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2-Bromobutane | CAS:78-76-2
2-Bromobutane
  • Name:2-Bromobutane
  • CAS:78-76-2
  • Synonyms:Methylethylbromoomethane; sec-Butyl bromide
  • Molecular Formula:C4H9Br
  • Molecular Weight:137.02
  • EINESC:201-140-7

Description

Properties

Melting point -112 ºC
Water Solubility Insoluble
Boiling point 91 ºC
Flash point 21 ºC
Density 1.255
Refractive index 1.4359-1.4379

Safety

Symbol(GHS) F;Xi
Hazard Codes R10;R11;R36/37/38
SDS/MSDS S16;S23;S24/25;S26;S37/39

SDS

Source SDS/MSDS Samples
没有数据没有数据
Synthetic Route
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Articles
Peer-Reviewed Papers
An extremely efficient three-component reaction of aldehydes/ketones, amines, and phosphites (Kabachnik-Fields reaction) for the synthesis of alpha-aminophosphonates catalyzed by magnesium perchlorate.Srikant Bhagat et al.The Journal of organic chemistry, 72(4), 1263-1270 (2007-01-27) Synthesis of a chitosan-dendrimer hybrid and its biodegradation.Hitoshi Sashiwa et al.Biomacromolecules, 4(5), 1244-1249 (2003-09-10) Synthesis, 3122-3122 (2006) Effect of surface modification and macrophage phenotype on particle internalization.Daniel Wang et al.Biomacromolecules, 15(11), 4102-4110 (2014-10-01) Altering in vivo macrophage responses with modified polymer properties.Hannah C Bygd et al.Biomaterials, 56, 187-197 (2015-05-03) Preparation of a mesoporous silica-based nano-vehicle for dual DOX/CPT pH-triggered delivery.Maria C Llinàs et al.Drug delivery, 25(1), 1137-1146 (2018-05-22) Triamino derivatives of triazolotriazine and triazolopyrimidine as adenosine A2a receptor antagonists.Chi B Vu et al.Bioorganic & medicinal chemistry letters, 14(19), 4835-4838 (2004-09-03) Isolation of primitive human hematopoietic progenitors on the basis of aldehyde dehydrogenase activity.R W Storms et al.Proceedings of the National Academy of Sciences of the United States of America, 96(16), 9118-9123 (1999-08-04) Microfluidic production of degradable thermoresponsive poly(N-isopropylacrylamide)-based microgels.Daryl Sivakumaran et al.Soft matter, 13(47), 9060-9070 (2017-11-28) Polymeric modification of gemcitabine via cyclic acetal linkage for enhanced anticancer potency with negligible side effects.Hiroyasu Takemoto et al.Biomaterials, 235, 119804-119804 (2020-01-29)
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