1,4-二溴丁烷

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1,4-二溴丁烷
識別
CAS號 110-52-1  checkY
SMILES
 
  • BrCCCCBr
性質
化學式 C4H8Br2
摩爾質量 215.91 g·mol−1
密度 1.8269 g·cm−3(20 °C)[1]
熔點 −16.5 °C[2]
沸點 197 °C[2]
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

1,4-二溴丁烷是一種有機化合物,屬鹵代烴,化學式為C4H8Br2,可由1,4-丁二醇(或四氫呋喃[3])和HBr反應得到。[4]它和仲胺反應,得到叔胺,通過進一步反應來得到雙子型季銨鹽[5]

參考文獻[編輯]

  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 (英語). 
  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 (英語). 
  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. (原始內容存檔於2020-11-28) (英語).