摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-<5-anilino-3-chloro-2,4-(propane-1',3'-diyl)-2,4-pentadien-1-ylidene>anilinium chloride | 195382-10-6

中文名称
——
中文别名
——
英文名称
N-<5-anilino-3-chloro-2,4-(propane-1',3'-diyl)-2,4-pentadien-1-ylidene>anilinium chloride
英文别名
(E)-[(3E)-3-(anilinomethylidene)-2-chlorocyclohexen-1-yl]methylidene-phenylazanium;chloride
N-<5-anilino-3-chloro-2,4-(propane-1',3'-diyl)-2,4-pentadien-1-ylidene>anilinium chloride化学式
CAS
195382-10-6
化学式
C20H19ClN2*ClH
mdl
——
分子量
359.298
InChiKey
VFKQWKQWRNVXTA-LPYKZFQHSA-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):
    6.48
  • 重原子数:
    24.0
  • 可旋转键数:
    4.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    24.39
  • 氢给体数:
    1.0
  • 氢受体数:
    2.0

反应信息

点击查看最新优质反应信息

文献信息

  • NIR TO SWIR FLUORESCENT COMPOUNDS FOR IMAGING AND DETECTION
    申请人:PERKINELMER HEALTH SCIENCES, INC.
    公开号:US20190100654A1
    公开(公告)日:2019-04-04
    This disclosure provides a family of compounds that absorb and fluoresce in the short wave infrared region (SWIR, optionally 1000 nm to 1300 nm), including hydrophilic compounds that exhibit absorption and emission spectral profiles in aqueous solutions substantially similar to those observed in organic solvents such as methanol or DMSO. The compounds can be chemically linked to biomolecules including proteins, nucleic acids, and therapeutic small molecules. The compounds are useful for imaging in a variety of medical, biological and diagnostic applications, including SWIR in vivo imaging of regions of interest within a mammal.
    这份披露提供了一类在短波红外区域(SWIR,可选1000纳米至1300纳米)吸收和发射光的化合物家族,包括在溶液中表现出吸收和发射光谱特性与甲醇DMSO等有机溶剂中观察到的基本相似的亲性化合物。这些化合物可以与蛋白质、核酸和治疗性小分子等生物分子化学连接。这些化合物可用于在各种医学、生物学和诊断应用中进行成像,包括对哺乳动物体内感兴趣区域进行SWIR成像。
  • New Near-Infrared Cyanine Dyes for Labelling of Proteins
    作者:Malgorzata Lipowska、Gabor Patonay、Lucjan Strekowski
    DOI:10.1080/00397919308011153
    日期:1993.12
    Abstract Isothiocyanato-functionalized cyanine dyes 7 and 11 for labelling of proteins at amino groups have been synthesized. The dyes and their adducts with amines show strong absorbance and fluorescence in the near-infrared region of 750-850 nm.
    摘要 已经合成了异硫氰酸根合功能化的花青染料 7 和 11,用于标记基上的蛋白质。染料及其与胺的加合物在 750-850 nm 的近红外区域显示出强烈的吸光度和荧光。
  • 신호 대 배경비 향상을 위한 전하 균형 형광 조영제 및 이를 이용한 영상화 방법
    申请人:Pusan National University Industry-University Cooperation Foundation 부산대학교 산학협력단(220040044843) BRN ▼621-82-06530
    公开号:KR20190136341A
    公开(公告)日:2019-12-10
    본 발명은 형광 조영제에 관한 것으로, 구체적으로 영상 유도 수술용 형광 영상 장치를 사용하여 조직 및 세포를 광학적으로 관찰할 때 높은 신호 대 배경 비를 낼 수 있도록 하는 전하 균형 형광 조영제 및 이를 이용한 영상화 방법에 관한 것이다.
    This is the translation of the text into Chinese: 本发明涉及荧光造影剂,具体地涉及使用显微手术用荧光成像装置在光学上观察组织和细胞时,使信号与背景的比值高的电荷平衡荧光造影剂及其图像化方法。
  • [EN] CYANINE DYES AND THEIR CONJUGATES<br/>[FR] COLORANTS À BASE DE CYANINE ET LEURS CONJUGUÉS
    申请人:LI COR INC
    公开号:WO2012054749A1
    公开(公告)日:2012-04-26
    Compounds and methods are disclosed that are useful for noninvasive imaging in the near-infrared spectral range. The cyanine compounds of Formula (I), are presented: wherein Q is a portion of a polymethine bridge selected from the group consisting (Formula (X)). Also included are bioconjugates of the compounds of Formula (I), methods of labeling biomolecules with the compounds, and methods of imaging.
    揭示了用于近红外光谱范围内非侵入性成像的化合物和方法。所述的青菁化合物的化学式(I)如下所示:其中Q是从羧甲纶桥的一部分中选择的,所述羧甲纶桥选自以下群体(化学式(X))。还包括化合物的生物共轭物,用该化合物标记生物分子的方法,以及成像方法。
  • Symmetric, monofunctionalised polymethine dyes labelling reagents
    申请人:Innosense S.r.l.
    公开号:EP1221465A1
    公开(公告)日:2002-07-10
    A symmetric cyanine of the formula: wherein: X is selected from the group consisting of O, S and C(CH3)2; W represents non-metal atoms required to form a benzo-condensed or a naphto-condensed ring; R1 is selected from the group consisting of (CH2)nCH3, (CH2)nSO3- and (CH2)nSO3H, wherein n is an integer selected from 0 to 6 when R1 is (CH2)nCH3, and n is an integer selected from 3 to 6 when R1 is (CH2)nSO3- or (CH2)nSO3H; R2 and R3 are independently selected from the group consisting of H, a sulphonic moiety and a sulphonate moiety; Q is selected from the group consisting of: wherein q is 0 or 1 and D is selected from the group consisting of:         -C≡C-G; and wherein A is O or S and G is, or contains a N, O or S nucleophile moiety or is, or contains a moiety capable of reacting with N, O or S nucleophiles.
    公式为:其中:X从O、S和C(CH3)2组成的组中选择;W代表形成苯并或并环所需的非属原子;R1从(CH2)n 、( )nSO3-和( )nSO3H组成的组中选择,其中当R1为( )n 时,n是从0到6选择的整数,当R1为( )nSO3-或( )nSO3H时,n是从3到6选择的整数;R2和R3独立地从H、磺酸基团和磺酸盐基团组成的组中选择;Q从以下组成的组中选择:其中q为0或1,D从以下组成的组中选择:-C≡C-G;其中A为O或S,G是或含有N、O或S亲核基团,或是或含有能与N、O或S亲核基团发生反应的基团。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫