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1-溴-2-(溴二氟甲基)环己烷 | 14737-09-8

中文名称
1-溴-2-(溴二氟甲基)环己烷
中文别名
——
英文名称
cis/trans-1-bromodifluoromethyl-2-bromocyclohexane
英文别名
2-bromo-1-bromodifluoromethylcyclohexane;1-Bromo-2-(bromodifluoromethyl)cyclohexane;1-bromo-2-[bromo(difluoro)methyl]cyclohexane
1-溴-2-(溴二氟甲基)环己烷化学式
CAS
14737-09-8
化学式
C7H10Br2F2
mdl
——
分子量
291.961
InChiKey
MWCUYVZBWZWWKO-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    108 °C
  • 密度:
    1.806±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 危险品标志:
    Xi
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2903890090
  • 安全说明:
    S26,S36

SDS

SDS:d0c2a6259b5689fa325a82c5892aadd1
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-溴-2-(溴二氟甲基)环己烷 作用下, 以 乙醚 为溶剂, 以19%的产率得到7,7-difluoronorcarane
    参考文献:
    名称:
    Mechanistic Studies on Zinc-Induced Addition of CF2Br2 to Olefins. A Novel Radical Reductive Cyclopropanation on the Zinc Surface
    摘要:
    The addition reaction of dibromodifluoromethane (1) to olefins induced by zinc in ethereal solvent differs surprisingly from addition reactions hitherto reported. Both cyclopropane derivatives and 1:1 addition products were obtained from this reaction. A free-radical chain addition reaction induced ; by single electron transfer (SET) is proposed. This reaction is inhibited by hydroquinone and completely quenched by p-dinitrobenzene. The nature of the 1:1 adducts formed revealed the character of a typical radical reaction. The nature of the cyclopropane derivatives formed was also much different from the usual cyclopropane adduct derived from carbene addition. When diallyl ether (15) and norbornadiene (16) were used as substrates, only rearranged 1:1 addition products could be obtained, and no cyclopropane product could be detected. The results of addition reactions with 4-octenes (27) showed also that the cyclopropanation reaction was not stereospecific. On the basis of the above-mentioned results, a novel reductive debromocyclopropanation reaction of the gamma-bromopropyl radical intermediate proceeding on the zinc metal surface is suggested.
    DOI:
    10.1021/jo00083a030
  • 作为产物:
    描述:
    二溴二氟甲烷环己烯 在 chromium chloride 、 铁粉 作用下, 以 乙醇 为溶剂, 反应 10.0h, 生成 1-溴-2-(溴二氟甲基)环己烷
    参考文献:
    名称:
    Synthesis of bromodifluoromethyl-substituted alkenes. Potassium fluoride supported on alumina as a dehydrobrominating agent
    摘要:
    Potassium fluoride supported on alumina is an efficient dehydrobrominating agent. 1,3-Dibromo-1,1-difluoroalkanes - adducts of dibromodifluoromethane and alkenes - give bromodifluoromethyl-substituted alkenes 2 on dehydrobromination with this agent in good to excellent yields. Alkenes 2 were a mixture of Z- and E-isomers, with the former predominating. Functional groups such as ester, carbonyl, ethylenic and chloromethyl are not affected under such reaction conditions.
    DOI:
    10.1016/0022-1139(93)02954-d
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文献信息

  • A convenient synthesis of bromodifluoromethyl-substituted alkenes
    作者:Chang-Ming Hu、Jian Chen
    DOI:10.1016/0022-1139(93)03051-m
    日期:1994.10
    Various functionalized bromodifluoromethyl-substituted alkenes have been prepared by addition of dibromodifluoromethane to functionalized alkenes promoted by a CrCl3/Fe bimetal redox system, followed by dehydrobromination with KF/Al2O3.
  • Difluoromethylation of alkenes via borohydride reduction of 1,3-dibromo-1,1-difluoroalkanes
    作者:Javier Gonzalez、Christopher J. Foti、Seth Elsheimer
    DOI:10.1021/jo00013a051
    日期:1991.6
  • Unexpected products from the reactions of 1-(bromodifluoromethyl)-2-bromocyclohexanes with potassium hydroxide
    作者:Seth Elsheimer、Mariana Michael、Antonio Landavazo、Darlene K. Slattery、Jennifer Weeks
    DOI:10.1021/jo00261a041
    日期:1988.12
  • GONZALEZ, JAVIER;FOTI, CHRISTOPHER J.;ELSHEIMER, SETH, J. ORG. CHEM., 56,(1991) N3, C. 4322-4325
    作者:GONZALEZ, JAVIER、FOTI, CHRISTOPHER J.、ELSHEIMER, SETH
    DOI:——
    日期:——
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同类化合物

顺式-2-氯环己基高氯酸盐 顺式-1-溴-2-氟-环己烷 顺式-1-叔丁基-4-氯环己烷 顺式-1,2-二氯环己烷 顺-1H,4H-十二氟环庚烷 镓,三(三氟甲基)- 镁二(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-十七氟-1-辛烷磺酸酯) 铵2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-二十三氟十二烷酸盐 铜N-(2-氨基乙基)乙烷-1,2-二胺2-氰基胍二氯化盐酸 钾{[(十七氟辛基)磺酰基](甲基)氨基}乙酸酯 钠3-[(3-{[(十七氟辛基)磺酰基]氨基}丙基)(甲基)氨基]-1-丙烷磺酸酯 重氮基烯,(1-溴环己基)(1,1-二甲基乙基)-,1-氧化 辛酸,十五氟-,2-(1-羰基辛基)酰肼 赖氨酰-精氨酰-精氨酰-苯基丙氨酰-赖氨酰-赖氨酸 诱蝇羧酯B1 诱蝇羧酯 萘并[2,1-b]噻吩-1(2H)-酮 膦基硫杂酰胺,P,P-二(三氟甲基)- 脲,N-(4,5-二甲基-4H-吡唑-3-基)- 肼,(3-环戊基丙基)-,盐酸(1:1) 组织蛋白酶R 磷亚胺三氯化,(三氯甲基)- 碳标记全氟辛酸 碘甲烷与1-氮杂双环(4.2.0)辛烷高聚合物的化合物 碘甲烷-d2 碘甲烷-d1 碘甲烷-13C,d3 碘甲烷 碘环己烷 碘仿-d 碘仿 碘乙烷-D1 碘[三(三氟甲基)]锗烷 硫氰酸三氯甲基酯 甲烷,三氯氟-,水合物 甲次磺酰胺,N,N-二乙基-1,1,1-三氟- 甲次磺酰氯,氯二[(三氟甲基)硫代]- 甲基碘-12C 甲基溴-D1 甲基十一氟环己烷 甲基丙烯酸正乙基全氟辛烷磺 甲基三(三氟甲基)锗烷 甲基[二(三氟甲基)]磷烷 甲基1-氟环己甲酸酯 环戊-1-烯-1-基全氟丁烷-1-磺酸酯 环己烷甲酸4,4-二氟-1-羟基乙酯 环己烷,1-氟-2-碘-1-甲基-,(1R,2R)-rel- 环己基五氟丙烷酸酯 环己基(1-氟环己基)甲酮 烯丙基十七氟壬酸酯