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5'-Pyrrolidino-2,2'-bithiophene-5-carboxaldehyde | 146823-45-2

中文名称
——
中文别名
——
英文名称
5'-Pyrrolidino-2,2'-bithiophene-5-carboxaldehyde
英文别名
5-(5-Pyrrolidin-1-ylthiophen-2-yl)thiophene-2-carbaldehyde
5'-Pyrrolidino-2,2'-bithiophene-5-carboxaldehyde化学式
CAS
146823-45-2
化学式
C13H13NOS2
mdl
——
分子量
263.384
InChiKey
KRGJLAMAAZFLAB-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):
    3.7
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    76.8
  • 氢给体数:
    0
  • 氢受体数:
    4

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

反应信息

  • 作为反应物:
    描述:
    5'-Pyrrolidino-2,2'-bithiophene-5-carboxaldehyde 在 sodium tetrahydroborate 、 magnesium sulfate 作用下, 以 甲醇甲苯 为溶剂, 反应 40.0h, 生成 (1R,2R)-N,N'-Bis-(5'-pyrrolidin-1-yl-[2,2']bithiophenyl-5-ylmethyl)-cyclohexane-1,2-diamine
    参考文献:
    名称:
    通过催化剂远程分子功能化控制不对称过程的立体化学结果:手性二氨基-低聚噻吩(DAT)作为不对称催化中的配体。
    摘要:
    介绍了新型的高度通用的手性C(2)-对称的二胺-低聚噻吩配体在钯催化的不对称转化中的合成,表征和结构导向的应用。描述了侧挂π-共轭寡聚噻吩在确定相应手性Pd配合物的催化活性中的亲密作用的实验研究。它们的异常行为为通过远程结构功能化对微调有机金属催化剂进行逻辑设计开辟了新的途径。
    DOI:
    10.1002/chem.200500889
  • 作为产物:
    描述:
    参考文献:
    名称:
    Fluorescent Bithiophene Chromophores: Synthesis and Application in CD Exciton Chirality Studies
    摘要:
    DOI:
    10.3987/com-97-s57
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文献信息

  • Amino(oligo)thiophene dyes, preparation thereof, and optical methods of use
    申请人:The University of Connecticut
    公开号:US08129532B2
    公开(公告)日:2012-03-06
    Amino(oligo)thiophene dyes useful for studying the electrophysiology of organelles, cells, and tissues are described. Compared to previously known dyes, the amino(oligo)thiophene dyes exhibit improved (faster) response to membrane potential changes, as well as the ability to be excited by 1064 nanometer femtosecond pulses. Methods of preparing the amino( oligo )thiophene dyes are also described.
    描述了用于研究细胞器、细胞和组织电生理学的氨基(寡)噻吩染料。与先前已知的染料相比,氨基(寡)噻吩染料表现出对膜电位变化的改善(更快)响应,以及能够被1064纳米飞秒脉冲激发的能力。还描述了制备氨基(寡)噻吩染料的方法。
  • AMINO(OLIGO)THIOPHENE DYES, PREPARATION THEREOF, AND OPTICAL METHODS OF USE
    申请人:Loew Leslie M.
    公开号:US20090042227A1
    公开(公告)日:2009-02-12
    Amino(oligo)thiophene dyes useful for studying the electrophysiology of organelles, cells, and tissues are described. Compared to previously known dyes, the amino(oligo)thiophene dyes exhibit improved (faster) response to membrane potential changes, as well as the ability to be excited by 1064 nanometer femtosecond pulses. Methods of preparing the amino(oligo)thiophene dyes are also described.
    描述了用于研究细胞器、细胞和组织电生理学的氨基(寡聚)噻吩染料。与先前已知的染料相比,氨基(寡聚)噻吩染料对膜电位变化的响应更快,并且能够受到1064纳米飞秒脉冲的激发。还描述了制备氨基(寡聚)噻吩染料的方法。
  • Synthesis and Solvatochromic Properties of Donor-Acceptor-Substituted Oligothiophenes
    作者:Franz Effenberger、Frank Wuerthner、Felix Steybe
    DOI:10.1021/jo00112a032
    日期:1995.4
    The Pd-catalyzed cross coupling reaction of electron donor-substituted thiophenes 1 with electron acceptor-substituted halothiophenes 2,10 via organozinc intermediates or organotin compounds 5 to give bi-, ter-, and quaterthiophenes 3, 4, 6, 8, 12, 13, and 14 is described. (Dimethylamino)-bithiophenes 8 with acceptor groups of varying reactivity were prepared via 5d in 60-80% yield, whereas bithiophenes 6d,e were obtained as a mixture with phenylthiophenes 7d,e. Symmetrical substituted byproducts 11 were formed in the conversion of 1b with bromothiophenes 10 via organozinc compounds yielding oligothiophenes 6b and 12. The ter- and quaterthiophenes 13 and 14 were isolated in about 50-70% yield. The electronic interactions between donor and acceptor end groups in the conjugated bithiophenes 3, 4, and 8 are expressed in the intensive and markedly solvatochromic CT transitions. The solvatochromic behavior of 3, 4, and 8 was determined by linear regression analyses of absorption maxima in 11 solvents, whereby bithiophene 3d was found to be a very appropriate indicator dye whose absorption wavenumbers ($) over bar nu(max)(3d) in aliphatic and dipolar aprotic and-on consideration of the polarizability correction term d delta-in aromatic and chlorinated solvents excellently correlate with the pi* values defined by Kamlet and Taft.
  • FLUORESCENT DYE, PREPARATION METHOD AND USES THEREOF
    申请人:FLUORESCENCE DIAGNOSIS (SHANGHAI) BIOTECH COMPANY LTD.
    公开号:US20220214351A1
    公开(公告)日:2022-07-07
    A fluorescent dye, as well as a preparation method and uses thereof, wherein the fluorescent dye is sensitive and specific to viscosity and has low background fluorescence; it can also be used as a fluorescent activated and lighted probe used for fluorescent labeling, quantification or monitoring of protein, enzymes or nucleic acid.
  • US8129532B2
    申请人:——
    公开号:US8129532B2
    公开(公告)日:2012-03-06
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同类化合物

试剂2,2'-Thieno[3,2-b]thiophene-2,5-diylbis-3-thiophenecarboxylicacid 苯并[b]噻吩,3-(2-噻嗯基)- 甲基[2,3'-联噻吩]-5-羧酸甲酯 牛蒡子醇 B 十四氟-Alpha-六噻吩 三丁基(5''-己基-[2,2':5',2''-三联噻吩]-5-基)锡 α-四联噻吩 α-六噻吩 α-五联噻吩 α-七噻吩 α,ω-二己基四噻吩 5,5′-双(3-己基-2-噻吩基)-2,2′-联噻吩 α,ω-二己基六联噻吩 Α-八噻吩 alpha-三联噻吩甲醇 alpha-三联噻吩 [3,3-Bi噻吩]-2,2-二羧醛 [2,2’]-双噻吩-5,5‘-二甲醛 [2,2':5',2''-三联噻吩]-5,5''-二基双[三甲基硅烷] [2,2'-联噻吩]-5-甲醇,5'-(1-丙炔-1-基)- [2,2'-联噻吩]-5-甲酸甲酯 [2,2'-联噻吩]-5-乙酸,a-羟基-5'-(1-炔丙基)-(9CI) C-[2,2-二硫代苯-5-基甲基]胺 5’-己基-2,2’-联噻吩-5-硼酸频哪醇酯 5-辛基-1,3-二(噻吩-2-基)-4H-噻吩并[3,4-c]吡咯-4,6(5H)-二酮 5-苯基-2,2'-联噻吩 5-溴5'-辛基-2,2'-联噻吩 5-溴-5′-己基-2,2′-联噻吩 5-溴-5'-甲酰基-2,2':5'2'-三噻吩 5-溴-3,3'-二己基-2,2'-联噻吩 5-溴-3'-癸基-2,2':5',2''-三联噻吩 5-溴-2,2-双噻吩 5-溴-2,2'-联噻吩-5'-甲醛 5-氯-5'-苯基-2,2'-联噻吩 5-氯-2,2'-联噻吩 5-正辛基-2,2'-并噻吩 5-己基-5'-乙烯基-2,2'-联噻吩 5-己基-2,2-二噻吩 5-全氟己基-5'-溴-2,2'-二噻吩 5-全氟己基-2,2′-联噻吩 5-乙酰基-2,2-噻吩基 5-乙氧基-2,2'-联噻吩 5-丙酰基-2,2-二噻吩 5-{[[2,2'-联噻吩]-5-基}噻吩-2-腈 5-[5-(5-己基噻吩-2-基)噻吩-2-基]噻吩-2-羧酸 5-(羟甲基)-[2,2]-联噻吩 5-(噻吩-2-基)噻吩-2-甲腈 5-(5-甲酰基-3-己基噻吩-2-基)-4-己基噻吩-2-甲醛 5-(5-甲基噻吩-2-基)噻吩-2-甲醛 5-(5-噻吩-2-基噻吩-2-基)噻吩-2-羧酸 5-(5-乙炔基噻吩-2-基)噻吩-2-甲醛