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2-Pheny

CijHgNj. Made by heating o-pheny-lenediamine with glycerol, nitrobenzene and cone, sulphuric acid. It exists as a monohydrate, m.p. 94" C, or anhydrous, m.p. 117°C. It is used as a complexing reagent in the estimation of Fe and in the preparation of numer-... [Pg.303]

Diamino-4-phenylthiazole condenses with benzaldehyde, yielding 2-amino-4-pheny]-5-benzalaminothiazole (241). [Pg.47]

Phenyliinino-3-benzoylamino-4-thiazoline (412) rearranges in basic medium to 2-anilino-5-pheny -l,3,4-oxadiazole (413) (Scheme 236) 730). [Pg.132]

An example of the electrophilic reactivity of the C-4 atom is the easy formation of oxime and phenylhydrazone derivatives (422). It has been reported, however, that 2 pheny -A-2-thiazoline-4-one does not react with phenylhydrazine (397). [Pg.425]

For example, N-propynylbenzamides lead to 2-pheny]-5-methyl-thiazole (10), Rj = phenyl, R2 = H. Rj = methyl (562). [Pg.282]

Asinger and Thiel (473) use an aldehyde and ammonia instead of nitrile. Thus the reaction of mercaptoacetone. with benzaldehyde and ammonia gives 4 methyl-2-phenylthiazole in 80% yield and 4-methyl-2-pheny]-A-4-thiazoline as the main by-product. [Pg.293]

Pyrimidine-5-carboxamide, 4-amino-purine synthesis from, 5, 582 Pyrimidine-5-carboxamide, 4-amino- N- pheny synthesis, 3, 122 Pyrimidinecarboxamides Curtius degradation, 3, 82 dehydration, 3, 82 Hofmann degradation, 3, 82 hydrolysis, 3, 81 reactions, 3, 81 synthesis, 3, 127 Pyrimidinecarboxamides, thio-synthesis, 3, 128... [Pg.806]

Thiadiazole, 2-methyl-5-pheny 1-reactions with butyllithium, 6, 563... [Pg.862]

Cls-l,2,3,3a,4,8b-Hexahydro-4-forinyl-8b-ethylcyclopent(b)lndole. (2). Pheny iydra2one 1 (850 tng, 4.2 mmol) was trealed w ith98% HCOOH (902 mg, 19.6 mmol), 8era short exothermic reaction the mixture was heated at 130-135°C for 35 min. Evaporation HCOOH, extraction with EtOAc arxt chromatography on alumina (PhH) aflorded 246 mg i (25.6%). [Pg.123]

Carcinogens Cancer-producing agents Skin Respiratory Bladder/urinary tract Liver Nasal Bone marrow Coal tar pitch dust crude anthracene dust mineral oil mist arsenic. Asbestos polycyclic aromatic hydrocarbons nickel ore arsenic bis-(chloromethyl) ether mustard gas. p-naphthylamine benzidine 4-am i nodi pheny lam ine. Vinyl chloride monomer. Mustard gas nickel ore. Benzene. [Pg.69]

Thus the unsaturated ketones carvone, eucarvone and 1-acetyl-cyclohexane formed the cyclopropyl ketones (6), (7) and (8) while benzalaceto-phenone (9) affords l-benzyl-2-pheny 1-cyclopropane as a mixture of as and irons isomers (10) and (H) 233,234... [Pg.114]


See other pages where 2-Pheny is mentioned: [Pg.366]    [Pg.141]    [Pg.142]    [Pg.410]    [Pg.537]    [Pg.439]    [Pg.802]    [Pg.991]    [Pg.229]    [Pg.262]    [Pg.87]    [Pg.385]    [Pg.399]    [Pg.412]    [Pg.412]    [Pg.412]    [Pg.432]    [Pg.481]    [Pg.484]    [Pg.484]    [Pg.484]    [Pg.572]    [Pg.686]    [Pg.686]    [Pg.686]    [Pg.891]    [Pg.50]    [Pg.17]    [Pg.839]    [Pg.147]    [Pg.323]    [Pg.482]    [Pg.94]    [Pg.264]   


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1 -Pheny 1-2-buten

1 -Pheny 1-4- naphthalene

1 -Pheny lethylamine

1- Pheny 1-1,3-butadiene

1- ethyl pheny

1-Methyl-4-pheny tetrahydropyridine

2- pheny] methyl

3- - 3-pheny 11-propanone

4- cyano-2-pheny

5- pheny,amino

Lithium, [2- pheny

Methyl pheny, ketone

O-Pheny lenediamine

P-Pheny lenediamine

Pheny (acetate

Pheny lamine

Pheny lethy lamines

Pheny lseleno etherification

Pheny lseleno etherification intramolecular

Pheny lseleno etherification lactones

Pheny lurea herbicide

Pheny polymerization

Pheny(phosphate

Pheny] azide

Pheny] propyl

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