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Methyl iodine

Imidazole, 4,5-dibromo-l-methyl-synthesis, S, 399 Imidazole, 4,5-di-t-butyl-synthesis, S, 483 X-ray diffraction, S, 350 Imidazole, 4,5-dichloro-chlorination, S, 398 synthesis, S, 398, 473 Imidazole, 4-(3,4-dichlorophenyl)-nitration, 5, 433 Imidazole, 4,5-dicyano-hydrolysis, S, 435-436 synthesis, S, 461, 472, 487 Imidazole, 4,5-dicyano-1-vinyl-synthesis, S, 387 Imidazole, 4,5-dihydro-mass spectra, 5, 360 Imidazole, 4-(dihydroxybutyl)-synthesis, S, 484 Imidazole, 4,5-diiodo-nitration, S, 396 synthesis, S, 400 Imidazole, 2,4-diiodo-5-methyl-iodination, S, 400 Imidazole, 1,2-dimethyl-anions... [Pg.651]

Imidazole, 1 -hydroxy-2,4,5-triphenyl-3-oxides reactions, S, 455 Imidazole, iodo-nitrodehalogenation, 5, 396-397 Imidazole, 1-iodo-reactions, S, 454 stability, S, 110 Imidazole, 2-iodo-synthesis, S, 401 Imidazole, N-iodo-, S, 393 reactions, 5, 454 Imidazole, 4-iodo-5-methyl-iodination, 5, 400 Imidazole, 2-isopropyl-4-nitro-N-nitration, 5, 351 Imidazole, 2-lithio-reactions, S, 106, 448 Imidazole, 2-mercapto-l-methyl-as antithyroid drug, 1, 171 mass spectra, 5, 358 Imidazole, 1-methoxymethyl-acylation, S, 402 Imidazole, 5-methoxy-l-methyl-reactions... [Pg.652]

Aluminum methyl Iodine azide Radio isotopes, gamma emitters... [Pg.1026]

Alkylating reagents such as boron trifluoride-methanol, sulfuric acid-methanol, methanol-hydrochloric acid and methyl iodine-sodium hydride do not react efficiently with pyrithiobac. Trimethylsilyldiazomethane may be used for the methyl-ation of pyrithiobac. [Pg.563]

The Liotta procedure involved slurrying coal in an aqueous solution of tetrabutylammonium hydroxide to remove acidic protons, followed by addition of methyl iodide as alkylating agent. This mixture was then stirred vigorously for 12-72 hrs. depending upon the extent of alkylation desired. After all lation, the moist coal sample was roto-evaporated to remove excess THF and methyl iodine, followed by exdiaustive extraction with water to remove tetrabutylammonium iodide produced during all lation. Finally, the treated coal was vacuum dried (50 C, 0.1 torr, 24 hours) before use. [Pg.262]

Eight benzimidazoles Animal tissues ACN extn, liq-liq partns, two SPE cleanups 24 Hewlett-Packard RP-18,5 m, with Kontron RP-18 Presat, 25-40 m, guard column O.OIM pentane-sulfonate contg 0.5% TEA, pH 3.5/ACN (50 50) UV 298 nm/ 20-50 ppb/ GC-NPD 39-87% or GC-EI-MS or GC-Pulsed PICI-NICI-MS after derivatization with methyl iodine or pentafluoro- benzyl bromide 358... [Pg.1024]

Dieckmann reaction, 4, 471 Indolizidine alkaloids mass spectra, 4, 444 Indolizidine immonium salts reactions, 4, 462 Indolizi dines basicity, 4, 461 circular dichroism, 4, 450 dipole moments, 4, 450 IR spectra, 4, 449 reactivity, 4, 461 reviews, 4, 444 stereochemistry, 4, 444 synthesis, 4, 471-476 Indolizine, 1-acetoxy-synthesis, 4, 466 Indolizine, 8-acetoxy-hydrolysis, 4, 452 synthesis, 4, 466 Indolizine, l-acetyl-2-methyl-iodination, 4, 457 Indolizine, 3-acyloxy-cyclazine synthesis from, 4, 460 Indolizine, alkyl-UV spectra, 4, 449 Indolizine, amino-instability, 4, 455 synthesis, 4, 121 tautomerism, 4, 200, 452 Indolizine, 1-amino-tautomerism, 4, 38 Indolizine, 3-amino-synthesis, 4, 461, 470... [Pg.672]

The process of methylation with C-11 methyl iodine eventually became widely used for labeling many drugs. To produce C-11, because of its 20-minute half-life, it is necessary to have a cyclotron close to where the chemical syntheses and imaging procedures are carried out. [Pg.39]

Arylsulfonyl)methyl]iodine(III) bis(trifluoroacetates) 41 can be prepared from the respective iodomethyl sulfones 40 using a similar oxidation procedure (Scheme 2.20) [138]. Bis(trifluoroacetates) 41 can be isolated at 0 °C, but are unstable at room temperature and can spontaneously decompose with explosion. [Pg.38]

Photodissociation dynamics of methyl iodine starting from the A(n-c ) band excitation has been subject to extensive experimental and theoretical studies. Recent experimental... [Pg.47]

III-23. The usual, conservative, approach is to neglect the solubility of noble gases in the pool water. However, a significant fraction of the iodine and caesium will be retained in the pool water. The release of iodine into the atmosphere above the pool may best be described in terms of a partition coefficient (the ratio of the volumetric activity concentrations (Bq/m ) in air and in water). For that part of the iodine present in organic compounds such as methyl iodine no solubility in water is conservatively assumed in many States. [Pg.88]

Vinyl esters n-Vinyl 5-methyl- Iodine number of... [Pg.26]


See other pages where Methyl iodine is mentioned: [Pg.38]    [Pg.182]    [Pg.251]    [Pg.29]    [Pg.140]    [Pg.29]    [Pg.1386]    [Pg.22]    [Pg.115]    [Pg.251]    [Pg.45]    [Pg.279]    [Pg.36]    [Pg.894]    [Pg.13]    [Pg.344]    [Pg.220]    [Pg.169]    [Pg.14]   
See also in sourсe #XX -- [ Pg.455 ]




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Imidazole, 4-methyl-, iodination

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