1,4-二溴丁烷

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1,4-二溴丁烷
识别
CAS号 110-52-1  checkY
SMILES
 
  • BrCCCCBr
性质
化学式 C4H8Br2
摩尔质量 215.91 g·mol−1
密度 1.8269 g·cm−3(20 °C)[1]
熔点 −16.5 °C[2]
沸点 197 °C[2]
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

1,4-二溴丁烷是一种有机化合物,属卤代烃,化学式为C4H8Br2,可由1,4-丁二醇(或四氢呋喃[3])和HBr反应得到。[4]它和仲胺反应,得到叔胺,通过进一步反应来得到双子型季铵盐[5]

参考文献

  1. ^ E. V. Whitehead, R. A. Dean, F. A. Fidler. The Preparation and Physical Properties of Sulfur Compounds Related to Petroleum. II. Cyclic Sulfides 1. Journal of the American Chemical Society. 1951-08, 73 (8): 3632–3635 [2020-05-29]. ISSN 0002-7863. doi:10.1021/ja01152a022 (英语). 
  2. ^ 2.0 2.1 "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2020-05-14]
  3. ^ Christopher L. Wilson. 15. Reactions of furan compounds. Part II. Fission of the tetrahydrofuran and the tetrahydropyran ring. Journal of the Chemical Society (Resumed). 1945: 48 [2020-05-29]. ISSN 0368-1769. doi:10.1039/jr9450000048 (英语). 
  4. ^ Kurata, Takeo; Kurita, Nozomi. Synthesis of 17 membered-ring oxalactones and its odor characteristics. Fain Kemikaru, 2008. 37 (2): 43-49. ISSN: 0913-6150.
  5. ^ Jiaul Hoque, Pratik Kumar, Vinod K. Aswal, Jayanta Haldar. Aggregation Properties of Amide Bearing Cleavable Gemini Surfactants by Small Angle Neutron Scattering and Conductivity Studies. The Journal of Physical Chemistry B. 2012-08-16, 116 (32): 9718–9726 [2020-05-29]. ISSN 1520-6106. doi:10.1021/jp305590f. (原始内容存档于2020-11-28) (英语).