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4-(1,1,3,3-tetramethylbutyl)-2-nitrophenol | 46912-02-1

中文名称
——
中文别名
——
英文名称
4-(1,1,3,3-tetramethylbutyl)-2-nitrophenol
英文别名
Phenol, 4-tert.-octyl-2-nitro;2-nitro-4-(2,4,4-trimethylpentan-2-yl)phenol
4-(1,1,3,3-tetramethylbutyl)-2-nitrophenol化学式
CAS
46912-02-1
化学式
C14H21NO3
mdl
——
分子量
251.326
InChiKey
BHSFQPGUTBZBDA-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:
    319.6±22.0 °C(Predicted)
  • 密度:
    1.081±0.06 g/cm3(Predicted)
  • 保留指数:
    1730

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    66
  • 氢给体数:
    1
  • 氢受体数:
    3

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

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文献信息

  • A Sandwich‐Shaped Hexanuclear Silver Complex with a Giant Cavity Constructed from a Macrocycle with Inward Chelating Units
    作者:Takashi Nakamura、Rui Yun Feng、Tatsuya Nabeshima
    DOI:10.1002/ejic.202000882
    日期:2021.1.26
    The formation of a macrocyclic hexanuclear silver complex with a giant cavity (diameter ∼16.5 Å) is reported. Six silver centers are sandwiched by two molecules of a macrocyclic ligand possessing six pap (2‐[(pyridin‐2‐ylmethylene)amino]phenol) chelating units, and the metals are arranged on the wall of the internal cavity. Various analytical techniques revealed that each pap binds to the silver as
    据报道形成了具有大空腔(直径〜16.5Å)的大环六核银配合物。六个银中心被两个具有六个pap(2-[(吡啶-2--2-亚甲基)氨基]苯酚螯合单元的大环配体分子夹在中间,金属排列在内部腔壁上。各种分析技术表明,每个pap均以NN双齿配体的形式与银结合。
  • Preparation of o,o'-dihydroxyazobenzenes from o-nitrophenols
    申请人:Phillips Petroleum Company
    公开号:US04055567A1
    公开(公告)日:1977-10-25
    Compounds having the formula ##STR1## are prepared from a corresponding o-nitrophenol by blocking the hydroxyl groups via acetal formation, followed by reductive coupling and acid hydrolysis.
    具有##STR1##式的化合物是通过从相应的邻硝基苯酚开始,通过缩醛形成阻断羟基,然后进行还原偶联和酸水解制备的。
  • Preparation of high-dye yield couplers and intermediates useful therein
    申请人:EASTMAN KODAK COMPANY
    公开号:EP1016653A1
    公开(公告)日:2000-07-05
    Disclosed is a carbamyl chloride of an aminoarylcarbonyl compound having the structural formula I: wherein R is an alkyl, alkenyl, or aryl group; A is an aryl (including heteroaryl) ring group; each R' is independently an alkyl group which may form a ring with Z or Z'; p is 0, 1, 2, or 3; each Z, Z', and Y is independently hydrogen or a substituent; and n is 0, 1, or 2.
    本发明公开了一种氨基芳基羰基化合物的氨基甲酰氯,其结构式为 I: 其中 R 是烷基、烯基或芳基; A 是芳基(包括杂芳基)环基团 每个 R'独立地是一个烷基,可与 Z 或 Z'形成一个环; p 为 0、1、2 或 3; 每个 Z、Z' 和 Y 独立地是氢或取代基;以及 n 是 0、1 或 2。
  • Photographic element containing high dye-yield couplers
    申请人:EASTMAN KODAK COMPANY
    公开号:EP1016916A1
    公开(公告)日:2000-07-05
    Disclosed is a photographic element containing a light sensitive silver halide emulsion layer having associated therewith a coupler represented by Formula I: wherein COUP is a coupler parent group capable of reacting with an oxidized developer to form a first dye and is bonded at a coupling position to the group wherein X is O or NSO2R; R is an alkyl or aryl group; and DYE is a releasable second dye that is after release the same color as the first dye and is linked to OC=X by a moiety of the DYE having Formula (IA): wherein R2 is a substituent; provided there is contained in the coupler of Formula I at least one group of Formula IB: wherein L is a divalent linking group and m is 0 or 1; and Sol is a group containing an acidic hydrogen selected from the group consisting of -ArOH, -NHSO2R1 and -SO2NHR1, in which Ar is an aromatic group and each R1 is a substituent; provided further that the pKa of an acidic hydrogen of Sol is less than 8.8.
    本发明公开了一种照相元件,该元件含有感光卤化银乳剂层,并与式 I 所表示的耦合剂相关联: 其中 COUP是耦合剂母基,能与氧化显影剂反应形成第一染料,并在耦合位置与基团键合 其中 X 是 O 或 NSO2R;R 是烷基或芳基;DYE 是可释放的第二染料,释放后颜色与第一染料相同,并通过具有式 (IA) 的 DYE 分子与 OC=X 连接: 其中 R2 是取代基; 只要式 I 的耦合剂中含有至少一个式 IB 的基团: 其中 L 是二价连接基团,m 是 0 或 1;Sol 是含有酸性氢的基团,该基团选自由-ArOH、-NHSO2R1 和-SO2NHR1 组成的组,其中 Ar 是芳香基团,每个 R1 是取代基; 此外,Sol 的酸性氢的 pKa 小于 8.8。
  • Synthesis and electrode properties of 16-membered azo- and azoxycrown ethers. Structure of tribenzo-16-azocrown-6
    作者:Elżbieta Luboch、Jan F. Biernat、Yurii A. Simonov、A.A. Dvorkin
    DOI:10.1016/s0040-4020(98)00203-8
    日期:1998.5
    16-Membered benzoazo- and benzoazoxycrown ethers have been synthesized by reductive macrocyclization of respective bis(nitrophenoxy)oxaalkanes. The isomers of azocrown ethers were separated and E and Z structures were ascribed. Behavior of the compounds as ionophores in ion-selective membrane electrodes has been studied. Structure of Z isomer of 16-membered tribenzoazocrown ether has been determined. (C) 1998 Elsevier Science Ltd. All rights reserved.
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