N-(2-甲基丙基)-(9ci)-2-氨基苯并噻唑 | 24622-32-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻唑类
• 中文名称: N-(2-甲基丙基)-(9ci)-2-氨基苯并噻唑
• 英文名称: N-isobutylbenzo[d]thiazol-2-amine
• 英文别名: 2-iso-Butylamino-benzthiazol；2-Benzothiazolamine, N-(2-methylpropyl)-；N-(2-methylpropyl)-1,3-benzothiazol-2-amine
• CAS: 24622-32-0
• 化学式: C₁₁H₁₄N₂S
• mdl: MFCD03152764
• 分子量: 206.312
• InChiKey: SMGKWHWIOTWYOI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.363
• 拓扑面积：
  53.2
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 海关编码：
  2934999090

反应信息

• 作为反应物：
  描述：

  N-(2-甲基丙基)-(9ci)-2-氨基苯并噻唑 在 氯仿 、 溴 作用下， 生成 (6-bromo-benzothiazol-2-yl)-isobutyl-amine
  参考文献：
  名称：

  Farooq; Hunter; Jaffery, Journal of the Indian Chemical Society, 1933, vol. 10, p. 189

  摘要：

  DOI：
• 作为产物：
  描述：

  N-(2-甲基丙基)-N'-苯基硫脲 在 lead(II) dihydrogen orthophosphate 、 H2 、 buffer solution 作用下， 以 甲醇 为溶剂， 反应 1.5h， 生成 N-(2-甲基丙基)-(9ci)-2-氨基苯并噻唑
  参考文献：
  名称：

  El-Meligy,M.S.A.; Mohamed,S.A., Journal fur praktische Chemie (Leipzig 1954), 1974, vol. 316, p. 154 - 158

  摘要：

  DOI：

文献信息

• METHOD FOR PRODUCING 2-HYDRAZINOBENZOTHIAZOLE DERIVATIVE
  申请人：DIC Corporation

  公开号：US20200165215A1

  公开（公告）日：2020-05-28

  The present invention provides a novel method for producing a 2-hydrazinobenzothiazole derivative. The present invention also provides a method for producing a compound by using the 2-hydrazinobenzothiazole derivative obtained by the production method, and a composition that contains the compound. The present invention also provides a polymerizable composition that is useful in producing film-shaped polymers and contains the compound obtained by the production method. The invention of the present application provides a method for producing a compound represented by general formula (I-C), the method including a step of reacting a compound represented by general formula (I-B) with a compound represented by general formula (I-A) in the presence of at least one compound selected from the group consisting of metal amides, metal hydrides, metal alkoxides, and organic alkali metals. A compound derived from the compound produced by the production method, and a composition that contains the compound are also provided.

  本发明提供一种生产2-联苯并噻唑酮衍生物的新方法。本发明还提供一种通过使用通过生产方法获得的2-联苯并噻唑酮衍生物生产化合物的方法，以及含有该化合物的组合物。本发明还提供一种可用于生产膜状聚合物的可聚合组合物，其中包含通过生产方法获得的化合物。本申请的发明提供了一种生产通式(I-C)所代表的化合物的方法，该方法包括在至少选择自金属胺、金属氢化物、金属烷氧化物和有机碱金属组成的群体中，通过将通式(I-B)所代表的化合物与通式(I-A)所代表的化合物在存在下反应的步骤。还提供了通过生产方法产生的化合物衍生物以及含有该化合物的组合物。
• CD4-MIMETIC INHIBITORS OF HIV-1 ENTRY AND METHODS OF USE THEREOF
  申请人：Dana-Farber Cancer Institute, Inc.

  公开号：US20140350113A1

  公开（公告）日：2014-11-27

  Described herein are small-molecule mimics of CD4, which both enter the Phe43 cavity and target Asp368 of gp120, the HIV-1 envelope protein. Also described herein are methods of using these compounds to inhibit the transmission or progression of HIV infection. These compounds exhibit antiviral potency greater than that of a known antiviral, NBD-556, with 100% breadth against clade B and C viruses. Importantly, the compounds do not activate HIV infection of CD4-negative, CCR5-positive cells, in contrast to NBD-556.

  本文描述了CD4的小分子模拟物，它们进入Phe43腔并靶向HIV-1包膜蛋白gp120的Asp368。本文还描述了使用这些化合物抑制HIV感染的传播或进展的方法。这些化合物表现出比已知抗病毒药物NBD-556更强的抗病毒效力，对B和C类病毒具有100％的广度。重要的是，与NBD-556相比，这些化合物不会激活CD4阴性，CCR5阳性细胞的HIV感染。
• Method for producing polymerizable compound
  申请人：DIC Corporation

  公开号：US10927087B2

  公开（公告）日：2021-02-23

  The polymerizable compound has a hydrazone moiety. The present invention also provides a polymerizable composition in which discoloration and reduction of aligning property do not easily occur. Furthermore, the present invention provides a polymer obtained by polymerizing a polymerizable composition containing a compound obtained by the production method and an optically anisotropic body using the polymer. The present invention provides a method for producing a polymerizable compound including a step of reacting a compound represented by General Formula (I-B-a) with a compound represented by General Formula (I-B-b) to obtain a compound represented by General Formula (I-C), and provides a composition which contains a compound obtained by this production method.

  可聚合化合物具有腙分子。本发明还提供了一种不易发生变色和对准性能降低的可聚合组合物。此外，本发明还提供了一种通过聚合含有通过上述生产方法获得的化合物的可聚合组合物和使用该聚合物的光学各向异性体而获得的聚合物。本发明提供了一种生产可聚合化合物的方法，包括通式(I-B-a)代表的化合物与通式(I-B-b)代表的化合物反应得到通式(I-C)代表的化合物的步骤，并提供了一种含有通过该生产方法得到的化合物的组合物。
• Inhibiting germination of clostridium perfringens spores to reduce necrotic enteritis
  申请人：The Board of Regents of the Nevada System of Higher Education on Behalf of the University of Nevada

  公开号：US10945996B2

  公开（公告）日：2021-03-16

  Provided herein are materials and methods useful for reducing, preventing, and/or inhibiting germination of C. perfringens spores, including methods for inhibiting C. perfringens germination to reduce necrotizing enteritis (NE, also referred to as necrotic enteritis) in animals. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

  本文提供了用于减少、预防和/或抑制C. perfringens孢子萌发的材料和方法，包括抑制C. perfringens萌发以减少动物坏死性肠炎（NE，也称为坏死性肠炎）的方法。本摘要旨在作为特定技术领域的扫描工具，供检索之用，并非对本发明的限制。
• Laccase-Catalysed Homocoupling of Primary Aromatic Amines towards the Biosynthesis of Dyes
  作者：Ana Catarina Sousa、Lígia O. Martins、M. Paula Robalo

  DOI：10.1002/adsc.201300501

  日期：2013.10.11

  AbstractColoured disubstituted benzoquinonimine trimeric structures are obtained as main reaction products of the oxidation of p‐electron donor primary aromatic amines using two different laccases, CotA‐laccase from Baccilus subtilus and TvL from Trametes versicolor. These orange‐red to purple products, presenting high molar extinction coefficients, presumably result from oxidative homocoupling reactions, through the formation of NC bonds at positions 2 and 5, of the laccase oxidised intermediate as showed in the proposed oxidative pathway. The product of 1,4‐phenylenediamine is shown to be the trimer known as Bandrowski’s base which has an established role in hair and fur dyeing. Our results also show that the occurrence and/or rates of oxidation of aromatic amines are strongly dependent on the presence of p‐electron releasing substituents in the aromatic ring and are independent on the properties of the enzyme used. Overall our data contribute for (i) understanding key features of laccase reactivity with p‐substituted aromatic amines and (ii) establishing enzymatic processes that lead to the synthesis of coloured bio‐products under mild conditions with potential impact in the cosmetic and dye industries.magnified image