4-甲氧基-2-甲基硫代苯酚 | 698-81-7

• 物质功能分类: 化学试剂 - 有机试剂 - 硫醇/硫酚
• 分子结构分类: 有机化合物 - 苯类化合物 - 苯硫酚类
• 中文名称: 4-甲氧基-2-甲基硫代苯酚
• 中文别名: 4-甲氧基-2-甲基苯硫酚
• 英文名称: 5-methoxy-2-mercapto-toluene
• 英文别名: Methyl-(4-mercapto-3-methyl-phenyl)-aether；4-Methoxy-2-methyl-phenylmercaptan；5-Methoxy-2-mercapto-toluol；4-methoxy-2-methylbenzenethiol；2-Methyl-4-methoxyphenylmercaptan；4-Methoxy-2-methyl-thiophenol；4-Methoxy-2-methylthiophenol
• CAS: 698-81-7
• 化学式: C₈H₁₀OS
• 分子量: 154.233
• InChiKey: WXKKTBSADLTBPS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  10.2
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 海关编码：
  2930909090

反应信息

• 作为反应物：
  描述：

  4-甲氧基-2-甲基硫代苯酚 在 sodium hydroxide 、 氢溴酸 、 溶剂黄146 作用下， 生成 3-甲基-4-甲硫基苯酚
  参考文献：
  名称：

  The Preparation and Germicidal Properties of 2-Methyl-4-hydroxyphenyl Alkyl Sulfides

  摘要：

  DOI：

  10.1021/ja01326a079
• 作为产物：
  描述：

  2-bromo-4-methoxy-benzenethiocyanate 生成 4-甲氧基-2-甲基硫代苯酚
  参考文献：
  名称：

  SCHNEIDER, JOSEF A.

  摘要：

  DOI：

文献信息

• [EN] NUCLEOSIDE PHOSPHONATE DERIVATIVES USEFUL IN THE TREATMENT OF HIV INFECTIONS<br/>[FR] DERIVES DE NUCLEOSIDE PHOSPHONATE UTILES DANS LE TRAITEMENT D'INFECTIONS VIH
  申请人：ANADYS PHARMACEUTICALS INC

  公开号：WO2005079812A1

  公开（公告）日：2005-09-01

  The present invention relates to a method of treating HIV infections by administering a nucleoside phosphonate derivative represented by formula (I).

  本发明涉及通过给予由式(I)表示的核苷酸膦酸衍生物来治疗HIV感染的方法。
• [EN] (+)-TRANS-ISOMERS OF (1-PHOSPHONOMETHOXY-2-ALKYLCYCLOPROPYL) METHYL NUCLEOSIDE DERIVATIVES, PROCESS FOR THE PREPARATION OF STEREOISOMERS THEREOF, AND USE OF ANTIVIRAL AGENTS THEREOF<br/>[FR] TRANS-ISOMERES (+) DE DERIVES DE NUCLEOSIDE ( 1-PHOSPHONOMETHOXY-2-ALKYLCYCLOPROPYL)METHYLE, PROCESSUS DE PREPARATION DE STEREO-ISOMERES DE CEUX-CI ET UTILISATION D'AGENTS ANTIVIRAUX A BASE CEUX-CI
  申请人：LG LIFE SCIENCES LTD

  公开号：WO2004029064A1

  公开（公告）日：2004-04-08

  The present invention relates to (+)-trans-isomers of (1-phosphonomethoxy-2- alkylcyclopropyl)methyl nucleoside derivatives of the formula (1) which are useful as an antiviral agent (particularly, against hepatitis B virus), pharmaceutically acceptable saltss, hydrates, or solvates thereof, and processes for the preparation of stereoisomers of the compounds of the formula (1), and a composition for the treatment of viral diseases (particularly, against hepatitis B virus) comprising (+)-trans-isomer of the compound of the formula (1), pharmaceutically acceptable salt, hydrate, or solvate thereof as an active substance.

  本发明涉及公式（1）的（+）-反式异构体（1-磷酸甲氧基-2-烷基环丙基）甲基核苷衍生物，该衍生物可用作抗病毒剂（特别是对乙型肝炎病毒），其药用盐、水合物或溶剂化合物，以及用于制备公式（1）化合物的立体异构体的方法，以及一种用于治疗病毒性疾病（特别是对乙型肝炎病毒）的组合物，包括公式（1）化合物的（+）-反式异构体，其药用盐、水合物或溶剂化合物作为活性物质。
• Hexahydro-(1)-benzo-(pyrano and thiopyrano) (4,3-C)pyridines, useful as
  申请人：Ciba-Geigy Corporation

  公开号：US04666916A1

  公开（公告）日：1987-05-19

  Disclosed are the compounds of the formula ##STR1## wherein X represents oxygen (O) or sulfur (S); ring A is unsubstituted or substituted by one substituent or by two or three identical or different substituents selected from hydroxy, etherified hydroxy, acyloxy, halogen, lower alkyl and trifluoromethyl; or ring A is substituted on adjacent carbon atoms by one lower alkylenedioxy; R represents hydrogen, lower alkyl, aryl-lower alkyl, lower alkenyl, lower alkynyl, aroyl-lower alkyl or aryl-lower alkyl; R.sub.1 represents hydrogen, lower alkyl, lower alkylthio-lower alkyl, aryl-lower alkylthio-lower alkyl, (amino, mono- or di-lower alkylamino)-lower alkyl, acylamino-lower alkyl, (hydroxy, acyloxy or etherified hydroxy)-lower alkyl, or cyano-lower alkyl; R.sub.2 -R.sub.7 represent hydrogen or lower alkyl; and pharmaceutically acceptable salts thereof; which are useful as serotonin-2 receptor antagonists in mammals.

  本文揭示了具有以下结构的化合物：其中X代表氧（O）或硫（S）；环A未取代或被一个取代基或两个或三个相同或不同的取代基取代，所选取代基包括羟基、醚化羟基、酰氧基、卤素、低碳基和三氟甲基；或者环A在相邻的碳原子上被一个低碳基二氧取代；R代表氢、低碳基、芳基-低碳基、低烯基、低炔基、芳酰基-低碳基或芳基-低碳基；R.sub.1代表氢、低碳基、低碳硫基-低碳基、芳基-低碳硫基-低碳基、（氨基、单或双低碳氨基）-低碳基、酰胺基-低碳基、（羟基、酰氧基或醚化羟基）-低碳基或氰基-低碳基；R.sub.2 - R.sub.7代表氢或低碳基；以及其药学上可接受的盐；这些化合物在哺乳动物中作为5-羟色胺-2受体拮抗剂是有用的。
• NAPHTHALOCYANINE COMPOUND, METHOD FOR PRODUCING SAME, AND USE THEREOF
  申请人：YAMAMOTO CHEMICALS, INC.

  公开号：US20210107924A1

  公开（公告）日：2021-04-15

  Provided are a novel naphthalocyanine compound, which has strong absorption in a near-infrared range, extremely weak absorption in a visible range, and high resistance such as light resistance and heat resistance, and exhibits excellent solubility in an organic solvent or a resin, a heat ray shielding material, and uses of the naphthalocyanine compound such as a heat ray shielding material and the like. The naphthalocyanine compound is represented by General Formula (1). wherein, in Formula (1), M represents two hydrogen atoms, a divalent metal, or a derivative of a trivalent or tetravalent metal, R 1 to R 3 each independently represent a hydrogen atom, a halogen atom, or a linear, branched, or cyclic alkyl group, A represents Formula (2), and B represents Formula (3), wherein, in Formula (2), R 4 to R 8 each independently represent a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an alkylthio group, an aryloxy group, or an arylthio group, and wherein, in Formula (3), X represents an oxygen atom, a sulfur atom, and or an imino group, R 9 to R 13 each independently represent a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an ester group, an amide group, or a sulfonamide group.

  提供了一种新型萘酞菁化合物，它在近红外范围内具有强烈的吸收能力，在可见光范围内具有极弱的吸收能力，并具有高耐光性和耐热性，并在有机溶剂或树脂中表现出优异的溶解性能，可用作热辐射屏蔽材料，以及该萘酞菁化合物的用途，例如热辐射屏蔽材料等。该萘酞菁化合物由通式（1）表示。在式（1）中，M代表两个氢原子、二价金属或三价或四价金属的衍生物，R1至R3各自独立地表示氢原子、卤素原子或线性、支链或环烷基，A代表式（2），B代表式（3），在式（2）中，R4至R8各自独立地表示氢原子、卤素原子、烷基、烷氧基、烷硫基、芳氧基或芳硫基，在式（3）中，X表示氧原子、硫原子或亚胺基，R9至R13各自独立地表示氢原子、卤素原子、烷基、烷氧基、酯基、酰胺基或磺酰胺基。
• [EN] NOVEL ACYCLIC NUCLEOSIDE PHOSPHONATE DERIVATIVES, SALTS THEREOF AND PROCESS FOR THE PREPARATION OF THE SAME<br/>[FR] NOUVEAUX DERIVES DE PHOSPHONATE NUCLEOSIDIQUE ACYCLIQUE, SELS DE CES DERNIERS ET PROCEDE DE PREPARATION DE CES DERNIERS
  申请人：LG CHEM INVESTMENT LTD

  公开号：WO2002057288A1

  公开（公告）日：2002-07-25

  The present invention relates to an acyclic nucleoside phosphonate derivative, which is useful as an antiviral agent (particularly, against hepatitis B virus), pharmaceutically acceptable salts, stereoisomers, and a process for the preparation thereof.

  本发明涉及一种无环核苷酸膦酸酯衍生物，其作为抗病毒剂（特别是对乙型肝炎病毒）有用，药学上可接受的盐，立体异构体以及其制备方法。