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perezinone | 10124-08-0

中文名称
——
中文别名
——
英文名称
perezinone
英文别名
(5R)-6-hydroxy-2,2,5,8-tetramethyl-4,5-dihydro-2H,3H-naphtho[1,8-bc]furan-7-one;(5R)-6-Hydroxy-2,2,5,8-tetramethyl-4,5-dihydro-2H,3H-naphtho[1,8-bc]furan-7-on;Perezinon;(R)-4,5-Dihydro-6-hydroxy-2,2,5,8-tetramethyl-2H-naphtho[1,8-bc]furan-7(3H)-one;(7R)-9-hydroxy-3,3,7,11-tetramethyl-2-oxatricyclo[6.3.1.04,12]dodeca-1(11),4(12),8-trien-10-one
perezinone化学式
CAS
10124-08-0
化学式
C15H18O3
mdl
——
分子量
246.306
InChiKey
GPLYVANRJRWDMO-SSDOTTSWSA-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

  • 熔点:
    166-167 °C
  • 沸点:
    424.4±45.0 °C(Predicted)
  • 密度:
    1.22±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

SDS

SDS:7a0be4d78e345cd631ea3268b0c7fcb6
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反应信息

  • 作为产物:
    描述:
    羟基三褶菊酮三氟化硼乙醚 作用下, 以 二氯甲烷 为溶剂, 以66%的产率得到perezinone
    参考文献:
    名称:
    Boron trifluoride-catalyzed cycloadditions of naturally occurring sesquiterpene p-benzoquinones
    摘要:
    DOI:
    10.1021/jo00381a010
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文献信息

  • Inhibition of polymerization of unsaturated monomers
    申请人:——
    公开号:US20020037958A1
    公开(公告)日:2002-03-28
    Disclosed herein is a method for inhibiting the premature polymerization of ethylenically unsaturated monomers comprising adding to said monomers an effective amount of a mixture comprising: A) at least one stable hindered nitroxyl compound having the structural formula: 1 wherein R 1 and R 4 are independently selected from the group consisting of hydrogen, alkyl, and heteroatom-substituted alkyl and R 2 and R 3 are independently selected from the group consisting of alkyl and heteroatom-substituted alkyl; and X 1 and X 2 (1) are independently selected from the group consisting of halogen, cyano, COOR 7 , —S—COR 7 , —OCOR 7 , (wherein R 7 is alkyl or aryl), amido, —S—C 6 H 5 , carbonyl, alkenyl, or alkyl of 1 to 15 carbon atoms, or (2) taken together, form a ring structure with the nitrogen; and B) at least one inhibitor selected from the group consisting of ortho-quinone, ortho-hydroquinone, para-quinone, para-hydroquinone, and derivatives of the foregoing.
    本文公开了一种抑制乙烯基不饱和单体过早聚合的方法,包括向所述单体中加入有效量的混合物,该混合物包括 A) 至少一种具有结构式的稳定受阻硝基化合物: 1 其中 R 1 和 R 4 独立地选自氢、烷基、杂原子取代的烷基和 R 2 和 R 3 独立地选自由烷基和杂原子取代的烷基组成的组;以及 X 1 和 X 2 (1)独立地选自由卤素、氰基、COR 7 、-S-COR 7 、-OCOR 7 ,(其中 R 7 为烷基或芳基)、氨基、-S-C 6 H 5 1至15个碳原子的羰基、烯基或烷基,或(2)合在一起与氮形成环状结构;以及 B) 至少一种选自邻醌、邻氢醌、对苯醌、对氢醌和上述物质的衍生物的抑制剂。
  • The structure of β-isopipitzol
    作者:Francisco Yuste、Héctor Barrios、Eduardo Díaz、Benjamín Ortiz、Rubén Sánchez-Obregón、Fernando Walls
    DOI:10.1016/s0040-4039(00)78534-0
    日期:1994.12
    The Lewis acid catalyzed intramolecular cycloaddition of isoperezone (5) produced a tricyclic compound containing a new skeleton named beta-isopipitzol (6), perezinone (7) and dihydroisoperezinone (8).
  • INHIBITION OF POLYMERIZATION OF UNSATURATED MONOMERS
    申请人:CROMPTON CORPORATION
    公开号:EP1233937B1
    公开(公告)日:2005-10-26
  • US6653414B2
    申请人:——
    公开号:US6653414B2
    公开(公告)日:2003-11-25
  • [EN] INHIBITION OF POLYMERIZATION OF UNSATURATED MONOMERS<br/>[FR] INHIBITION DE POLYMERISATION DE MONOMERES INSATURES
    申请人:CROMPTON CORP
    公开号:WO2001040149A2
    公开(公告)日:2001-06-07
    Disclosed herein is a method for inhibiting the premature polymerization of ethylenically unsaturated monomers comprising adding to said monomers an effective amount of a mixture comprising: A) at least one stable hindered nitroxyl compound having structural formula (I) wherein R1 and R4 are independently selected from the group consisting of hydrogen, alkyl, and heteroatom-substituted alkyl and R2 and R3 are independently selected from the group consisting of alkyl and heteroatom-substituted alkyl; and X1 and X2 (1) are independently selected from the group consisting of halogen, cyano, COOR7, -S-COR7, -OCOR7, (wherein R7 is alkyl or aryl), amido, -S-C6H5, carbonyl, alkenyl, or alkyl of 1 to 15 carbon atoms, or (2) taken together, form a ring structure with the nitrogen; and B) at least one inhibitor selected from the group consisting of ortho-quinone, ortho-hydroquinone, para-quinone, para-hydroquinone, and derivatives of the foregoing.
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