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1,4-dibutyl-2,2-dimethyl-3,5-dioxo-1,4,2-diazaphospholidin-2-ium iodide | 1220345-85-6

中文名称
——
中文别名
——
英文名称
1,4-dibutyl-2,2-dimethyl-3,5-dioxo-1,4,2-diazaphospholidin-2-ium iodide
英文别名
1,4-dibutyl-2,2-dimethyl-1,4,2-diazaphospholidin-2-ium-3,5-dione;iodide
1,4-dibutyl-2,2-dimethyl-3,5-dioxo-1,4,2-diazaphospholidin-2-ium iodide化学式
CAS
1220345-85-6
化学式
C12H24N2O2P*I
mdl
——
分子量
386.213
InChiKey
MXCMSIYDLOYJHW-UHFFFAOYSA-M
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):
    0.64
  • 重原子数:
    18
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    40.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

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文献信息

  • 1,4,2-Diazaphospholidine-3,5-diones and Related Compounds: A Lecture on Unpredictability in Catalysis
    作者:Frank U. Richter
    DOI:10.1002/chem.200900039
    日期:2009.5.18
    Whereas 1‐organyl‐phospholanes and 1‐organyl‐2,3‐dihydro‐1H‐phospholes catalyze isocyanate oligomerization, the reaction of isocyanates with 1‐organyl‐2,5‐dihydro‐1H‐phospholes results in the formation of 1,3‐dienes and a novel class of P‐heterocycles, 1,4,2‐diazaphospholidine‐3,5‐diones. Isothiocyanates and carbodiimides exhibit analogous behavior. The resultant species readily form P‐oxides, P‐sulfides
    1-有机基-膦基化合物和1-有机基-2,3-二氢-1H-基团催化异氰酸酯的低聚反应,异氰酸酯与1-有机基-2,5-二氢-1H-基团的反应导致形成1 ,3-二烯和一类新颖的P-杂环,1,4,2-二氮吡啶-3,5-二酮。异硫氰酸酯和碳二亚胺表现出相似的行为。由此产生的物种很容易形成P-氧化物,P-硫化物(见图)和季鎓盐。
  • 1,4,2-diazaphospholidine derivatives
    申请人:Richter Frank
    公开号:US08729304B2
    公开(公告)日:2014-05-20
    The present invention relates to a 1,4,2-diazaphospholidine of the formula (1) wherein R1, R2 represent, independently of one another, saturated or mono- or polyunsaturated C1-C20-alkyl, -alkenyl, -alkynyl or C5-C40-aryl groups optionally substituted or interrupted by at least one heteroatom selected from the group consisting of N, O, S, and halogen, and X represents identical or different substituents selected from the group consisting of O, S, and N—R2.
    本发明涉及一种化学式为(1)的1,4,2-二氮环丙烷,其中R1,R2分别表示饱和或单烯烃、多烯烃C1-C20烷基、烯基、炔基或C5-C40芳基,可选地被至少一个来自N、O、S和卤素的杂原子取代或中断,而X代表从O、S和N—R2的群中选择的相同或不同的取代基。
  • 1 4,2-DIAZAPHOSPHOLIDINE DERIVATIVES
    申请人:Bayer MaterialScience AG
    公开号:US20140221650A1
    公开(公告)日:2014-08-07
    The present invention relates to novel 1,4,2-diazaphospholidine derivatives, to a process for preparation thereof and to use as catalysts.
    本发明涉及一种新型的1,4,2-二氮杂环丙烷生物,其制备方法及用作催化剂的用途。
  • 1,4,2-DIAZAPHOSPHOLIDIN-DERIVATE
    申请人:Bayer Intellectual Property GmbH
    公开号:EP2344510B1
    公开(公告)日:2013-06-19
  • US8729304B2
    申请人:——
    公开号:US8729304B2
    公开(公告)日:2014-05-20
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同类化合物

磷杂环戊-3-烯 9-磷杂二环[3.3.1]壬烷 4,8-二甲基-2-磷酸双环[3.3.1]壬烷 3,3-二甲基-1,2-二叔-丁基-二磷杂环丙烷 2-氧杂环烷酮,均聚物,氧代二-2,1-乙二基酯 1,3,4-三甲基-delta(3)-磷杂环戊烯-1,1-二氯化物 1,1,3,3-四(二甲基氨基)-1,3-二磷杂环丁二烯 1-Chlor-3,4-dimethyl-2(3)-phospholen {NiBr2-1.2-Bis-dimethylphosphino-aethan}Br cyclohex-1-enylphosphonic difluoride trans-2-Ethyl-phosphiran β-[PNtBu]4 (Z)-Cyclooctene; compound with bromine bis{1,2-bis(dimethylphosphino)ethane}di-iodoiron 2,4-di-tert.-butyl-1,1-dimethyl-1-stanna-2,5-cyclohexadiene [Pt(hydride)(1,2-bis(diethylphosphino)ethane)2](hexafluorophosphate) 2,3,4,5,6,7-hexamethyl-9,10,11,12-tetrakis(trifluoromethyl)-1,8-diphosphatetracyclo<6.2.2.02,7.03,6>dodeca-4,9,11-triene bis(triethylphosphine)-2,4,4-trimethylplatinacyclopentane Zr[TeSi(SiMe3)3]2(Te)(1,2-bis(dimethylphosphino)ethane)2 2,3-bis-trifluoromethyl-1-phospha-bicyclo[2.2.2]octa-2,5,7-triene 5-methoxy-2,2,3,3,7-pentamethyl-1,4,6-trioxa-5λ5-phospha-spiro[4.4]non-7-ene 3,4-Bis(2,2,3,3,4,4,5,5-decafluorpentyl)-1,2-dithiet 1,2,3,4,5-Pentamethyl-phosphole 1-oxide [n-BuB(CH2P-i-Pr2)3Ag(triethylphosphine)] 1-tert-butyl-3-phospholene brominanium 2,6,10,14-Tetramethyl-1,3,9,11-tetraoxa-2,6,10,14-tetraphospha-cyclohexadecane 2,6,10,14-tetrasulfide bis(triethylphosphine)-3,3-dimethylplatinacyclobutane 1,4,9,12-tetramethyl-1,4,9,12-tetraphosphacyclohexadeca-6,4-diene 1,4,9,12-tetraoxyde 1-methyl-octahydro-1-phospha-2,3-cyclo-dicyclopropa[a,cd]pentalene 1-oxide cis-2,6-dimethyl-1,3-dioxa-2,6-diphosphacyclo-octane 2,6-disulphide N-butyl-N-(3,4-dimethyl-1-oxo-2,5-dihydro-1lambda5-phosphol-1-yl)-3,4-dimethyl-1-oxo-2,5-dihydro-1lambda5-phosphol-1-amine oxolane;triiodovanadium trans-2,6-dimethyl-1,3-dioxa-2,6-diphosphacyclo-octane 2,6-disulphide 2,6-Dimethyl-[1,2,6]oxadiphosphinane 2,6-dioxide 1-cyclohexyl-phospholane 1-sulfide 1,4-Dicyclohexyl-2,2,3,3,5,5,6,6-octamethyl-[1,4,2,3,5,6]diazatetrasilinane 1-Chloro-2-methyl-phosphole 1-oxide 1-Isopropenyltellanyl-butane 2-Dimethylphosphanylethyl(dimethyl)phosphane;tetraiodohafnium 2,7-Dimethyl-[1,2,7]oxadiphosphepane 2,7-dioxide 9-methyl-(1rP,2cH,5cH,6cP)-9-phospha-tricyclo[4.2.1.02,5]nonane 9ξ-oxide bismethano-nickelacyclotridecahexaene ethylthiolato(methyl)(1,2-bis(diisopropylphosphino)ethane)platinum(II) 1-Chloro-2-methyl-phosphole 1-sulfide