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Piperazin

The hexahydrate fonns colourless crystals, m.p. 44 C (104 C when anhydrous), b.p. 126 C. Made by the action of alcoholic ammonia on 1,2-dichloroethane, piperazine is used in human and veterinary medicine in the treatment of threadworm and roundworm infestations. [Pg.315]

B) Secondary amines, (i) Aromatic amines. Monomethyl and monoethylaniline, diphenylamine. (ii) Aliphatic and other amines. Diethyhmine, di-n-propylamine, di-isopropylamine. Also piperidine piperazine diethylene-diamine). [Pg.317]

Tetrahydroquinoline Tetrahydro-iso-quinoline Indole Carbazole Piperazine... [Pg.659]

XXIII xxin, 1st 1936 3458-3554 Two Cyclic Nitrogens. Stem nuclei Piperazine, 4. Diazo-... [Pg.1124]

A series of compounded flame retardants, based on finely divided insoluble ammonium polyphosphate together with char-forming nitrogenous resins, has been developed for thermoplastics (52—58). These compounds are particularly useful as iatumescent flame-retardant additives for polyolefins, ethylene—vinyl acetate, and urethane elastomers (qv). The char-forming resin can be, for example, an ethyleneurea—formaldehyde condensation polymer, a hydroxyethylisocyanurate, or a piperazine—triazine resin. [Pg.476]

Many patents have been issued on the use of pyrogaUol derivatives as pharmaceuticals. PyrogaUol has been used extemaUy in the form of an ointment or a solution in the treatment of skin diseases, eg, psoriasis, ringworm, and lupus erythematosus. GaUamine triethiodide (16) is an important muscle relaxant in surgery it also is used in convulsive-shock therapy. Trimethoprim (2,4-diamino-5-(3,4,5-trimethoxybenzyl)pyrimidine) is an antimicrobial and is a component of Bactrin and Septra. Trimetazidine (l(2,3,4-trimethoxybenzyl)piperazine (Vastarel, Yosimilon) is used as a coronary vasodilator. l,2,3,4-Tetrahydro-6-methoxy-l-(3,4,5-trimethoxyphenyl)-9JT-pyrido[3,4- ]indole hydrochloride is useful as a tranquilizer (52) (see Hypnotics, sedatives, ANTICONVULSANTS, AND ANXIOLYTICS). Substituted indanones made from pyrogaUol trimethyl ether depress the central nervous system (CNS) (53). Tyrosine-and glycine(2,3,4-trihydroxybenzyl)hydrazides are characterized by antidepressant and anti-Parkinson activity (54). [Pg.378]

Significant quantities of amine and amide esters are formed by side reactions (9). In addition, with dialkanolamines, amide diesters, morpholines, and piperazines can be obtained, depending on the starting material. Reaction of dialkanolamines with fatty acids in a 2 1 ratio, at 140—160°C, produces a second major type of alkanolamide. These products, in contrast to the 1 1 alkanolamides, are water soluble they are complex mixtures of AJ-alkanolamides, amine esters, and diesters, and still contain a considerable amount of unreacted dialkanolamine, accounting for the water solubiUty of the product. Both the 1 1 and the 2 1 alkanolamides are of commercial importance in detergents. [Pg.5]

Classic A/-heterocychc ligands, eg, bipyridyl (bipy), terpyridyl, imidazole, pyrazine, phenanthroline, piperazine (including alkyl- and aryl-substituted derivatives), and polypyrazol-l-yl-borates (bis, tris, and tetra), have all been found to coordinate Th(IV) chlorides, perchlorates, and nitrates. The tripodal hydrotris(pyrazolyl)borates, HBPz, have been used to stabilize organometaHic complexes (31). Bis-porphyrin Th(IV) "sandwich" complexes have been... [Pg.37]


See other pages where Piperazin is mentioned: [Pg.315]    [Pg.375]    [Pg.550]    [Pg.425]    [Pg.533]    [Pg.16]    [Pg.572]    [Pg.776]    [Pg.878]    [Pg.878]    [Pg.892]    [Pg.892]    [Pg.937]    [Pg.937]    [Pg.937]    [Pg.937]    [Pg.1211]    [Pg.586]    [Pg.307]    [Pg.613]    [Pg.615]    [Pg.766]    [Pg.766]    [Pg.766]    [Pg.766]    [Pg.766]    [Pg.766]    [Pg.108]    [Pg.108]    [Pg.136]    [Pg.137]    [Pg.244]    [Pg.10]    [Pg.54]    [Pg.215]    [Pg.257]    [Pg.456]    [Pg.21]    [Pg.242]   
See also in sourсe #XX -- [ Pg.721 , Pg.787 , Pg.981 , Pg.1028 , Pg.1218 ]




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1 - piperazine reduction

1 - piperazine,4-alkylation

1 -Methyl-4- piperazine reduction

1- Ethoxycarbonyl-4- piperazine

1- Ethyl-4- piperazine

1- Methyl-4- piperazine acylation

1- nitrophenyl piperazines

1- piperazine, conformation

1- piperazine,hydrolysis

1- piperazines, oxidation

1-Piperazine ethyl acetate

1-pyrimidinyl piperazine

1.4- Disubstituted piperazines

2- piperazine chlorination

2-Trifluoromethyl-3- piperazine

2-[2- piperazine-2,5-dione

Amino Acids through Piperazine-2,5-diones

Aminoethyl piperazine

Applications of Piperazine-2,5-diones

Aryl piperazine

Benzhydryl piperazine

Benzhydryl piperazine Cinnarizine

Bis piperazine

Boc-piperazines

Butyl piperazine

Chlorpromazine piperazine

Dehydrogenation of piperazines to pyrazines

Hepatitis piperazine

Heterocyclic compounds piperazine

Imidazo piperazines

Isocyanate piperazine

Keto piperazine

L- piperazine

L- piperazine dihydrochloride

L- piperazines, oxidation

Mimedran - Sultosilic acid piperazine salt

N- piperazine

N-AMINOETHYL PIPERAZINE.252(Vol

N-Methyl piperazine

Naproxen piperazine

Neurotoxicity piperazine

Nitrogen, heterocyclic compounds piperazine

Oligomers piperazine-terminated

PIPERAZINE POLYMER

PIPERAZINE.292(Vol

Piperazin-2-one

Piperazin-2-ones 1,4-disubstituted

Piperazin-2-ones preparation

Piperazin-2-ones reactions

Piperazin-2-ones reviews

Piperazine 1-carboxylic acid ethyl ester

Piperazine 2.5- dioxo

Piperazine Ciprofloxacin

Piperazine N-alkylation

Piperazine Norfloxacin

Piperazine Perphenazine

Piperazine Prazosin

Piperazine Pyrantel

Piperazine adduct

Piperazine adipate

Piperazine amides

Piperazine analogs

Piperazine and derivs

Piperazine antihistamines

Piperazine antihistaminics

Piperazine carboxylation

Piperazine catalysis

Piperazine chemical solvent

Piperazine chemical structure

Piperazine citrate

Piperazine derivatives, cyclization with

Piperazine derivative—hydroxyzine

Piperazine diacetate

Piperazine dialkyl

Piperazine dihydrochloride

Piperazine estrone sulfate

Piperazine formation

Piperazine halogenation

Piperazine hexahydrate

Piperazine hydrate

Piperazine hydrochloride

Piperazine neuroleptic drugs

Piperazine nitrosation

Piperazine pharmacokinetics

Piperazine phenothiazines

Piperazine phosphate

Piperazine polyurethane

Piperazine reaction with, phosgene

Piperazine reactions

Piperazine reactivity

Piperazine reagent

Piperazine relative nucleophilicity

Piperazine resin

Piperazine ring

Piperazine salt

Piperazine synthesis

Piperazine, 1-benzyl

Piperazine, 2,5-diketobislactam ethers

Piperazine, 2,5-diketobislactam ethers metallated, reactions

Piperazine, 2,5-diketobislactam ethers regiochemistry of deprotonation

Piperazine, 2-methyl

Piperazine, Michael addition

Piperazine, N-alkylation with benzyl

Piperazine, N-alkylation with benzyl chloride

Piperazine, Phenazine, 1,3-Diazine

Piperazine, catalytic reaction

Piperazine, chiral

Piperazine, derivatives

Piperazine, derivatives reactions

Piperazine, diketo

Piperazine, ligand

Piperazine, physical properties

Piperazine, proton transfer

Piperazine, reaction + chloroformates

Piperazine, resin-bound

Piperazine, structure

Piperazine-1,4-bis(2-ethanesulfonic

Piperazine-1,4-diacetic acid

Piperazine-2, 5-diones, synthesis

Piperazine-2,3,5-trione

Piperazine-2,3-diones reviews

Piperazine-2,5-Dione Formation from Esters of Dipeptides

Piperazine-2,5-dione chlorination

Piperazine-2,5-dione derivatives

Piperazine-2,5-dione with triethyloxonium fluoroborate

Piperazine-2,5-diones

Piperazine-2,5-diones alkylation

Piperazine-2,5-diones and related lactim

Piperazine-2,5-diones and related lactim ethers

Piperazine-2,5-diones chlorination

Piperazine-2,5-diones conformation

Piperazine-2,5-diones preparations

Piperazine-2,5-diones reactions

Piperazine-2,5-diones, 3,6-disubstituted

Piperazine-2,5-dithione

Piperazine-2,5-dithiones

Piperazine-2,6-diones 4-unsubstituted

Piperazine-2-carboxamide

Piperazine-2-carboxylic acid

Piperazine-2-carboxylic acid peptides

Piperazine-2-thione

Piperazine-capped siloxane

Piperazine-terminated siloxane

Piperazines

Piperazines

Piperazines 2 molecules)

Piperazines 2-aminoalcohols

Piperazines Dinitrosopiperazines

Piperazines Subject

Piperazines bicyclic, condensed

Piperazines biological activity

Piperazines combinatorial library

Piperazines conformers

Piperazines dehydrogenation

Piperazines diastereoselective reactions

Piperazines dipole moments

Piperazines from diketopiperazines

Piperazines introduction

Piperazines metallated

Piperazines monoalkyl

Piperazines monocyclic

Piperazines piperazine-2-carboxamides

Piperazines polymer bound

Piperazines preparations

Piperazines properties

Piperazines reviews

Piperazines special

Piperazines toxicity

Piperazines, immobilized

Piperazino piperazines

Polar piperazines

Poly ]piperazine

Poly piperazine containing

Pyrazines and Piperazines

Pyrazines piperazines

Reactivity of Piperazine-2,5-diones

Sultosilic Acid Piperazine Salt

Synthesis of Piperazine-2,5-diones

Tetrazolo piperazines

Trans-2,5-Dimethyl piperazine

Triazolo piperazines

Tricyclic piperazines

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