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bicyclo[3.2.0]heptan-6-one | 13756-54-2

中文名称
——
中文别名
——
英文名称
bicyclo[3.2.0]heptan-6-one
英文别名
(1RS,5RS,)-Bicyclo[3.2.0]heptan-6-one
bicyclo[3.2.0]heptan-6-one化学式
CAS
13756-54-2
化学式
C7H10O
mdl
——
分子量
110.156
InChiKey
XADFSXKNPLLSDY-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2914299000

SDS

SDS:35de12ce16753a6eac1ce292edc4b2e1
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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:
    参考文献:
    名称:
    Hine,K.E.; Childs,R.F., Canadian Journal of Chemistry, 1976, vol. 54, p. 12 - 18
    摘要:
    DOI:
  • 作为产物:
    描述:
    2-Methoxy-2-cyclohexen-1-methanol 生成 bicyclo[3.2.0]heptan-6-one
    参考文献:
    名称:
    Kirmse,W.; Alberti,J., Chemische Berichte, 1973, vol. 106, p. 236 - 245
    摘要:
    DOI:
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文献信息

  • In situ intramolecular catalytic 1,2-addition of allenoates to cyclic ketones towards polycyclic allenoates
    作者:Clément F. Heinrich、Michel Miesch、Laurence Miesch
    DOI:10.1039/c4ob02451f
    日期:——
    Sequential deprotonation, isomerization of 3-alkynoates and subsequent 1,2-addition led to bicyclic allenoate in the presence of a catalytic amount of Cs2CO3. Cyclization proceeds in a totally stereoselective manner in the case of the two-carbon linker chain. A one-pot reaction starting from alkynyl ketones afforded tricyclic fused ring systems with good yields.
    在催化量的Cs 2 CO 3存在下,连续的去质子化,3-链烷酸酯的异构化以及随后的1,2-加成导致双环烯丙酸酯。在二碳连接子链的情况下,环化以完全立体选择性的方式进行。从炔基酮开始的一锅反应得到具有良好收率的三环稠合环系统。
  • [EN] ARYLETHYNYL DERIVATIVES<br/>[FR] DÉRIVÉS D'ARYLÉTHYNYLE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2011128279A1
    公开(公告)日:2011-10-20
    The present invention relates to ethynyl derivatives of formula (I) as allosteric modulators of the metabotropic glutamate receptor subtype 5 (mGluR5). The variables in formula (I) are defined in the specification.
    本发明涉及式(I)的乙炔衍生物,作为代谢型谷氨酸受体亚型5(mGluR5)的别构调节剂。式(I)中的变量在说明书中有定义。
  • Regioselective synthesis of 1- and 4-tetralones from heteroaryl-3-cyclobutanols
    作者:Philipp Natho、Annie B. Rouse、Jake L. Greenfield、Lewis A.T. Allen、Andrew J.P. White、Zeyu Yang、Philip J. Parsons
    DOI:10.1016/j.tet.2020.131636
    日期:2020.11
    Herein we describe the first transition-metal-free ring expansion of four-membered rings to 1-tetralones from 3-substituted heteroaromatic compounds, and the first example of an oxetanol ring expansion to an oxa-tetralone. We also experimentally investigate the mechanism of the silver-mediated ring expansion and elucidate the active oxidant in these systems using electrochemical techniques.
    在本文中,我们描述了四元环从3-取代的杂芳族化合物到1-四氢萘酮的第一个无过渡金属的环扩环,以及氧杂环丁醇环扩到氧-四氢萘酮的第一个例子。我们还实验研究了银介导的扩环机理,并使用电化学技术阐明了这些系统中的活性氧化剂。
  • Preparation of 15-deoxy-16-hydroxyprostaglandins
    申请人:Miles Laboratories, Inc.
    公开号:US04132738A1
    公开(公告)日:1979-01-02
    Analogues of PGE.sub.1 having the structural formula, ##STR1## in which J is R-hydroxymethylene or S-hydroxymethylene; R.sub.1 is hydrogen; R.sub.2 is hydrogen or together with R.sub.4 is a methylene chain of 2 to 3 carbon atoms such that a cycloalkyl of 5 to 6 carbon atoms inclusive is formed; R.sub.3 is hydrogen or methyl, or together with R.sub.4 is a methylene or a lower alkylated methylene chain of 2 to 5 carbon atoms such that a cycloalkyl or a lower alkylated cycloalkyl of 4 to 7 carbon atoms inclusive is formed, or together with R.sub.4 is bicycloalkyl or bicycloalkenyl moiety having the formula: ##STR2## SUCH THAT A BICYCLOALKYL OR BICYCLOALKENYL COMPOUND IS FORMED, WHEREIN M AND N ARE INTEGERS HAVING A VALUE FROM 0 TO 3, P IS AN INTEGER HAVING A VALUE FROM 0 TO 4 AND Q IS AN INTEGER HAVING A VALUE OF FROM 1 TO 4 AND WHEREIN THE DOUBLE BOND OF SUCH BICYCLOALKENYL IS IN THE M, N, P, OR Q BRIDGE; R.sub.4 is hydrogen or methyl or together with R.sub.2 or R.sub.3 forms a cycloalkyl or bicycloalkyl or bicycloalkenyl as defined above, or together with R.sub.5 is a methylene chain of 3 to 5 carbon atoms such that a cycloalkyl of 4 to 6 carbon atoms inclusive is formed; R.sub.5 is selected from the group consisting of hydrogen, straight-chain alkyl having from 1 to 3 carbon atoms or together with R.sub.4 forms a cycloalkyl as defined above; and R.sub.6 is hydrogen or straight-chain alkyl having from 1 to 3 carbon atoms are disclosed. Pge.sub.1 ester analogues of the above formula, limited to the structures wherein two of R.sub.2, R.sub.3 R.sub.4 and R.sub.5 form a cycloalkyl, lower alkylated cycloalkyl, bicycloalkyl or bicycloalkenyl are also disclosed. The prostaglandin analogues selectively produce bronchodilation and decrease gastric secretion in vivo. Methods of preparing the analogues and starting materials required in the synthesis of the analogues are also disclosed.
    具有结构式##STR1##的PGE.sub.1的类似物,其中J是R-羟甲亚甲基或S-羟甲亚甲基;R.sub.1是氢;R.sub.2是氢或与R.sub.4一起是2到3个碳原子的亚甲基链,形成包括5到6个碳原子的环烷基;R.sub.3是氢或甲基,或与R.sub.4一起是2到5个碳原子的亚甲基或低烷基化亚甲基链,形成包括4到7个碳原子的环烷基或低烷基化环烷基,或与R.sub.4一起是具有式子的双环烷基或双环烯基基团:##STR2##形成双环烷基或双环烯基化合物,其中M和N是具有值从0到3的整数,P是具有值从0到4的整数,Q是具有值从1到4的整数,且此类双环烯基的双键位于M、N、P或Q桥上;R.sub.4是氢或甲基,或与R.sub.2或R.sub.3一起形成如上定义的环烷基或双环烷基或双环烯基,或与R.sub.5一起是3到5个碳原子的亚甲基链,形成包括4到6个碳原子的环烷基;R.sub.5选自由氢、具有1到3个碳原子的直链烷基或与R.sub.4一起形成如上定义的环烷基;R.sub.6是氢或具有1到3个碳原子的直链烷基。上述结构的Pge.sub.1酯类似物,限于其中两个R.sub.2、R.sub.3、R.sub.4和R.sub.5形成环烷基、低烷基化环烷基、双环烷基或双环烯基的结构也被披露。这些前列腺素类似物在体内选择性地产生支气管扩张并减少胃分泌。还披露了制备这些类似物以及合成这些类似物所需的起始物料的方法。
  • Regioselective Transition-Metal-Free Oxidative Cyclobutanol Ring Expansion to 4-Tetralones
    作者:Philipp Natho、Mia Kapun、Lewis A. T. Allen、Philip J. Parsons
    DOI:10.1021/acs.orglett.8b03619
    日期:2018.12.21
    A facile and transition-metal-free ring expansion of the cyclobutanol moiety to 4-tetralones fused to heteroaromatic systems is described. The oxidative ring expansion proceeds rapidly and regioselectively through mediation by N-bromosuccinimide and acetonitrile in satisfactory to good yields. The preparation of precursors and the ring expansion have proven to be scalable and are straightforward to
    描述了环丁醇部分至与杂芳族系统稠合的4-四氢萘酮的容易和无过渡金属的环膨胀。通过在N-溴代琥珀酰亚胺和乙腈的介导下,氧化环的扩环迅速且区域选择性地进行,从而令人满意地达到了良好的收率。已证明前体的制备和环的扩环是可扩展的,并且易于实施。
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