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12H-苯并[a]吩噻嗪 | 225-83-2

中文名称
12H-苯并[a]吩噻嗪
中文别名
——
英文名称
benzophenothiazine
英文别名
12H-benzo(α)phenothiazine;12H-benzo[α]phenothiazine;12H-benzo[a]phenothiazine;benzo[a]phenothiazine;M627;12H-benzo[a]phenothiazine
12H-苯并[a]吩噻嗪化学式
CAS
225-83-2
化学式
C16H11NS
mdl
——
分子量
249.336
InChiKey
PGIGZWJIJSINOD-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:
    136-137 °C
  • 沸点:
    467.7±15.0 °C(Predicted)
  • 密度:
    1.274±0.06 g/cm3(Predicted)
  • 溶解度:
    1.27e-06 M

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2934999090

SDS

SDS:f41557ffda2a5d21b556dbf2014f16fe
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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

  • 作为反应物:
    描述:
    12H-苯并[a]吩噻嗪溶剂黄146 作用下, 反应 12.0h, 以66.9%的产率得到
    参考文献:
    名称:
    一种含有芴的有机化合物及其制备方法和在有机电致发光器件上应用
    摘要:
    本发明公开了一种含有芴的有机化合物,该有机化合物的结构式通式如通式(1)所示。本发明化合物具有较高的玻璃化温度和分子热稳定性,合适的HOMO和LUMO能级,较高Eg,通过器件结构优化,可有效提升OLED器件的光电性能以及OLED器件的寿命。
    公开号:
    CN107868051A
  • 作为产物:
    描述:
    N-苯基-1-萘胺 、 sulfur 作用下, 以 邻二氯苯 为溶剂, 反应 4.0h, 生成 12H-苯并[a]吩噻嗪
    参考文献:
    名称:
    吩噻嗪范围:立体应变诱导的平面化和准分子形成。
    摘要:
    基于10-苯基-10H-吩噻嗪(NAS)发色团的吩噻嗪衍生物,即7-苯基-7H-苯并[c]吩噻嗪(NAS-1)和12-苯基-12H-苯并[a]吩噻嗪(NAS-2) ),进行了设计和合成。NAS-1和NAS-2是对吩噻嗪核心部分施加不同空间应变的结构异构体。在解决方案中,应变更大的NAS-2拥有弯曲的结构,并经历了光致结构平面化(PISP)。在晶体中,尽管没有PISP,弯曲的NAS-2仍表现出显着的准分子发射以及发射机械变色现象,而在平面状NAS和NAS-1中则没有观察到。这种非常规的观察结果是由于弯曲的核结构促进了周围萘部分的π-π堆积。
    DOI:
    10.1002/anie.201906083
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文献信息

  • PHOTOSENSITIZER AND DERIVATIVES AND APPLICATION THEREOF
    申请人:DALIAN UNIVERSITY OF TECHNOLOGY
    公开号:US20210030873A1
    公开(公告)日:2021-02-04
    A photosensitizer and derivative, application thereof. The photosensitizer has the structure of general formula I, wherein X is S or Se, Y is organic or inorganic ion, R 1 and R 2 are independently selected from H, alkyl, alkoxy, alkyl amido, alkyl azide and the like; R 3 is selected from H, alkyl, alkoxy, amino sulfonyl, hydroxyl, carboxyl and the like, and L 1 is a linker selected from —(CH 2 ) n1 — or —(CH 2 CH 2 O) n2 —. The derivatives are molecular medicines with drug molecules of anticancer and chemotherapy or tumor targeting function connected to the said photosensitizer. The photosensitizer has excellent near infrared characteristics and low dark toxicity and is used in the field of photodynamic tumor therapy. The introduction of benzophenothiazine or benzophenoselenazine into derivatives with tumor-targeting function could improve the specific uptake of photosensitizer in tumor tissues. Moreover, clinical anticancer drugs can be introduced into the structure of benzophenothiazine or benzophenoselenazine to achieve the purpose of combining therapy of photodynamic therapy and chemotherapy.
    一种光敏剂及其衍生物的应用。该光敏剂具有一般式I的结构,其中X为S或Se,Y为有机或无机离子,R1和R2分别选自H、烷基、烷氧基、烷基酰胺基、烷基叠氮基等;R3选自H、烷基、烷氧基、氨基磺酰基、羟基、羧基等,L1为选自—(CH2)n1—或—(CH2CH2O)n2—的连接剂。这些衍生物是具有抗癌和化疗或肿瘤靶向功能的药物分子。该光敏剂具有优异的近红外特性和低暗毒性,用于光动力学肿瘤治疗领域。将苯并噻嗪或苯并硒噻嗪引入具有肿瘤靶向功能的衍生物中,可以提高光敏剂在肿瘤组织中的特异性摄取。此外,临床抗癌药物可以引入苯并噻嗪或苯并硒噻嗪的结构中,以实现光动力疗法和化疗的联合治疗目的。
  • IRIDIUM COMPLEX COMPOUND, COMPOSITION CONTAINING THE COMPOUND AND SOLVENT, ORGANIC ELECTROLUMINESCENT ELEMENT CONTAINING THE COMPOUND, DISPLAY DEVICE, AND ILLUMINATION DEVICE
    申请人:MITSUBISHI CHEMICAL CORPORATION
    公开号:US20200317706A1
    公开(公告)日:2020-10-08
    Provided is an iridium complex compound represented by formula (1) below. [Ir is an iridium atom. C 1 to C 6 are carbon atoms. N 1 and N 2 are nitrogen atoms. R 1 to R 4 are each a hydrogen atom or a substituent. a to d are maximum integer numbers of possible substituents on rings Cy 1 to Cy 4 , respectively. m and n are each 1 or 2, and m+n=3. The ring Cy 1 is represented by formula (2) or (2′) below. The ring Cy 3 is an aromatic or heteroaromatic ring including the carbon atoms C 4 and C 5 . The ring Cy 4 is a heteroaromatic ring including the carbon atom C 6 and the nitrogen atom N 2 .]
    提供的铱配合物化合物的化学式如下所示。 [Ir 代表铱原子。C1到C6代表碳原子。N1和N2代表氮原子。R1到R4分别代表氢原子或取代基。a到d分别代表环Cy1到Cy4上可能的取代基的最大整数个数。m和n分别为1或2,且m+n=3。环Cy1的化学式如下所示。环Cy3是包括碳原子C4和C5的芳香或杂芳环。环Cy4是包括碳原子C6和氮原子N2的杂芳环。]
  • Radical Route to 1,4-Benzothiazine Derivatives from 2-Aminobenzenethiols and Ketones under Transition-Metal-Free Conditions
    作者:Ya-mei Lin、Guo-ping Lu、Rong-kang Wang、Wen-bin Yi
    DOI:10.1021/acs.orglett.6b03324
    日期:2016.12.16
    Transition-metal-free radical access to 1,4-benzothiazine derivatives from o-aminobenzenethiols is disclosed. This procedure is available for various ketones including α,β-unsaturated, cyclic, linear, and fluoroalkyl ketones to generate a number of 1,4-benzothiazines, which exist in numerous bioactive and natural molecules, rendering this protocol attractive to both synthetic and medicinal chemistry
    公开了过渡金属自由基从邻氨基苯硫醇得到1,4-苯并噻嗪衍生物的方法。此程序可用于各种酮,包括α,β-不饱和,环状,线性和氟代烷基酮,生成大量存在于许多生物活性和天然分子中的1,4-苯并噻嗪,使该方案对合成和药用都具有吸引力化学。
  • Antimicrobial photoinactivation using chalcogen analogs of benzo(A)phenoxazinium dyes
    申请人:Hamblin R. Michael
    公开号:US20080015189A1
    公开(公告)日:2008-01-17
    Compositions and methods for the use of photoactivatable antimicrobial chalcogen analogs of benzophenoxazinium dyes in the treatment of infections are provided.
    提供了一种在治疗感染中使用光活化抗菌硒类类似物苯并噁唑啉染料的组合物和方法。
  • [EN] BIS(DIAZIRINE) DERIVATIVES AS PHOTO-CROSSSLINKER FOR TREATING CORNEAL ECTATIC DISORDERS<br/>[FR] DÉRIVÉS DE BIS(DIAZIRINE) UTILISÉS EN TANT QU'AGENT DE PHOTO-RÉTICULATION POUR LE TRAITEMENT DE TROUBLES ECTASIQUES DE LA CORNÉE
    申请人:AVEDRO INC
    公开号:WO2020154673A1
    公开(公告)日:2020-07-30
    This disclosure features bis(diazirine) derivatives of the formulae (I) (l-a) or (l-b) that generate cross-linking in the cornea in response to exposure to an electromagnetic irradiation (e.g. UV-light). The compounds are useful, e.g. for treating a subject (e.g. a human) having a disease, disorder or condition in which abnormal shaping of the cornea (e.g. thinning of the cornea, e.g. bilateral thinning of the cornea, e.g. bilateral thinning of the central, paracentral, or peripheral cornea, or steepening (e.g., bulging) of the cornea) contributes to the pathology and/or symptoms, and/or progression of the disease, disorder or condition. Examples of such diseases, disorders or conditions include: (i) corneal ectatic disorders; (ii) vision conditions; and (iii) diseases, disorders, or conditions that are sequela or comorbid with any of the foregoing or any disclosed herein. More particular examples of such diseases, disorders or conditions include keratoconus, keratoglobus, pellucid marginal degeneration, corneal ectasia (e.g. postoperative ectasia, e.g. post-LASIK ectasia), Terrien's marginal degeneration, myopia, hyperopia, astigmatism, irregular astigmatism and presbyopia. In some embodiments, the claimed methods can be performed in the absence of added or supplemental oxygen levels, which can be advantageous in some applications. Preferred exemplary compounds are e.g. bis(diazirine) amino acid derivatives, such as e.g. example 1:
    这份披露涉及到式(I) (l-a)或(l-b)的双(重氮基)衍生物,当暴露于电磁辐射(例如紫外光)时,在角膜中产生交联作用。这些化合物可用于治疗患有疾病、疾病或病况的受试者(例如人类),其中角膜的异常形态(例如角膜变薄,例如角膜双侧变薄,例如角膜中央、副中央或周边变薄,或角膜变陡(例如突出))导致病理和/或症状的发生,以及/或疾病、疾病或病况的进展。此类疾病、疾病或病况的示例包括:(i) 角膜扩张性疾病;(ii) 视力状况;以及(iii) 与前述任何疾病、疾病或病况或本文所披露的任何内容相关的后遗症或共病。此类疾病、疾病或病况的更具体示例包括角膜锥状变性、角膜球状变性、边缘淡化变性、角膜扩张(例如术后扩张,例如术后LASIK扩张)、Terrien边缘变性、近视、远视、散光、不规则散光和老视。在某些实施例中,声称的方法可以在没有额外或补充氧气水平的情况下进行,这在某些应用中可能是有利的。优选的示例化合物包括双(重氮基)氨基酸衍生物,例如示例1:
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