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2-methyl-4-(tert-pentyl)phenol | 71745-63-6

中文名称
——
中文别名
——
英文名称
2-methyl-4-(tert-pentyl)phenol
英文别名
2-Methyl-4-(2-methylbutan-2-yl)phenol
2-methyl-4-(tert-pentyl)phenol化学式
CAS
71745-63-6
化学式
C12H18O
mdl
——
分子量
178.274
InChiKey
BTNRRXSBIPTRIQ-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

  • 熔点:
    15°C
  • 沸点:
    260.36°C (estimate)
  • 密度:
    0.9690

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:3836d592df17d64f7d673b8339f7beec
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上下游信息

  • 上游原料
    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:
    2-methyl-4-(tert-pentyl)phenol 作用下, 生成 2-chloro-6-methyl-4-tert-pentyl-phenol
    参考文献:
    名称:
    Halo-substituted polyalkyl phenols
    摘要:
    公开号:
    US02221808A1
  • 作为产物:
    描述:
    对叔戊基苯酚 、 palladium diacetate 、 potassium carbonate 作用下, 以 二氯甲烷甲苯 为溶剂, 反应 32.5h, 生成 2-methyl-4-(tert-pentyl)phenol
    参考文献:
    名称:
    [EN] MACROCYCLIC BROAD SPECTRUM ANTIBIOTICS
    [FR] ANTIBIOTIQUES MACROCYCLIQUES À LARGE SPECTRE
    摘要:
    本文提供了抗菌化合物,其中在某些实施例中,这些化合物具有广谱生物活性。在各种实施例中,这些化合物通过抑制细菌类型1信号肽酶(SpsB)发挥作用,这是细菌中的一种必需蛋白质。还提供了使用所述化合物的药物组合物和治疗方法。
    公开号:
    WO2017084630A1
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文献信息

  • Total Synthesis of Pyrolaside B: Phenol Trimerization through Sequenced Oxidative C−C and C−O Coupling
    作者:William C. Neuhaus、Marisa C. Kozlowski
    DOI:10.1002/anie.201915654
    日期:2020.5.11
    A facile method to oxidatively trimerize phenols using a catalytic aerobic copper system is described. The mechanism of this transformation was probed, yielding insight that enabled cross-coupling trimerizations. With this method, the natural product pyrolaside B was synthesized for the first time. The key strategy used for this novel synthesis is the facile one-step construction of a spiroketal trimer
    描述了一种使用催化需氧铜系统氧化三聚苯酚的简便方法。对这种转化的机制进行了探讨,获得了实现交叉偶联三聚化的见解。利用该方法首次合成了天然产物马焦拉苷B。这种新颖合成所采用的关键策略是轻松一步构建螺缩酮三聚体中间体,该中间体可以选择性还原以得到天然产物框架,而无需求助于逐步的乌尔曼型和铃木型偶联。结果,经过五步即可快速获得吡咯苷B,总收率为16%。合成了其他三种类似物,从而突出了该方法的实用性,为该化学空间领域提供了新的途径。还通过受控路易斯酸促进螺缩酮三聚体的重排合成了一种新型呫吨。
  • ORGANIC DYE COMPOUND AND HIGH DENSITY OPTICAL RECORDING MEDIUM INCLUDING THE SAME
    申请人:Wang Shin-Shin
    公开号:US20100047509A1
    公开(公告)日:2010-02-25
    A recording layer including a novel organic dye compound (I) for a high density optical recording medium is provided. The organic dye compound (I) has the following general chemical structural formula: wherein R 1 , R 2 , R 3 , R 4 and R 5 each independently represent H, alkyl, halide, nitro, benzyl group or substituted benzyl group. The organic dye compound (I) exhibits a maximum absorbance at a wavelength range of 400-550 nm.
    提供一种包括新型有机染料化合物(I)的记录层,用于高密度光学记录介质。有机染料化合物(I)具有以下一般化学结构式:其中R1、R2、R3、R4和R5各自独立地表示H、烷基、卤素、硝基、苄基或取代苄基。有机染料化合物(I)在400-550 nm波长范围内表现出最大吸收。
  • MEDICAMENT FOR TREATMENT OF NEURODEGENERATIVE DISEASES
    申请人:MUTO Susumu
    公开号:US20080234233A1
    公开(公告)日:2008-09-25
    A medicament for preventive and/or therapeutic treatment of neurodegenerative diseases such as Alzheimer's disease or the like which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: wherein A represents hydrogen atom or acetyl group, E represents a 2,5-di-substituted or a 3,5-di-substituted phenyl group, or a monocyclic or a fused polycyclic heteroaryl group which may be substituted, provided that the compound wherein said heteroaryl group is circle around (1)} a fused polycyclic heteroaryl group wherein the ring which binds directly to —CONH— group in the formula (I) is a benzene ring, circle around (2)} unsubstituted thiazol-2-yl group, or circle around (3)} unsubstituted benzothiazol-2-yl group is excluded, ring Z represents an arene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —CONH-E wherein E has the same meaning as that defined above, or a heteroarene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —CONH-E wherein E has the same meaning as that defined above.
    这是一种用于预防和/或治疗神经退行性疾病,如阿尔茨海默病等的药物,其包括以下通式(I)所表示的化合物中所选的一种作为活性成分,以及其药学上可接受的盐、水合物和溶剂化合物:其中,A代表氢原子或乙酰基,E代表2,5-二取代或3,5-二取代苯基,或单环或融合的多环杂环芳基,可以取代,但是当所述杂环芳基为圆圈1}在公式(I)中直接结合—CONH—基团的环为苯环,圆圈2}未取代的噻唑-2-基团,或圆圈3}未取代的苯并噻唑-2-基团时,排除在外,环Z代表一个芳烃,除了由公式—O-A所表示的基团和由公式—CONH-E所表示的基团外,还可以有一个或多个取代基,其中A具有上述定义的相同含义,E具有上述定义的相同含义,或者代表一个杂芳烃,除了由公式—O-A所表示的基团和由公式—CONH-E所表示的基团外,还可以有一个或多个取代基。
  • ANTIALLERGIC AGENTS
    申请人:Muto Susumu
    公开号:US20080090779A1
    公开(公告)日:2008-04-17
    A medicament for the preventive and/or therapeutic treatment of allergic diseases and/or endometriosis and/or hysteromyoma which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: wherein X represents a connecting group whose number of atoms in the main chain is 2 to 5 (said connecting group may be substituted), A represents hydrogen atom or acetyl group, E represents an aryl group which may be substituted or a hetero aryl group which may be substituted, ring Z represents an arene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above, or a heteroarene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above.
    一种预防和/或治疗过敏性疾病和/或子宫内膜异位症和/或子宫肌瘤的药物,其包括以下通式(I)所表示的化合物或其药学上可接受的盐、水合物和溶剂化物作为活性成分,其中X表示连接基,其主链中原子数为2至5(该连接基可以被取代),A表示氢原子或乙酰基,E表示芳基或取代的杂芳基,环Z表示苯环,除了由公式-O-A表示的基团,该苯环还可以具有一个或多个取代基团,其中A的含义与上述定义相同,而由公式-X-E表示的基团中,每个X和E的含义也与上述定义相同,或者是一个杂环,除了由公式-O-A表示的基团,该杂环还可以具有一个或多个取代基团,其中A的含义与上述定义相同,而由公式-X-E表示的基团中,每个X和E的含义也与上述定义相同。
  • Antiallergic agents
    申请人:Muto Susumu
    公开号:US20070185059A1
    公开(公告)日:2007-08-09
    A medicament for the preventive and/or therapeutic treatment of allergic diseases and/or endometriosis and/or hysteromyoma which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: wherein X represents a connecting group whose number of atoms in the main chain is 2 to (said connecting group may be substituted), A represents hydrogen atom or acetyl group, E represents an aryl group which may be substituted or a hetero aryl group which may be substituted, ring Z represents an arene which may have one or more substitutents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above, or a heteroarene which may have one or more substitutents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above.
    一种用于预防和/或治疗过敏性疾病和/或子宫内膜异位症和/或子宫肌瘤的药物,其活性成分包括以下通式(I)表示的化合物或其药学上可接受的盐、水合物和溶剂化物中的一种,其中X代表连接基,其主链中的原子数为2到(该连接基可以被取代),A代表氢原子或乙酰基,E代表芳基或取代的杂环芳基,环Z代表芳烃,除了由公式-O-A表示的基团外,还可以有一个或多个取代基,其中A具有上述定义的相同含义,并且由公式-X-E表示的基团,其中X和E的每个都具有上述定义的相同含义,或者可以有一个或多个取代基的杂芳烃,其中A具有上述定义的相同含义,并且由公式-X-E表示的基团,其中X和E的每个都具有上述定义的相同含义。
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