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  1. pubchem.ncbi.nlm.nih.gov › substance › 162228975SID 162228975 - PubChem

    Substance record SID 162228975 for 1-Bromobutane submitted by Chembase.cn.

  2. 1-Bromobutane, also known as n-butyl bromide is a primary alkyl halide, with the formula CH 3 CH 2 CH 2 CH 2 Br . It is colorless liquid, insoluble in water, but soluble in ethanol and ether; melting point -112 C; boiling point 101 - 102 C. It is used as an alkylating agent to introduce the butyl groups to form carbon-carbon bonds in organic ...

  3. Tuning the porosity of triangular supramolecular adsorbents for superior haloalkane isomer separations. PMID 34603658; DOI 10.1039/d1sc03509f; Chemical science 2021 Sep; 12 (37):12286-12291. Name matches: 1-chlorobutane 1-bromobutane. Negative-mode ion mobility spectrometry-comparison of ion-molecule reactions and electron capture processes.

  4. 1-Bromobutane is used as an intermediate in organic synthesis and as a solvent for cleaning and degreasing. It acts as an alkylating agent as well as to prepare organometallic compounds such as n-butyllithium. It is also involved in the synthesis of procaine and tetracaine. It reacts with magnesium metal to prepare the Grignard reagent, which ...

  5. Jun 01, 1995 · The rotational spectrum of 1-bromobutane has been measured in the range of 8-18 GHz using a 480 MHz bandwidth chirped-pulse Fourier transform microwave (CP-FTMW) spectrometer. 1-bromobutane has ...

  6. Gas-phase electron diffraction (ED), together with ab initio molecular orbital calculations, have been used to determine the structure and conformational composition of 1-chlorobutane, 1-bromobutane, and 1-iodobutane. These molecules may in principle exist as mixtures of five different conformers, but only three or four of these were observed in gas phase at temperatures of the ED experiments ...

  7. Draw the structure of following compounds, determine which one has an chirality center and label it with a star. a) 1-bromobutane, b) 1-pentanol, c) 2-pentanol, d) 3-pentanol, e) 2-bromopropanoic acid. f) 2-methyl cyclohexanone 2. Label all the chirality centers in the following molecules.

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