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Ethyl-acetimidothioat-hydrochlorid | 5426-05-1

中文名称
——
中文别名
——
英文名称
Ethyl-acetimidothioat-hydrochlorid
英文别名
ethyl acetothioimidate hydrochloride;Ethyl Thioethanimidate Hydrochloride;S-ethyl thioacetamide hydrochloride;thioacetimidic acid ethyl ester; hydrochloride;Thioacetimidsaeure-aethylester; Hydrochlorid;Ethyl ethanimidothioate--hydrogen chloride (1/1);ethyl ethanimidothioate;hydrochloride
Ethyl-acetimidothioat-hydrochlorid化学式
CAS
5426-05-1
化学式
C4H9NS*ClH
mdl
——
分子量
139.649
InChiKey
HSQRFYVSCJJFEU-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):
    2.16
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    49.2
  • 氢给体数:
    2
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2930909090

SDS

SDS:a34f09970351a94a78eb953ce3e243d9
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反应信息

  • 作为反应物:
    描述:
    Ethyl-acetimidothioat-hydrochlorid盐酸羟胺sodium methylate 作用下, 以 乙醇氯仿 为溶剂, 反应 1.0h, 以55%的产率得到S-ethyl-N-hydroxyacetimidate
    参考文献:
    名称:
    Bansal, Journal of the Indian Chemical Society, 2004, vol. 81, # 11, p. 968 - 971
    摘要:
    DOI:
  • 作为产物:
    描述:
    乙腈乙硫醇盐酸 作用下, 反应 96.0h, 以75%的产率得到Ethyl-acetimidothioat-hydrochlorid
    参考文献:
    名称:
    Bansal, Journal of the Indian Chemical Society, 2004, vol. 81, # 11, p. 968 - 971
    摘要:
    DOI:
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文献信息

  • Zur Chemie der 1,2,4-Triazine; XIII<sup>1</sup>. Synthese von 1<i>H</i>-[1,2,4] Triazino[5,6-<i>e</i>][1,3,4]thiadiazinen und 1,2,4-Triazolo[4,3-<i>d</i>][1,2,4]triazinen
    作者:Hans Neunhoeffer、Marita Dostert、Heinz Hammann
    DOI:10.1055/s-1988-27705
    日期:——
    Chemistry of 1,2,4-Triazines; XIII. Synthesis of 1H-[1,2,4]Triazino [5,6-e][1,3,4]thiadiazines and 1,2,4-Triazolo[4,3-d][1,2,4]triazines The reaction of 6-amino-5-hydrazino-1,2,4-triazines with (thioacylthio)acetic acids affords 6-amino-5-(N 2-thioacylhydrazino)-1,2,4-triazines while the reaction with ethyl dithioacetate yields 8-amino-1,2,4-triazolo[4,3-d] [1,2,4]triazines. The 6-amino-5-(N 2-thioacylhydrazino)-1,2,4-triazines cyclize in aqueous mineral acid to give 1H-[1,2,4]triazino [5,6-e] [1,3,4]thiadiazines. Some further reactions of 5-hydrazino-1,2,4-triazines are reported.
    1,2,4-三嗪的化学;XIII.合成 1H-[1,2,4]三嗪并[5,6-e][1,3,4]噻二嗪和 1,2,4-三唑并[4,3-d][1,2,4]三嗪 6-amino-5-hydrazino-1,2、4-三嗪与(硫代乙酰硫)乙酸反应生成 6-氨基-5-(N 2-硫代乙酰肼)-1,2,4-三嗪,而与二硫代乙酸乙酯反应则生成 8-氨基-1,2,4-三唑并[4,3-d][1,2,4]三嗪。6- 氨基-5-(N 2-硫代酰基肼)-1,2,4-三嗪在矿酸水溶液中环化,生成 1H-[1,2,4]三嗪并[5,6-e] [1,3,4]噻二嗪。报告还介绍了 5-肼基-1,2,4-三嗪的一些进一步反应。
  • 2-β-d-ribofuranosylbenzoxazole from 2,5-anhydro-d-allonoimidate, and 1,3-dimethyl-8-β-d-ribofuranosylxanthine from 2,5-anhydro-d-allono-thioimidates and -dithioates
    作者:Hassan S. El Khadem、Joshua Kawai
    DOI:10.1016/s0008-6215(00)90269-6
    日期:1986.10
  • An Improved Preparation of Dithioesters and Some Reactions and Spectral Properties of These Compounds
    作者:C. S. Marvel、P. de Radzitzky、James J. Brader
    DOI:10.1021/ja01627a060
    日期:1955.11
  • Weygand,F. et al., Chemische Berichte, 1962, vol. 95, p. 2264 - 2269
    作者:Weygand,F. et al.
    DOI:——
    日期:——
  • Schmidt,E., Chemische Berichte, 1914, vol. 47, p. 2547
    作者:Schmidt,E.
    DOI:——
    日期:——
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同类化合物

替莫美他汀 乙酰亚胺基硫酸,甲基酯 5-甲基四氢噻吩-2-亚胺盐酸盐 4-[(1E,5E,7E,11R)-11-甲氧基十四碳-1,5,7,13-四烯基]-2-(2-甲基环丙基)-4,5-二氢-1,3-噻唑 2-环戊基-4,5-二氢-1,3-噻唑 2-氧代丙基乙烷硫代亚氨酸酯 2-亚氨基硫烷盐酸盐 2-亚氨基硫杂环戊烷 2-亚氨基-5-甲基-3-(3-氧代丁基)四氢-3-噻吩甲腈 2-亚氨基-4-氧代四氢-3-噻吩羧酸 2-亚氨基-2-(甲基硫代)乙酸乙酯 2-亚氨基-2,3-二氢-噻吩 1-[5-(甲硫基)-3,4-二氢-2H-吡咯-3-基]乙酮 (S)-5-乙基-2-硫代甲基-1-吡咯啉 (4R)-4-[(1Z,5E,7E,11R)-11-甲氧基-8-甲基十四碳-1,5,7,13-四烯基]-2-[(1R,2S)-2-甲基环丙基]-4,5-二氢-1,3-噻唑 (3,6-二碘噻吩并[3,2-b]噻吩e-2,5-二亚基)二氰胺 ethyl [2-(tiophen-2-yl)-4,5-dihydrothiazol-5-yl]acetate 6-amino-3-carbamoyl-2-carbethoxymethylthio-5-cyano-3,4-dihydrospirocyclohexane-4-pyridine 2-allylthio-6-amino-3-carbamoyl-5-cyano-3,4-dihydrospirocyclohexane-4-pyridine N-<1-(4,5-Dihydro-1,3-thiazol-2-yl)cyclopentyl>-N',N'-dimethylthioharnstoff 2-methylthio-4'-oxo-5,5-pentamethylenespiro[1'-pyrroline-3,1'-cyclohexadiene] 2',6'-dimethoxy-5,5-dimethyl-2-methylthio-4'-oxospiro(1-pyrrolin-3,1'-cyclohexadiene) 2-(methylthio)-1-azetine 2-imino-tetrahydro-thiophene-3-carboxylic acid ethyl ester 4-Methyl-N-(2-vinyloxy-ethyl)-penta-2,3-dienimidothioic acid methyl ester N-ethyl-2-ethylsulfanyl-1-methylsulfanyl-2-propen-1-imine 8-(ethylthio)-6-methyl-7-azabicyclo<4.2.0>octa-3,7-diene 3,3,7-trimethyl-1-methylthio-2-azaspiro[4.5]deca-1,6,9-trien-8-one 1,1-dimethyl-4-methylsulfanyl-1,5-diazapentadiene hydriodide N-methyl-2-ethoxy-1-methylsulfanyl-2-propen-1-imine 7-hydroxy-6,9-dimethoxy-3-methyl-1-methylsulfanyl-2-azaspiro[4.5]deca-1,6,9-trien-8-one 19S-curacin A 15,16-dihydrocuracin A curacin B 2-Methoxy-N-(2-vinyloxy-ethyl)-buta-2,3-dienimidothioic acid methyl ester N-methyl-2-ethylsulfanyl-1-methylsulfanyl-2-propen-1-imine N-(tert-Butoxycarbonyl)-glycyl-glycin-imidthiosaeure-S-ethylester Methyl propanimidothioate;hydrochloride 2,2-dimethyl-4-methylthio-3-thiazoline methyl 2-methoxy-N-methyl-2,3-butadienimidothioate 4-(2-bromopropan-2-yl)-4,5-dihydro-2,4'-bithiazole 2-(Cyclopropyl)-2-thiazolin 5.5'-Dimethyl-2.2'-bi-2-thiazolin 4-chloromethyl-2-thiophen-2-yl-4,5-dihydro-thiazol-4-ol 5,5-dimethyl-2-iminothiolane hydrochloride N-(3-methyl-2-thietanylidene)isopropylamine Aethyl-N-vinylformimidat thioacetimidic acid butyl ester; hydrochloride tert-butyl (4S)-4-[(4S)-4-cyano-4-methyl-5H-1,3-thiazol-2-yl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate Ethyl-thioacetamidat