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1-苯氧基-2-丙氧基-乙烷 | 100057-20-3

中文名称
1-苯氧基-2-丙氧基-乙烷
中文别名
——
英文名称
1-phenoxy-2-propoxy-ethane
英文别名
1-Phenoxy-2-propoxy-aethan;(2-propoxyethoxy)benzene;2-Phenoxyethanol, n-propyl ether;2-propoxyethoxybenzene
1-苯氧基-2-丙氧基-乙烷化学式
CAS
100057-20-3
化学式
C11H16O2
mdl
——
分子量
180.247
InChiKey
AJPRRDSJGHIUKH-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

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    13
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • NOVEL SEMI-SYNTHETIC GLYCOPEPTIDES AS ANTIBACTERIAL AGENTS
    申请人:Chu Daniel
    公开号:US20100105607A1
    公开(公告)日:2010-04-29
    Semi-synthetic glycopeptides having antibacterial activity are described, in particular, the semi-synthetic glycopeptides described herein are made by chemical modification of the a glycopeptide (Compound A, Compound B, Compound H or Compound C) or the monosaccharide made by hydrolyzing the disaccharide moiety of the amino acid-4 of the parent glycopeptide in acidic medium to give the amino acid-4 monosaccharide; conversion of the monosaccharide to the amino-sugar derivative; acylation of the amino substituent on the amino acid-4 amino-substituted sugar moiety on these scaffolds with certain acyl groups; conversion of the amide group in amino acid-3 on these scaffolds to various acylamide, acylsulfonamide, acylsulfonylurea derivatives; aminomethylation with substituent containing sulfonamide or acylsulfonamide group on amino acid-7 through Mannich reaction; and conversion of the acid moiety on the macrocyclic ring of these scaffolds to certain substituted amides. Also provided are methods for the synthesis of the compounds, pharmaceutical compositions containing the compounds, and methods of use of the compounds for the treatment and/or prophylaxis of diseases, especially bacterial infections.
    所描述的具有抗菌活性的半合成糖肽,特别是这里描述的半合成糖肽是通过对一种糖肽(化合物A、化合物B、化合物H或化合物C)进行化学修饰制备的,或者通过在酸性介质中氨基酸-4的二糖基团以得到氨基酸-4单糖基团;将单糖转化为基糖衍生物;用特定酰基对这些支架上氨基酸-4基取代糖基团上的基取代基进行酰化;将这些支架上氨基酸-3中的酰胺基团转化为各种酰胺、酰磺酰胺、酰磺酰生物;通过曼尼希反应在氨基酸-7上含有磺胺基或酰磺酰胺基团的取代基上进行甲基化;以及将这些支架上大环环上的酸基团转化为特定取代酰胺。还提供了合成这些化合物的方法,含有这些化合物的药物组合物,以及这些化合物用于治疗和/或预防疾病,特别是细菌感染的方法。
  • METHOD FOR PRODUCING ALPHA-HALOGENOACETOPHENON COMPOUND, AND ALPHA-BROMOACETOPHENON COMPOUND
    申请人:FUJIFILM Corporation
    公开号:US20160200654A1
    公开(公告)日:2016-07-14
    A method for producing an α-halogenoacetophenon compound includes reacting a specific α-halogenocarboxylic halide compound and a specific phenyl compound in the presence of a Lewis acid in a solvent, in which the α-halogenoacetophenon compound and the phenyl compound are reacted with each other in a molar ratio of the Lewis acid to the phenyl compound represented below. 2≦Lewis acid/phenyl compound≦6
    生产α-卤代乙酰苯酮化合物的方法包括在溶剂中,在Lewis酸的存在下,反应特定的α-卤代羧酸卤化物化合物和特定的苯化合物,其中α-卤代乙酰苯酮化合物和苯化合物按照以下所示的Lewis酸与苯化合物的摩尔比进行反应。2≦Lewis酸/苯化合物≦6
  • MODULATORS OF BTK PROTEOLYSIS AND METHODS OF USE
    申请人:Yale University
    公开号:US20190276459A1
    公开(公告)日:2019-09-12
    The present disclosure relates to bifunctional compounds, which find utility as modulators of Burton's Tyrosine Kinase (BTK). In particular, the present disclosure is directed to bifunctional compounds. One end of a bifunctional compound includes a Von Hippel-Lindau, Cereblon, Inhibitors of Apotosis Proteins, or Mouse Double-Minute Homolog 2 ligand that binds to the respective E3 ubiquitin ligase. The other end of a bifunctional compound includes a moiety that binds a target protein, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. Diseases or disorders that result from aggregation, accumulation, and/or overactivation of the target protein can be treated or prevented with compounds and compositions of the present disclosure.
    本公开涉及双功能化合物,其作为Burton的酪氨酸激酶(BTK)的调节剂而有用。特别是,本公开是针对双功能化合物的。双功能化合物的一端包括Von Hippel-Lindau、Cereblon、Inhibitors of Apotosis Proteins或Mouse Double-Minute Homolog 2配体,该配体结合到相应的E3泛素连接酶。双功能化合物的另一端包括结合到目标蛋白质的部分,使目标蛋白质靠近泛素连接酶,以促进目标蛋白质的降解(和抑制)。本公开的化合物和组合物可用于治疗或预防由目标蛋白质的聚集、积累和/或过度活化引起的疾病或障碍。
  • COMPOUND, RESIN, COMPOSITION, RESIST PATTERN FORMATION METHOD, CIRCUIT PATTERN FORMATION METHOD, AND METHOD FOR PURIFYING RESIN
    申请人:Mitsubishi Gas Chemical Company, Inc.
    公开号:US20220144738A1
    公开(公告)日:2022-05-12
    The present invention has an object to provide a new compound that is useful as a film forming material for lithography or an optical component forming material, a resin containing a constituent unit derived from said compound, a composition, a resist pattern formation method, a circuit pattern formation method, and a purification method. A compound represented by formula (1), a resin containing a constituent unit derived from said compound, a composition containing one or more selected from the group consisting of said compound and said resin, a resist pattern formation method using said composition, a circuit pattern formation method, and a purification method thereof.
    本发明的目的是提供一种新的化合物,该化合物可用作光刻膜形成材料或光学元件形成材料,以及含有源自该化合物的组成单元的树脂、组合物、利用该组合物进行的抗蚀图案形成方法、电路图案形成方法和纯化方法。该化合物由式(1)表示,含有源自该化合物的组成单元的树脂,含有来自该化合物和/或该树脂的一种或多种的组合物,利用该组合物进行的抗蚀图案形成方法、电路图案形成方法和纯化方法。
  • Liquid crystal orienting agent
    申请人:JAPAN SYNTHETIC RUBBER CO., LTD.
    公开号:EP0735403A1
    公开(公告)日:1996-10-02
    A liquid crystal aligning agent contains (1) at least one polymer selected from the group consisting of a polyamic acid obtainable by a reaction between a tetracarboxylic acid dianhydride and a diamine compound and an imidized polymer obtainable by cyclization with dehydration of the polyamic acid; (2) at least one first solvent selected from the group consisting of N-alkyl-2-pyrrolidones, lactones, and 1,3-dialkyl-2-imidazolidinones; (3) at least one second solvent selected from the group consisting of: (a) a first compound represented by general formula (I) wherein R1 is an alkylene group having 2 or 3 carbon atoms; R2 is an alkyl group having 1 to 4 carbon atoms an acetyl group or a propionyl group; R3 is an alkyl group having 1 to 3 carbon atoms, an alkoxyl group having 1 to 3 carbon atoms, or a halogen atom; a is 1 or 2; and b is 0 or integers of from 1 to 5; and (b) a second compound represented by general formula (II) wherein R4 is an alkyl group having 1 to 4 carbon atoms; R5 is an alkylene group having 2 or 3 carbon atoms; R6 is an alkyl group having 1 to 3 carbon atoms; and c is 1 or 2.
    液晶对准剂包含 (1) 至少一种聚合物,选自由四羧酸二酐和二胺化合物反应生成的聚基 酸和聚氨基酸环化生成的亚胺化聚合物组成的组; (2) 至少一种第一溶剂,选自由 N-烷基-2-吡咯烷酮、内酯和 1,3-二烷基-2-咪唑烷酮组成的组; (3) 至少一种第二溶剂,选自由下列物质组成的组 (a) 通式 (I) 所代表的第一种化合物 其中 R1 是具有 2 或 3 个碳原子的亚烷基;R2 是具有 1 至 4 个碳原子的烷基、乙酰基或丙酰基;R3 是具有 1 至 3 个碳原子的烷基、具有 1 至 3 个碳原子的烷氧基或卤原子;a 是 1 或 2;b 是 0 或 1 至 5 的整数;以及 (b) 通式(II)代表的第二种化合物 其中 R4 是具有 1 至 4 个碳原子的烷基;R5 是具有 2 或 3 个碳原子的亚烷基;R6 是具有 1 至 3 个碳原子的烷基;以及 c 是 1 或 2。
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(R)-3-(叔丁基)-4-(2,6-二异丙氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (2S,3R)-3-(叔丁基)-2-(二叔丁基膦基)-4-甲氧基-2,3-二氢苯并[d][1,3]氧杂磷杂戊环 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-二甲氧基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2R,2''R,3R,3''R)-3,3''-二叔丁基-4,4''-二甲氧基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2-氟-3-异丙氧基苯基)三氟硼酸钾 (+)-6,6'-{[(1R,3R)-1,3-二甲基-1,3基]双(氧)}双[4,8-双(叔丁基)-2,10-二甲氧基-丙二醇 麦角甾烷-6-酮,2,3,22,23-四羟基-,(2a,3a,5a,22S,23S)- 鲁前列醇 顺式6-(对甲氧基苯基)-5-己烯酸 顺式-铂戊脒碘化物 顺式-四氢-2-苯氧基-N,N,N-三甲基-2H-吡喃-3-铵碘化物 顺式-4-甲氧基苯基1-丙烯基醚 顺式-2,4,5-三甲氧基-1-丙烯基苯 顺式-1,3-二甲基-4-苯基-2-氮杂环丁酮 非那西丁杂质7 非那西丁杂质3 非那西丁杂质22 非那西丁杂质18 非那卡因 非布司他杂质37 非布司他杂质30 非布丙醇 雷诺嗪 阿达洛尔 阿达洛尔 阿莫噁酮 阿莫兰特 阿维西利 阿索卡诺 阿米维林 阿立酮 阿曲汀中间体3 阿普洛尔 阿普斯特杂质67 阿普斯特中间体 阿普斯特中间体 阿托西汀EP杂质A 阿托莫西汀杂质24 阿托莫西汀杂质10 阿托莫西汀EP杂质C 阿尼扎芬 阿利克仑中间体3 间苯胺氢氟乙酰氯 间苯二酚二缩水甘油醚 间苯二酚二异丙醇醚 间苯二酚二(2-羟乙基)醚 间苄氧基苯乙醇 间甲苯氧基乙酸肼 间甲苯氧基乙腈 间甲苯异氰酸酯