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N,N'-二异丁基硫脲 | 29214-81-1

中文名称
N,N'-二异丁基硫脲
中文别名
N,N’-二异丁基硫脲;N,N`-二异丁基硫脲
英文名称
N,N'-diisobutylthiourea
英文别名
1,3-di(isobutyl)thiourea;N,N'-Diisobutyl-thioharnstoff;N,N'-Di-i-butylthioharnstoff;Urea, 1,3-diisobutyl-2-thio-;1,3-bis(2-methylpropyl)thiourea
N,N'-二异丁基硫脲化学式
CAS
29214-81-1
化学式
C9H20N2S
mdl
MFCD00015042
分子量
188.337
InChiKey
YFIXICPADGNMGZ-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:
    240.7±23.0 °C(Predicted)
  • 密度:
    0.939±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.888
  • 拓扑面积:
    56.2
  • 氢给体数:
    2
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2930909090

SDS

SDS:9e086d9a7c627c3b4d57b4dea3624253
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反应信息

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文献信息

  • Cis-Trans Isomerism in Square Planar [TeX 2 (stu) 2 ] Complexes (X = Br − , I − ) with Bulky Substituted Thiourea (stu) Ligands. Syntheses and Structures of Four New Tellurium(II) Complexes
    作者:Steinar Husebye、Dima Mughannam、Karl W. Törnroos
    DOI:10.1080/10426500307833
    日期:2003.8.1
    9639 Å, reflecting the stronger trans influences of the two thioureas as compared to that of bromide. In 3 and 4 where there is no trans influence affecting the Te-ligand bonds, the average Te-S and Te-I bond lengths are 2.6926 and 2.9761 Å respectively. Tetraalkyl- or arylsubstituted thioureas alone as well as bulky disubstituted thioureas together with I m ligands seem to favor formation of trans
    通过将适当取代的硫脲在 MeOH(Br m 络合物)或 DMF(1 m 络合物)中的热溶液添加到溶解在热浓中的 TeO 2 溶液中来合成络合物。盐酸。所得四坐标方形平面配合物的结构,顺式 -[TeBr 2 ( i PrNH) 2 CS} 2 ] ( 1 ),顺式 -[TeBr 2 ( i BuNH) 2 CS} 2 ] ( 2 ),反式-[TeI 2 ( i PrNH) 2 CS} 2 ] ( 3 ) 和反式-[TeI 2 ( i BuNH) 2 CS} 2 ] ( 4 ),通过X 射线晶体学方法进行了研究。1 和 2 中的平均 Te-S 键长为 2.5364 Å。相应的平均 Te-Br 键长为 2.9639 Å,反映了与溴化物相比,两种硫脲的反式影响更强。在没有影响 Te-配体键的反式影响的 3 和 4 中,平均 Te-S 和 Te-I 键长分别为 2.6926 和 2.9761
  • Thiazolidine derivatives
    申请人:Hoechst Aktiengesellschaft
    公开号:US04061761A1
    公开(公告)日:1977-12-06
    The invention relates to thiazolidine derivatives having in 4-position a hydroxy group and a 3'-sulphamyl-phenyl substituent, in 2-position an imino group and in 1-position an aliphatic or cycloaliphatic substituent. Said thiazolidines have diuretic activity. The invention also relates to a process for the manufacture of said compounds.
    本发明涉及在4位具有羟基和3'-磺酰氨基-苯基取代基,在2位具有亚氨基,在1位具有脂肪族或环脂肪族取代基的噻唑烷衍生物。所述噻唑烷具有利尿活性。本发明还涉及制造所述化合物的方法。
  • Synthesis, Crystal Structure, and DFT Calculations of 1,3-Diisobutyl Thiourea
    作者:Ataf A. Altaf、Adnan Shahzad、Zarif Gul、Sher A. Khan、Amin Badshah、Muhammad N. Tahir、Zafar I. Zafar、Ezzat Khan
    DOI:10.1155/2015/913435
    日期:——

    1,3-Diisobutyl thiourea was synthesized and characterized by single crystal X-ray diffraction. It gives a monoclinic (α=γ= 90 andβ  90) structure with the space group P21/c. The unit cell dimensions area= 11.5131 (4) Å,b= 9.2355 (3) Å,c= 11.3093 (5) Å,α= 90°,β= 99.569° (2),γ= 90°,V= 1185.78 (8) Å3, andZ= 4. The crystal packing is stabilized by intermolecular (N–H⋯S) hydrogen bonding in the molecules. The optimized geometry and Mullikan's charges of the said molecule calculated with the help of DFT using B3LYP-6-311G model support the crystal structure.

    1,3-二异丁基硫脲已通过单晶X射线衍射进行了合成和表征。它给出了一个单斜晶系(α=γ=90°和β≠90°)结构,空间群为P21/c。晶胞尺寸为a=11.5131(4)Å,b=9.2355(3)Å,c=11.3093(5)Å,α=90°,β=99.569°(2),γ=90°,V=1185.78(8)ų,Z=4。晶体堆积是通过分子间(N–H…S)氢键稳定的。使用B3LYP-6-311G模型通过DFT计算出的所述分子的优化几何结构和Mullikan电荷支持了晶体结构。
  • A CONVENIENT METHOD FOR THE PREPARATION OF N,N′-DISUBSTITUTED THIOUREAS USING 2-CHLOROPYRIDINIUM SALT, SODIUM TRITHIOCARBONATE AND AMINES
    作者:Yuji Takikawa、Noriyuki Inoue、Ryu Sato、Saburo Takizawa
    DOI:10.1246/cl.1982.641
    日期:1982.5.5
    N,N-Disubstituted thioureas were prepared in high yields by treating 2-chloropyridinium salt with sodium trithiocarbonate and subsequently adding amines.
    N,N'-二取代硫脲通过用三硫代碳酸钠处理 2-氯吡啶鎓盐并随后加入胺以高产率制备。
  • FUNCTIONALIZED HIGHLY BRANCHED MELAMINE-POLYAMINE POLYMERS
    申请人:Peretolchin Maxim
    公开号:US20120252987A1
    公开(公告)日:2012-10-04
    The present invention relates to a method for producing amphiphilic functionalized highly branched melamine-polyamine polymers by condensing melamine and optionally a melamine derivate having at least one different amine having at least two primary amino groups and optionally also with urea and/or at least one urea derivative and/or with at least one at least difunctional diisocyanate or polyisocyanate and/or at least one carbolic acid having at least two carboxyl groups or at least one derivative thereof, optionally quaternizing a portion of the amino groups of the polymer thereby obtained, reacting the polymer thus obtained with at least one compound capable of undergoing a condensation or addition reaction with amino groups, and optionally quaternizing at least part of the amino groups of the polymer obtained in the first step. The invention further relates to the amphiphilic functionalized highly branched melamine-polyamine polymers that can be obtained by the method according to the invention, and to the use thereof as surface active agents.
    本发明涉及一种通过将三聚氰胺和至少一种具有至少两个主要氨基的不同氨基的三聚氰胺衍生物以及可能还包括尿素和/或至少一种尿素衍生物和/或至少一种至少双官能团二异氰酸酯或多异氰酸酯和/或至少一种至少具有两个羧基的羧酸或其衍生物缩合,从而制备含有两性功能化的高支化三聚氰胺-多胺聚合物的方法。可选地,对所获得的聚合物的部分氨基进行季铵化,然后将所获得的聚合物与至少一种能够与氨基发生缩合或加成反应的化合物反应,并可选地对第一步中获得的聚合物的部分氨基进行季铵化。本发明还涉及通过本发明的方法可以获得的含有两性功能化的高支化三聚氰胺-多胺聚合物,以及将其用作表面活性剂的用途。
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