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Ethyl 2-[(thiophen-2-yl)methylidene]hydrazine-1-carbodithioate | 213892-47-8

中文名称
——
中文别名
——
英文名称
Ethyl 2-[(thiophen-2-yl)methylidene]hydrazine-1-carbodithioate
英文别名
ethyl N-(thiophen-2-ylmethylideneamino)carbamodithioate
Ethyl 2-[(thiophen-2-yl)methylidene]hydrazine-1-carbodithioate化学式
CAS
213892-47-8
化学式
C8H10N2S3
mdl
——
分子量
230.379
InChiKey
OEVVNCJXZXPXHM-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:
    347.2±34.0 °C(Predicted)
  • 密度:
    1.28±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    110
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Reactions of Hydrazonoyl Halides 56<sup>1</sup>: Synthesis and Reactions of 1-Bromo-2-(5-chloro-benzofuranyl)ethanedione-1-phenylhydrazone
    作者:Abdou O. Abdelhamid、Ahmed H El-Ghandour、Ahmed A.M. El-Reedy
    DOI:10.1080/10426500701640876
    日期:2008.4.18
    2,3-Dihydro-1,3,4-thiadiazoles and triazolino[4,3-a]pyrimidines containing benzofuran moiety were prepared from reaction of 1-bromo-2-(5-chlorobenzofuranyl) ethanedione-1-phenylhydrazone with each of potassium thiocyanate, alkyl carbodithioates and pyrmidine-2-thiones. All newly synthesized were confirmed by elemental analysis, spectral data, and alternative route synthesis whenever possible.
    含有苯并呋喃部分的 2,3-二氢-1,3,4-噻二唑和三唑并[4,3-a]嘧啶是由 1--2-(5-氯苯并呋喃基)乙二酮-1-苯腙与每一种反应制备的硫氰酸钾、烷基碳二代酸酯和嘧啶-2-酮。所有新合成的都尽可能通过元素分析、光谱数据和替代路线合成进行确认。
  • REACTIONS WITH HYDRAZONOYL HALIDES XXIV<sup>[1]</sup>: SYNTHESIS OF SOME NEW UNSYMMETRICAL AZINES AND DIHYDRO-1,3,4-THIADIAZOLES
    作者:Abdou O. Abdelhamid、Gaber S. Mohamed
    DOI:10.1080/10426509908031623
    日期:1999.9.1
    Abstract Unsymmetrical azines were synthesized from reaction of C-coumarinoyl-N-arylformohydrazonoyl bromide with different alkyl carbodithioates. In addition, reactions of hydrazonoyl halides with thioanilide and methyl dithioates were studied. The structures of newly synthesized compounds were confirmed by elemental analyses, spectroscopic tools, and alternative syntheses whenever possible.
    摘要 C-香豆素酰-N-芳基甲腙酰与不同的碳二代烷基酯反应合成了不对称吖嗪。此外,还研究了腙酰卤苯胺和二代甲酯的反应。新合成化合物的结构通过元素分析、光谱工具和替代合成尽可能得到确认。
  • Reactions with Hydrazonoyl Halides XXX: Synthesis of Some 2,3-Dihydro-1,3,4-Thiadiazoles and Unsymmetrical Azines Containing Benzothiazole Moiety
    作者:Abdou O. Abdelhamid、Nora M. Rateb、Kamal M. Dawood
    DOI:10.1080/10426500008082403
    日期:2000.1.1
    to give 2,3-dihydro-1,3,4-thiadiazoles in good yields. In contrast, hydrazonoyl bromides react with each of phenylthiourea (19a), phenylthiosemicarbazide (19b), and benzoylthiosemicarbazide (19c) afforded 5-arylazothiazole 22–24(a-c) derivatives, respectively. Structures of the new compounds were elucidated on the basis of elemental analyses, spectral data, and alternative methods of synthesis whenever
    摘要 C-苯并噻唑酰-N-芳基腙酰化物 1a,b 与 2-噻唑基亚甲基碳二代甲酯 (2)、碳二代烷基酯 8-10 和氨基甲酸甲酯 14a-c 在三乙胺存在下反应,得到 2,3 -二氢-1,3,4-噻二唑,收率良好。相比之下,腙酰分别与苯基硫脲 (19a)、苯基硫脲 (19b) 和苯甲酰 (19c) 反应,分别得到 5-芳基偶氮噻唑 22-24(ac) 衍生物。新化合物的结构是在元素分析、光谱数据和其他可能的合成方法的基础上阐明的。
  • 1,3,4-Thia- and -selenadiazole and 1,2,4-triazolo[4,3-a]pyrimidine derivatives from hydrazonoyl halides
    作者:Nadia A. Abdel-Riheem、Nora M. Rateb、Ali A. Al-Atoom、Abdou O. Abdelhamid
    DOI:10.1002/hc.10156
    日期:——
    1,2,4-Triazolo[4,3-a]pyrimidines, thiadiazolines, selenadiazolines, and unsymmetrical azines were synthesized via reactions of a 4-isopropylbenzoyl bromide 4-nitrophenylhydrazone with each of potassium thiocyanate, potassium selenocyanate, ethyl 6-methyl-4-[4-(methylethyl)phenyl]-2-methylthio-3,4-dihydropyrimidine-5-carboxylate, and alkyl carbodithioate. © 2003 Wiley Periodicals, Inc. Heteroatom Chem
    1,2,4-三唑并[4,3-a]嘧啶噻二唑啉、二唑啉和不对称吖嗪通过 4-异丙基苯甲酰溴 4-硝基苯腙与硫氰酸钾硒氰酸钾、6-甲基乙基4-[4-(甲基乙基)苯基]-2-甲基-3,4-二氢嘧啶-5-羧酸酯和碳二代烷基酯。© 2003 Wiley Periodicals, Inc. 杂原子化学 14:421–426, 2003; 在线发表于 Wiley InterScience (www.interscience.wiley.com)。DOI 10.1002/hc.10156
  • Reactions With Hydrazonoyl Halides 59: Synthesis and Antimicrobial Activity of 2,3-Dihydro-1,3,4-thiadiazole, Triazolino[4,3-<i>a</i>]pyrimidine, and Pyrimido[1,2-<i>b</i>][1,2,4,5]tetrazin-6-one Containing Benzofuran Moiety
    作者:Abdou O. Abdelhamid、Mahmoud A. Mohamed、Yasser H. Zaki
    DOI:10.1080/10426500701734265
    日期:2008.6.9
    2,3-Dihydro-1,3,4-thiadiazole, triazolino[4,3-a]pyrimidine and pyrimido[1,2-b][1,2,4,5]tetrazin-6-one containing benzofuran Moiety were synthesized from C-benzofuran-2-yl-N-phenylhydrazonoyl bromides, and the appropriate alkyl arylidenehydrazinecabodithioates and pyrimidine-2-thione and N-aminopyrimidine-2-thione, respectively. All structures of the newly synthesized compounds were elucidated by elemental
    含有苯并呋喃部分的 2,3-二氢-1,3,4-噻二唑、三唑并[4,3-a]嘧啶嘧啶并[1,2-b][1,2,4,5]四嗪-6-酮是分别由 C-苯并呋喃-2-基-N-苯基腙酰和适当的烷基亚芳基代酯和嘧啶-2-酮和N-氨基嘧啶-2-酮合成。新合成的化合物的所有结构都尽可能通过元素分析、光谱数据和替代合成方法阐明。新化合物能够高度抑制细菌(革兰氏阳性和革兰氏阴性)的生长。
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