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5-tert-butyl-2,2':5',2''-terthienyl | 118824-84-3

中文名称
——
中文别名
——
英文名称
5-tert-butyl-2,2':5',2''-terthienyl
英文别名
2-Tert-butyl-5-(5-thiophen-2-ylthiophen-2-yl)thiophene
5-tert-butyl-2,2':5',2''-terthienyl化学式
CAS
118824-84-3
化学式
C16H16S3
mdl
——
分子量
304.501
InChiKey
DBBDFTHFZHTDQS-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

物化性质

  • 沸点:
    401.9±45.0 °C(Predicted)
  • 密度:
    1.193±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.1
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    84.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2-叔丁基噻吩 、 5-iodo-2,2'-bithiophene 在 [1,3-bis(diphenylphosphino)propane]nickel(II) dichloride 正丁基锂 、 magnesium bromide 作用下, 生成 5-tert-butyl-2,2':5',2''-terthienyl
    参考文献:
    名称:
    Synthesis and characterization of alkyl-, halo- and hetero-substituted derivatives of the potent phototoxin α-terthienyl
    摘要:
    DOI:
    10.1016/s0040-4020(01)81692-6
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文献信息

  • Oligonucleotide compositions and methods thereof
    申请人:WAVE LIFE SCIENCES LTD.
    公开号:US10479995B2
    公开(公告)日:2019-11-19
    Among other things, the present disclosure relates to chirally controlled oligonucleotides of select designs, chirally controlled oligonucleotide compositions, and methods of making and using the same. In some embodiments, a provided chirally controlled oligonucleotide composition provides different cleavage patterns of a nucleic acid polymer than a reference oligonucleotide composition. In some embodiments, a provided chirally controlled oligonucleotide composition provides single site cleavage within a complementary sequence of a nucleic acid polymer. In some embodiments, a chirally controlled oligonucleotide composition has any sequence of bases, and/or pattern or base modifications, sugar modifications, backbone modifications and/or stereochemistry, or combination of these elements, described herein.
    除其他外,本公开涉及选择设计的手性控制寡核苷酸、手性控制寡核苷酸组合物以及制造和使用方法。在一些实施方案中,所提供的手性控制寡核苷酸组合物提供了与参考寡核苷酸组合物不同的核酸聚合物裂解模式。在一些实施方案中,所提供的手性控制寡核苷酸组合物在核酸聚合物的互补序列内提供单位点裂解。在一些实施方案中,手性控制寡核苷酸组合物具有本文所述的任何碱基序列和/或模式或碱基修饰、糖修饰、骨架修饰和/或立体化学,或这些元素的组合。
  • Metal-based coordination complexes as photodynamic compounds and their use
    申请人:McFarland Sherri Ann
    公开号:US10766915B2
    公开(公告)日:2020-09-08
    Compositions of the invention include metal-based coordination complexes, which are preferably tunable photodynamic compounds. The compositions and complexes are useful as therapeutic agents and as in vivo diagnostic agents for treating or preventing diseases including those that involve hyperproliferating cells in their etiology, such as cancer. Compositions and complexes of the invention are further capable of destroying microbial cells, such as bacteria, fungi, and protozoa, and destroying viruses. The compositions and complexes are also capable of modulating cell function in other ways.
    本发明的组合物包括金属基配位复合物,它们最好是可调光动力化合物。本发明的组合物和配合物可用作治疗剂和体内诊断剂,用于治疗或预防疾病,包括在病因中涉及细胞过度增殖的疾病,如癌症。本发明的组合物和复合物还能消灭微生物细胞,如细菌、真菌和原生动物,并能消灭病毒。本发明的组合物和复合物还能以其他方式调节细胞功能。
  • Oligonucleotides, compositions and methods thereof
    申请人:WAVE LIFE SCIENCES LTD.
    公开号:US11013757B2
    公开(公告)日:2021-05-25
    The present disclosure pertains to the recognition that immune responses mediated by CpG oligonucleotides can be affected by the stereochemistry of modified internucleotidic linkages such as phosphorothioates. In some embodiments, the present disclosure relates to chirally controlled CpG oligonucleotide compositions comprising CpG oligonucleotides comprising multiple modified internucleotidic linkages such as phosphorothioate linkages, wherein the oligonucleotides comprise one or more CpG region motifs having defined stereochemistry patterns of chiral internucleotidic linkages. In some embodiments, CpG oligonucleotides comprising one or more CpG region motifs are capable of agonizing an immune response. In some embodiments, CpG oligonucleotides comprising one or more CpG region motifs are antagonistic. Methods for making and using chirally controlled CpG oligonucleotide compositions are also described. In some embodiments, no immune modulation is desired, and the present disclosure provides methods of identifying chirally controlled oligonucleotide compositions which have decreased immune modulation.
    本公开涉及这样一种认识,即 CpG 寡核苷酸介导的免疫反应可受硫代磷酸酯等修饰的核苷酸间连接的立体化学的影响。在一些实施方案中,本公开涉及手性控制的 CpG 寡核苷酸组合物,该组合物包含CpG 寡核苷酸,该CpG 寡核苷酸包含多个修饰的核苷酸间连接,如硫代磷酸酯连接,其中寡核苷酸包含一个或多个 CpG 区域基序,该 CpG 区域基序具有手性核苷酸间连接的确定立体化学模式。在一些实施方案中,包含一个或多个 CpG 区域基团的 CpG 寡核苷酸能够激动免疫反应。在某些实施方案中,包含一个或多个 CpG 区域基团的 CpG 寡核苷酸具有拮抗作用。还描述了制作和使用啁啾控制 CpG 寡核苷酸组合物的方法。在某些实施方案中,不需要免疫调节,本公开提供了确定免疫调节性降低的手性控制寡核苷酸组合物的方法。
  • EACHERN, ANITA MAC;SOUCY, CHANTAL;LEITCH, LEONARD C.;ARNASON, JOHN T.;MOR+, TETRAHEDRON, 44,(1988) N 9, 2403-2412
    作者:EACHERN, ANITA MAC、SOUCY, CHANTAL、LEITCH, LEONARD C.、ARNASON, JOHN T.、MOR+
    DOI:——
    日期:——
  • METAL-BASED COORDINATION COMPLEXES AS PHOTODYNAMIC COMPOUNDS AND THEIR USE
    申请人:MCFARLAND Sherri Ann
    公开号:US20160039854A1
    公开(公告)日:2016-02-11
    Compositions of the invention include metal-based coordination complexes, which are preferably tunable photodynamic compounds. The compositions and complexes are useful as therapeutic agents and as in vivo diagnostic agents for treating or preventing diseases including those that involve hyperproliferating cells in their etiology, such as cancer. Compositions and complexes of the invention are further capable of destroying microbial cells, such as bacteria, fungi, and protozoa, and destroying viruses. The compositions and complexes are also capable of modulating cell function in other ways.
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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