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3-Phenacylthiazolium

中文名称
——
中文别名
——
英文名称
3-Phenacylthiazolium
英文别名
1-phenyl-2-(1,3-thiazol-3-ium-3-yl)ethanone
3-Phenacylthiazolium化学式
CAS
——
化学式
C11H10NOS+
mdl
——
分子量
204.27
InChiKey
IBDBVEYUXOTRAO-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:
    14
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    49.2
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • Crosslink Breakers for Preservation of Biological Substances
    申请人:Spiegel David
    公开号:US20150099260A1
    公开(公告)日:2015-04-09
    A preservative for body fluids, proteins, cells and tissues comprising an effective amount of an AGE crosslink breaker for preventing formation of advanced glycation end products. The AGE crosslink breaker comprises a compound of Structure (1): wherein V, W, X, Y and Z are any atom suitable for a heterocyclic carbene or carbene precursor framework, including B, C, O, N, S, Se, P, and As in any chemically-feasible oxidation state; wherein Q, R, M, T and U are any atom or substituent, including but not limited to, H, CL n , NL n , PL n , OL n , SL n , SeL n , L n Cl, L n Br, L n I, wherein L is any atom, substituent or group, and n is any integer such that Q, R, M, T, and U can access all chemically-feasible oxidation states; and wherein G comprises any charged counter ion including, but not limited to those derived from C, O, N, B, Al, S, Se, Cl, Br, I in any chemically-feasible oxidation state.
    一种用于体液、蛋白质、细胞和组织的防腐剂,包括一种有效量的AGE交联断裂剂,用于预防高级糖基化终产物的形成。AGE交联断裂剂包括结构(1)中的化合物: 其中V、W、X、Y和Z是适用于杂环卡宾或卡宾前体框架的任何原子,包括B、C、O、N、S、Se、P和As在任何化学上可行的氧化态; 其中Q、R、M、T和U是任何原子或取代基,包括但不限于H、CLn、NLn、PLn、OLn、SLn、SeLn、LnCl、LnBr、LnI,其中L是任何原子、取代基或基团,n是任何整数,使得Q、R、M、T和U可以访问所有化学上可行的氧化态;以及 其中G包括任何带电的对离子,包括但不限于那些来源于C、O、N、B、Al、S、Se、Cl、Br、I在任何化学上可行的氧化态。
  • [EN] FUSED QUINOLINE DERIVATIVE AND USE THEREOF<br/>[FR] DÉRIVÉ DE QUINOLINE FUSIONNÉE ET UTILISATION DE CELUI-CI
    申请人:TAKEDA PHARMACEUTICAL
    公开号:WO2005105802A1
    公开(公告)日:2005-11-10
    The present invention aims at provision of a quinoline derivative having a neurokinin 2 (NK2) receptor antagonistic action and relates to a compound represented by the formula (I) wherein Rl is a hydrogen atom and the like; R2 is a hydrogen atom, a hydrocarbon group optionally having substituent(s) and the like; R3 is unsubstituted (i.e., absence), a hydrogen atom and the like; R4 and R5 are the same or different and each is a hydrogen atom, a hydrocarbon group optionally having substituent(s), and the like; R6 is (cyclic group optionally having substituent(s)) -carbonyl, and the like; R7, R8, R9 and R10 are the same or different and each is a hydrogen atom, halogen and the like; or R7 and R8, R8 and R9, and R9 and R10 may form a ring together with the adjacent carbon atoms; n is an integer of 1 to 5; --- represents unsubstituted (i.e., absence) or a single bond; and --- represents a single bond or a double bond, or a salt thereof, and the like.
    本发明旨在提供一种具有神经激肽2(NK2)受体拮抗作用的喹啉衍生物,并涉及一种由式(I)表示的化合物,其中R1是氢原子等;R2是氢原子,可选地具有取代基的碳氢基团等;R3是未取代的(即缺失),氢原子等;R4和R5相同或不同,每个是氢原子,可选地具有取代基的碳氢基团等;R6是(环状基团,可选地具有取代基)-羰基等;R7、R8、R9和R10相同或不同,每个是氢原子,卤素等;或R7和R8、R8和R9、以及R9和R10可以与相邻的碳原子一起形成环;n是1到5的整数;---表示未取代的(即缺失)或单键;---表示单键或双键,或其盐等。
  • PREVENTION OF BODY ODOUR
    申请人:Huchel Ursula
    公开号:US20120164097A1
    公开(公告)日:2012-06-28
    Bad odors on textile materials are often caused by body odor. The invention relates to a textile material treatment method for inhibiting body odor on textile materials, by which means the treated textiles, after having been worn, even after sweat-inducing sports activities, have a significantly reduced bad odor or even no odor. The invention also relates to a perfume composition and to a textile material treatment agent, respectively comprising urea derivatives and/or phenacylthiazolium salts, that counteract the formation of body odor.
    纺织材料上的不良气味通常是由体臭引起的。本发明涉及一种抑制纺织材料上体臭的纺织材料处理方法,通过该方法处理的纺织品,即使在进行导致出汗的运动活动后穿着,也能显著减少不良气味甚至没有气味。本发明还涉及一种香水组合物以及一种纺织材料处理剂,分别包含尿素衍生物和/或苯乙基亚砜盐,它们能对抗体臭的形成。
  • Method and composition for rejuvenating hair, nails, tissues, cells and organs by ex-vivo or immersive treatment
    申请人:——
    公开号:US20020182165A1
    公开(公告)日:2002-12-05
    A method and composition for the treatment of hair, nail, ex-vivo organ, ex-vivo cell or ex-vivo tissue to improve the biomechanical and diffusional characteristics comprising an effective amount of a compound selected from the group consisting of compounds of the formula 1
    一种用于改善生物力学和扩散特性的头发、指甲、离体器官、离体细胞或离体组织的治疗方法和组合物,包括有效量的来自化合物公式1所述化合物组合的化合物。
  • CYCLIC SULFONIUM SALT, METHOD FOR PRODUCTION OF CYCLIC SULFONIUM SALT, AND GLYCOSIDASE INHIBITOR
    申请人:Muraoka Osamu
    公开号:US20100063302A1
    公开(公告)日:2010-03-11
    Disclosed are: kotalanol which has an inhibitory activity on a glucosidase; a method for producing kotalanol or a cyclic sulfonium salt which is an analogue to kotalanol by an organic synthesis technique; a cyclic sulfonium salt produced by the method; a glucosidase inhibitor comprising the compound; an anti-diabetic agent or an anti-diabetic food comprising the glucosidase inhibitor. A sulfonium compound including kotalanol can be produced by coupling a thio-sugar synthesized from D-xylose (e.g., a compound having a cyclic structure composed of 4 carbon atoms and one sulfur atom, such as 1,4-dideoxy-1,4-epithio-D-arabinitol) with a heptitol cyclic sulfate ester having a protected hydroxyl group and synthesized from a pentose (D-xylose, D-ribose, D-arabinose, D-lyxose, L-xylose, L-ribose, L-arabinose or L-lyxose) to produce a cyclic sulfonium salt having a protected hydroxyl group, and then deprotecting the hydroxyl group.
    本发明涉及一种对葡萄糖苷酶具有抑制活性的kotalanol;一种通过有机合成技术制备kotalanol或类似kotalanol的环状亚磺酸盐的方法;一种通过该方法制备的环状亚磺酸盐;一种包含该化合物的葡萄糖苷酶抑制剂;一种包含该葡萄糖苷酶抑制剂的抗糖尿病剂或抗糖尿病食品。可以通过将从D-木糖合成的硫代糖(例如,由4个碳原子和1个硫原子组成的环状结构化合物,如1,4-二去氧-1,4-环硫-D-阿拉伯糖醇)与从戊糖(D-木糖,D-核糖,D-阿拉伯糖,D-吕氏木糖,L-木糖,L-核糖,L-阿拉伯糖或L-吕氏木糖)合成的带有保护羟基的庚糖环硫酸酯偶联,以制备具有保护羟基的环状亚磺酸盐,然后去保护羟基来制备包含kotalanol的亚磺酸化合物。
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