperidine Regulatory process names 1 IUPAC names 1 Other identifiers 1 Print infocard Substance identity Substance identity The 'Substance identity' section is calculated from substance identification information from all ECHA databases The substance identifiers displayed in the InfoCard are the best available substance name EC number CAS number and/or the molecular and

AChemBlock offers K10845 (2S 4S)-2-methyl-4-methoxylpiperidine hydrochloride for your research Find product's price/availability shipping time in our secure Ecommerce website Try our new powerful structure search function Category: piperidine IUPAC Name: (2S 4S)-4-methoxy-2-methylpiperidine hydrochloride CAS No : 1421253-05-5 MDL: MFCD28401055

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