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S-tertbutylisothiourea hydrochloride | 116727-26-5

中文名称
——
中文别名
——
英文名称
S-tertbutylisothiourea hydrochloride
英文别名
2-tert-butyl-isothiourea; hydrochloride;S-tert-butyl-isothiourea; hydrochloride;S-tert-Butyl-isothioharnstoff; Hydrochlorid;Tert-butyl carbamimidothioate;hydrochloride;tert-butyl carbamimidothioate;hydrochloride
S-tertbutylisothiourea hydrochloride化学式
CAS
116727-26-5
化学式
C5H12N2S*ClH
mdl
——
分子量
168.691
InChiKey
RAIGZUOONQIKSI-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):
    -3.4
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    76.9
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    S-tertbutylisothiourea hydrochloride草酰氯N,N-二异丙基乙胺间氯过氧苯甲酸 作用下, 以 二氯甲烷 为溶剂, 生成 4-(2-Methyl-propane-2-sulfinyl)-[1,3,5]triazin-2-ylamine
    参考文献:
    名称:
    A facile preparation of a combinatorial library of 2,6-disubstituted triazines
    摘要:
    Thiouronium salts of type 3 as dinucleophiles are excellent precursors for the synthesis of various heterocycles in combination through cyclization with a large variety of electrophiles. Using this strategy, 2,6-disubstituted-[l,3,5] triazines of types 4 and 6 have been prepared in good yields. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(98)01164-2
  • 作为产物:
    描述:
    参考文献:
    名称:
    Sprague; Johnson, Journal of the American Chemical Society, 1937, vol. 59, p. 1839
    摘要:
    DOI:
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文献信息

  • Synthesis of Polysubstituted Pyrimidines from Ketene Dithioacetals Using KF/Al<sub>2</sub>O<sub>3</sub>Catalyst
    作者:Shen-Yi Yu、Ya-Xian Cai
    DOI:10.1081/scc-120026325
    日期:2003.12
    Abstract KF/Al2O3 was first used to catalyze the synthesis of 2-alkylthio-4- amino-5-cyano-6-methylthiopyrimidines 3a–f via the reaction of the ketene dithioacetals 1 (prepared from malononitrile) with isothiuronium salts 2a–f. Six pyrimidine compounds were prepared and all of their structures were confirmed by elemental analysis, 1H NMR, and IR. The reaction conditions (solvents, catalyst amounts
    摘要 KF/Al2O3 首次用于通过乙烯酮二硫代缩醛 1(由丙二腈制备)与异硫脲鎓盐 2a-f 的反应催化合成 2-烷硫基-4-氨基-5-氰基-6-甲基硫代嘧啶 3a-f。制备了六种嘧啶化合物,所有结构均通过元素分析、1H NMR 和 IR 确证。首次研究了反应条件(溶剂、催化剂用量和温度)。分离收率达到89%。
  • Investigations on Organo–Sulfur–Nitrogen Rings and the Thiocyanogen Polymer, (SCN)x
    作者:W. Russell Bowman、Colin J. Burchell、Petr Kilian、Alexandra M. Z. Slawin、Philip Wormald、J. Derek Woollins
    DOI:10.1002/chem.200501528
    日期:2006.8.16
    for 1,2,4-thiadiazole and 1,2,4-dithiazole compounds. Peaks in the Raman spectrum in the range 400-480 cm(-1) support the presence of disulfide units within the polymer. The solid-state (13)C NMR (99 % (13)C-labelled) spectrum is dominated by two singlets of equal intensity at approximately 187 and 184 ppm with low intensity peaks in the range 152-172 ppm, in approximately the same range as both 1,2
    报道了一系列1,2,4-噻二唑的合成和完整表征。(SCN)(x)已通过多种技术进行了研究,并将数据与1,2,4-噻二唑和1,2,4-二噻唑进行了比较。观察到的数据表明该聚合物由被氮原子连接的1,2,4-二噻唑环组成。对于(SCN)(x),MALDI-TOF质谱显示在1149处有一个母离子和一系列带有(SCN)(2)重复单元(116 m / z)的峰。该结果暗示(SCN)(2)可以是聚合物的单体单元。它的红外光谱显示一个非常宽的峰,最大峰在1134 cm(-1)处,与1,2,4-噻二唑和1,2,4-二噻唑化合物的环振动在同一区域中包含多个重叠峰。拉曼光谱在400-480 cm(-1)范围内的峰支持聚合物中二硫键单元的存在。固态(13)C NMR(99%(13)C标记)光谱由强度大约在187和184 ppm的两个等强度的单重态占据主导,且强度峰值在152-172 ppm范围内,大致相同范围包括1
  • Goerdeler,J.; Budnowski,M., Chemische Berichte, 1961, vol. 94, p. 1682 - 1688
    作者:Goerdeler,J.、Budnowski,M.
    DOI:——
    日期:——
  • US4129584A
    申请人:——
    公开号:US4129584A
    公开(公告)日:1978-12-12
  • A facile preparation of a combinatorial library of 2,6-disubstituted triazines
    作者:T. Masquelin、Y. Delgado、V. Baumlé
    DOI:10.1016/s0040-4039(98)01164-2
    日期:1998.8
    Thiouronium salts of type 3 as dinucleophiles are excellent precursors for the synthesis of various heterocycles in combination through cyclization with a large variety of electrophiles. Using this strategy, 2,6-disubstituted-[l,3,5] triazines of types 4 and 6 have been prepared in good yields. (C) 1998 Elsevier Science Ltd. All rights reserved.
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