碘代正丁烷
一般危化品
碘代正丁烷结构式
|
常用名 | 碘代正丁烷 | 英文名 | Butyl iodide |
|---|---|---|---|---|
| CAS号 | 542-69-8 | 分子量 | 184.019 | |
| 密度 | 1.6±0.1 g/cm3 | 沸点 | 130.9±3.0 °C at 760 mmHg | |
| 分子式 | C4H9I | 熔点 | −103 °C(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 33.3±0.0 °C | |
| 符号 |
GHS02, GHS06 |
信号词 | Danger |
|
Replacement surgery with unnatural amino acids in the lock-and-key joint of glutathione transferase subunits.
Chem. Biol. 13(9) , 929-36, (2006) Proteins contain amino acid residues essential to structure and function. Ribosomal protein synthesis is typically limited to the 20 amino acids of the genetic code, but posttranslational chemical modifications can greatly expand the diversity of side chain f... |
|
|
Invoking pairwise interactions in water-promoted Diels-Alder reactions by using ionic liquids as cosolvents.
ChemPhysChem 15(14) , 3067-77, (2014) Rate constants and derived activation parameters of organic reactions in aqueous media, in particular Diels-Alder reactions, are sensitive to the presence of cosolvents in water. To enhance the solubility window of water, we introduced ionic liquids as cosolv... |
|
|
Determination of trace level genotoxic impurities in small molecule drug substances using conventional headspace gas chromatography with contemporary ionic liquid diluents and electron capture detection.
J. Chromatogr. A. 1361 , 217-28, (2014) Ionic liquids (ILs) were used as a new class of diluents for the analysis of two classes of genotoxic impurities (GTIs), namely, alkyl/aryl halides and nitro-aromatics, in small molecule drug substances by headspace gas chromatography (HS-GC) coupled with ele... |
|
|
Reaction of tributyl phosphite with oxidized iron: surface and tribological chemistry.
Langmuir 20(18) , 7557-68, (2004) The surface chemistry of a model lubricant additive, tributyl phosphite (TBPi), is investigated on Fe3O4 in ultrahigh vacuum. A portion of the TBPi desorbs molecularly following adsorption at approximately 200 K, the remainder decomposing either by C-O bond s... |
|
|
Synthesis of 5-(2-,3- and 4-methoxyphenyl)-4H-1,2,4-triazole-3-thiol derivatives exhibiting anti-inflammatory activity.
Il Farmaco 59(4) , 255-9, (2004) New S-alkylated 5-(2-,3- and 4-methoxyphenyl)-4H-1,2,4-triazole-3-thiols (5a-c, 6a-c) and 5-(2-,3- and 4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazole-3-thiols (7a-c, 8a-c, 9a-c) were synthesized by the alkylation of 3-(2-,3- and 4-methoxyphenyl)-4,5-dihydro-1H-1... |
|
|
Recent developments in the ENEA lithium metal battery project. Shin J-H, et al.
Electrochim. Acta 50(19) , 3859-65, (2005)
|
|
|
Thermal chemistry of C4 hydrocarbons on Pt(111): Mechanism for double-bond isomerization.
J. Phys. Chem. B 109(7) , 2745-53, (2005) The thermal chemistry of a number of C4 hydrocarbons (1,3-butadiene, 1-bromo-3-butene, 1-bromo-2-butene, trans-2-butene, cis-2-butene, 1-butene, 2-iodobutane, 1-iodobutane, and butane) was investigated on clean and hydrogen- and deuterium-predosed Pt(111) sin... |
|
|
Formation of 1-[123I]iodobutane in labeling [123I]iomazenil by iododestannylation: implications for the reaction mechanism.
Appl. Radiat. Isot. 45(1) , 63-8, (1994) The benzodiazepine receptor tracer [123I]iomazenil (Ro 16-0154, IMZ) can be prepared in close to theoretical specific activity by the reaction of its tributyltin precursor (IMZ-SnBu3) with [123I]NaI in the presence of Iodogen. However, the labeling reaction i... |