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1-tert-butoxycarbonyloxy-4-tert-butylbenzene | 454692-73-0

中文名称
——
中文别名
——
英文名称
1-tert-butoxycarbonyloxy-4-tert-butylbenzene
英文别名
1-(tert-butoxycarbonyloxy)-4-(tert-butyl)benzene;tert-Butyl 4-tert-butylphenyl carbonate;tert-butyl (4-tert-butylphenyl) carbonate
1-tert-butoxycarbonyloxy-4-tert-butylbenzene化学式
CAS
454692-73-0
化学式
C15H22O3
mdl
——
分子量
250.338
InChiKey
PCACHSHNFNYLRI-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:
    318.2±25.0 °C(Predicted)
  • 密度:
    1.002±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.7
  • 重原子数:
    18
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1-tert-butoxycarbonyloxy-4-tert-butylbenzene哌啶 作用下, 以 二氯甲烷 为溶剂, 反应 10.0h, 以93%的产率得到4-叔丁基苯酚
    参考文献:
    名称:
    Base-labile tert-butoxycarbonyl (Boc) group on phenols
    摘要:
    Phenols are deprotected with weak bases from their tert-butoxycarbonyl (Boc) derivatives. Boc deprotection with bases can avoid side reactions during the deprotection with acids. We note the lability of the Boc to bases and are able to utilize it as a new cleavage condition for synthetic studies. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2003.11.008
  • 作为产物:
    参考文献:
    名称:
    Optically active compound and photosensitive resin composition
    摘要:
    一种光活性化合物与光敏剂结合使用,由以下公式(1)表示: A −[( J ) m −( X-Pro )] n (1) 其中,A代表至少包括一种从烃基和杂环基中选择的疏水基的疏水单元,J代表连接基团,X-Pro代表由光照可去除的保护基团Pro保护的亲水基团,m代表0或1,n代表不少于1的整数。 保护基团Pro可以与光敏剂(特别是光酸发生剂)一起通过光照可去除,也可以是疏水保护基团。亲水基团可以是羟基或羧基。光活性化合物对短波长光源具有很高的敏感性,用于光刻应用,因此,该光活性化合物有利于形成具有高分辨率的图案。
    公开号:
    US20030211421A1
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文献信息

  • Optically active compound and photosensitive resin composition
    申请人:——
    公开号:US20030211421A1
    公开(公告)日:2003-11-13
    A photoactive compound is used in combination with a photosensitizer, represented by the following formula (1): A −[( J ) m −( X-Pro )] n (1) wherein A represents a hydrophobic unit comprising at least one kind of hydrophobic groups selected from a hydrocarbon group and a heterocyclic group, J represents a connecting group, X-Pro represents a hydrophilic group protected by a protective group Pro which is removable by light exposure, m represents 0 or 1, and n represents an integer of not less than 1. The protective group Pro may be removable by light exposure in association with the photosensitizer (especially, a photo acid generator), or may be a hydrophobic protective group. The hydrophilic group may be a hydroxyl group or a carboxyl group. The photoactive compound has high sensitivity to a light source of short wavelength beams, for resist application, therefore, the photoactive compound is advantageously used for forming a pattern with high resolution.
    一种光活性化合物与光敏剂结合使用,由以下公式(1)表示: A −[( J ) m −( X-Pro )] n (1) 其中,A代表至少包括一种从烃基和杂环基中选择的疏水基的疏水单元,J代表连接基团,X-Pro代表由光照可去除的保护基团Pro保护的亲水基团,m代表0或1,n代表不少于1的整数。 保护基团Pro可以与光敏剂(特别是光酸发生剂)一起通过光照可去除,也可以是疏水保护基团。亲水基团可以是羟基或羧基。光活性化合物对短波长光源具有很高的敏感性,用于光刻应用,因此,该光活性化合物有利于形成具有高分辨率的图案。
  • Protein-Polymer-Drug Conjugates
    申请人:Yurkovetskiy Aleksandr
    公开号:US20120321583A1
    公开(公告)日:2012-12-20
    A drug conjugate is provided herein. The conjugate comprises a protein based recognition-molecule (PBRM) and a polymeric carrier substituted with one or more -L D -D, the protein based recognition-molecule being connected to the polymeric carrier by L P . Each occurrence of D is independently a therapeutic agent having a molecular weight ≦5 kDa. L D and L P are linkers connecting the therapeutic agent and PBRM to the polymeric carrier respectively. Also disclosed are polymeric scaffolds useful for conjugating with a PBRM to form a polymer-drug-PBRM conjugate described herein, compositions comprising the conjugates, methods of their preparation, and methods of treating various disorders with the conjugates or their compositions.
    本文提供了一种药物结合物。该结合物包括一种基于蛋白质的识别分子(PBRM)和一个聚合物载体,该载体被一个或多个-LD-D取代,基于蛋白质的识别分子通过LP连接到聚合物载体上。每个D的出现都是分子量≦5 kDa的治疗剂。LD和LP是连接治疗剂和PBRM到聚合物载体的连接剂。还公开了用于与PBRM结合形成聚合物-药物-PBRM结合物的聚合物支架,包括结合物的组成,其制备方法以及使用结合物或其组成物治疗各种疾病的方法。
  • Auristatin Compounds and Conjugates Thereof
    申请人:Mersana Therapeutics, Inc.
    公开号:US20130309192A1
    公开(公告)日:2013-11-21
    Auristatin compounds and conjugates thereof are provided herein. The conjugate comprises a protein based recognition-molecule (PBRM) and a polymeric carrier substituted with one or more -L D -D, the protein based recognition-molecule being connected to the polymeric carrier by L P . Each occurrence of D is independently an Auristatin compound. L D and L P are linkers connecting the therapeutic agent and PBRM to the polymeric carrier respectively. Also disclosed are polymeric scaffolds useful for conjugating with a PBRM to form a polymer-drug-PBRM conjugate described herein, compositions comprising the conjugates, methods of their preparation, and methods of treating various disorders with the conjugates or their compositions.
    本文提供了Auristatin化合物及其共轭物。该共轭物包括基于蛋白质识别分子(PBRM)的识别分子和被取代一个或多个-LD-D的聚合物载体,其中蛋白质识别分子通过LP连接到聚合物载体上。每个D的出现都是独立的Auristatin化合物。LD和LP是连接治疗剂和PBRM到聚合物载体的连接剂。本文还揭示了用于与PBRM共轭形成聚合物-药物-PBRM共轭物的聚合物支架,包括所述共轭物的组成,其制备方法以及使用共轭物或其组成治疗各种疾病的方法。
  • PROTEIN-POLYMER-DRUG CONJUGATES
    申请人:MERSANA THERAPEUTICS, INC.
    公开号:US20150044160A1
    公开(公告)日:2015-02-12
    A drug conjugate is provided herein. The conjugate comprises a protein based recognition-molecule (PBRM) and a polymeric carrier substituted with one or more -L D -D, the protein based recognition-molecule being connected to the polymeric carrier by L P . Each occurrence of D is independently a therapeutic agent having a molecular weight ≦5 kDa. L D and L P are linkers connecting the therapeutic agent and PBRM to the polymeric carrier respectively. Also disclosed are polymeric scaffolds useful for conjugating with a PBRM to form a polymer-drug-PBRM conjugate described herein, compositions comprising the conjugates, methods of their preparation, and methods of treating various disorders with the conjugates or their compositions.
    本文提供一种药物偶联物。该偶联物包括一种基于蛋白质的识别分子(PBRM)和一种聚合物载体,其取代了一个或多个-LD-D,其中,基于蛋白质的识别分子通过LP连接到聚合物载体上。每个D的出现都是独立的,其分子量≦5 kDa,是一种治疗剂。LD和LP是连接治疗剂和PBRM到聚合物载体的连接体。还公开了用于与PBRM偶联形成聚合物-药物-PBRM偶联物的聚合物支架,包括所述偶联物的组合物,其制备方法以及使用偶联物或其组合物治疗各种疾病的方法。
  • Terminally Modified Polymers and Conjugates Thereof
    申请人:Mersana Therapeutics, Inc.
    公开号:US20140017265A1
    公开(公告)日:2014-01-16
    A terminally modified polymer is provided herein. At least one terminus of the polymer is —O—(CH 2 ) 2 -L M or —O—CH 2 —CH(OH)—CH 2 —CR 1 ═CR 2 R 3 . L M , R 1 , R 2 , and R 3 are defined herein Also disclosed are terminal conjugates comprising the polymer and a pharmaceutically useful modifier, as well as compositions comprising the conjugates, methods of their preparation, and methods of treating various disorders with the conjugates or their compositions.
    本文提供了一种终止修饰的聚合物。聚合物的至少一个端点是—O—(CH2)2-LM或—O—CH2—CH(OH)—CH2—CR1═CR2R3。其中LM,R1,R2和R3在本文中有定义。此外,本文还披露了包括该聚合物和药物有用修饰剂的终端共轭物,以及包括共轭物的组合物、其制备方法以及使用共轭物或其组合物治疗各种疾病的方法。
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