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2-Methylidenecyclohexane-1,3-dione | 104824-58-0

中文名称
——
中文别名
——
英文名称
2-Methylidenecyclohexane-1,3-dione
英文别名
——
2-Methylidenecyclohexane-1,3-dione化学式
CAS
104824-58-0
化学式
C7H8O2
mdl
——
分子量
124.14
InChiKey
KURCYEGRZOENBR-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):
    0.6
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • METHOD OF PRODUCING A BISBENZODITHIOL COMPOUND
    申请人:Motoki Masuji
    公开号:US20090240067A1
    公开(公告)日:2009-09-24
    A method of producing a compound represented by formula (1), including: allowing 1,4-benzoquinone or 1,2-benzoquinone to react with a dithiocarbamate compound represented by formula (2) in a polar solvent: wherein R 1 and R 2 each independently represent a hydrogen atom, an alkyl group, an aryl group or a heterocyclic group, R 1 and R 2 may be the same or different and may be combined with each other to form a ring, X represents an ion necessary to neutralize the charge of the molecule, m represents an integer of 1 to 2, n represents an integer of 1 to 2, M represents a hydrogen atom, a metal atom or a conjugate acid of a base, p represents an integer of 1 to 4, and q represents an integer of 1 to 4.
    一种生产由化学式(1)表示的化合物的方法,包括:允许1,4-苯醌或1,2-苯醌在极性溶剂中与由化学式(2)表示的二硫代氨基甲酸盐化合物发生反应:其中R1和R2各自独立地表示氢原子、烷基、芳基或杂环基,R1和R2可以相同也可以不同,并且可以结合在一起形成环,X表示中性化分子电荷所需的离子,m表示1至2的整数,n表示1至2的整数,M表示氢原子、金属原子或碱的共轭酸,p表示1至4的整数,q表示1至4的整数。
  • METHOD FOR COUPLING MOLECULES
    申请人:MEDICAL RESEARCH COUNCIL
    公开号:EP1207909A2
    公开(公告)日:2002-05-29
  • TWO-PHOTON OR HIGHER-ORDER ABSORBING OPTICAL MATERIALS FOR GENERATION OF REACTIVE SPECIES
    申请人:Cumpston Brian
    公开号:US20080283804A1
    公开(公告)日:2008-11-20
    Disclosed are highly efficient multiphoton absorbing compounds and methods of their use. The compounds generally include a bridge of pi-conjugated bonds connecting electron donating groups or electron accepting groups. The bridge may be substituted with a variety of substituents as well. Solubility, lipophilicity, absorption maxima and other characteristics of the compounds may be tailored by changing the electron donating groups or electron accepting groups, the substituents attached to or the length of the pi-conjugated bridge. Numerous photophysical and photochemical methods are enabled by converting these compounds to electronically excited states upon simultaneous absorption of at least two photons of radiation. The compounds have large two-photon or higher-order absorptivities such that upon absorption, one or more Lewis acidic species, Lewis basic species, radical species or ionic species are formed.
  • OPTICAL RECORDING MEDIUM AND METHOD OF RECORDING VISIBLE INFORMATION
    申请人:SETO Nobuo
    公开号:US20090022047A1
    公开(公告)日:2009-01-22
    The optical recording medium comprises a visible information recording layer comprising at least two dyes of the following dyes. R a1 to R b3 each independently denote a hydrogen atom or a monovalent substituent, R a2 and R a3 may bond together to form a five to seven-membered heterocyclic ring, A denotes a substituted or unsubstituted aliphatic group, substituted or unsubstituted aryl group, or substituted or unsubstituted heterocyclic group, n denotes 0, 1, 2, or 3. Za 21 and Za 22 each independently denote an atom group forming an acidic nucleus, Ma 21 to Ma 23 each independently denote a substituted or unsubstituted methine group, Ka 21 denotes an integer ranging from 0 to 3, and Q denotes a monovalent cation. A 1 =N—B 1 General formula (III) A 1 denotes a substituted or unsubstituted heterocyclic group, a substituted aliphatic group, or a substituted or unsubstituted carbocyclic group, and B 1 denotes a substituted or unsubstituted heterocyclic group or a substituted or unsubstituted aryl group.
  • ULTRAVIOLET ABSORBENT COMPOSITION
    申请人:Hanaki Naoyuki
    公开号:US20100025642A1
    公开(公告)日:2010-02-04
    An ultraviolet absorbent composition, containing: at least one kind of ultraviolet absorbent A having an absorption maximum wavelength of from 350 nm to 400 nm, a half value width of 55 nm or less and a molar extinction coefficient of 20,000 or more at the absorption maximum wavelength; and at least one kind of ultraviolet absorbent B having an absorption maximum wavelength of 350 nm or less and showing 30% or more of absorbance at 320 nm of the absorbance at the absorption maximum wavelength.
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