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2-氯-4-甲基-1,3,2-二氧杂磷杂环戊烷 | 6362-86-3

中文名称
2-氯-4-甲基-1,3,2-二氧杂磷杂环戊烷
中文别名
——
英文名称
2-chloro-4-methyl-dioxaphospholane
英文别名
2-Chloro-4-methyl-1,3,2-dioxaphospholan;2-chloro-4-methyl-1,3,2-dioxaphospholane
2-氯-4-甲基-1,3,2-二氧杂磷杂环戊烷化学式
CAS
6362-86-3
化学式
C3H6ClO2P
mdl
——
分子量
140.506
InChiKey
CJOGVHAUJHBLPB-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:
    46.5-48 °C(Press: 13 Torr)

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    7
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2934999090

SDS

SDS:14f141ba8481eaf33c5b8b954687004d
查看

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Modro,T.; Sokolowski,J., Roczniki Chemii, 1966, vol. 40, p. 1203 - 1206
    摘要:
    DOI:
  • 作为产物:
    描述:
    1,2-丙二醇三氯化磷 作用下, 以 二氯甲烷 为溶剂, 以90.3 %的产率得到2-氯-4-甲基-1,3,2-二氧杂磷杂环戊烷
    参考文献:
    名称:
    三氟代环状磷酸酯类化合物及其制备方法和应用
    摘要:
    本发明涉及一种三氟代环状磷酸酯类化合物及其制备方法和应用。三氟代环状磷酸酯类化合物具有如下结构通式: 所述制备方法包括以下反应步骤:(1)将式II所示的二醇化合物与三氯化磷进行环合反应得到式III所示化合物;(2)将步骤(1)得到的式III化合物经过卤化反应得到式IV所示化合物;(3)将步骤(2)得到的式IV所示化合物与含氟化试剂发生氟卤交换反应,制备得到式I所示化合物。所述三氟代环状磷酸酯类化合物可用作一种新型的锂电池电解液添加剂。
    公开号:
    CN116063352A
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文献信息

  • N-Phosphorylated lactams
    作者:A. B. Ouryupin、I. A. Rakhov、V. A. Kolesova、P. V. Petrovskii、T. A. Mastryukova、M. I. Kabachnik
    DOI:10.1007/bf00696723
    日期:1995.11
    The phosphorylation ofN-trimethylsilyllactams by phosphorus(III) acid chlorides results in correspondingN-phosphinolactams in high yields. The derivatives thus obtained have been used in the synthesis ofN-phosphoryl- andN-thiophosphoryllactams. The reversibility of the reaction of phosphinolactams has been established.
    N-三甲基甲硅烷基内酰胺被磷(III)酰氯磷酸化产生相应的N-膦内酰胺,收率很高。如此获得的衍生物已用于合成N-磷酰基-和N-硫代磷酰基内酰胺。膦内酰胺反应的可逆性已经确立。
  • Cyclic organophosphorus compounds as possible pesticides. Part I. 1,3,2-Dioxaphospholans
    作者:R. S. Edmundson、A. J. Lambie
    DOI:10.1039/j39660001997
    日期:——
    Butane-2,3-diol and 2,3-dimethylbutane-2,3-diol have been converted into substituted 2-mercapto-2-thiono-1,3,2-dioxaphospholans, and thence into 2-(N-substituted carbamoylmethyl)thio-derivatives. Some new ring-substituted 1,3,2-dioxaphospholans, with alkoxy, alkylthio, and dimethylamino groups attached to phosphorus, have also been prepared from aliphatic 1,2-diols. The hydrolytic stability and insecticidal
    2,3-丁二醇和2,3-二甲基-2,3-二醇已被转化为取代的2-巯基-2-硫代-1,3,2-二氧杂膦酸酯,因此被转化为2-(N-取代的氨基甲酰基甲基)硫代衍生物。还已经从脂族1,2-二醇制备了一些新的环取代的1,3,2-二氧杂膦酸酯,其具有连接到磷上的烷氧基,烷硫基和二甲基氨基。简要讨论了酯的水解稳定性和杀虫活性。
  • Cyclic organophosphorus compounds. I. Synthesis and infrared spectral studies of cyclic hydrogen phosphites and thiophosphites
    作者:A. Zwierzak
    DOI:10.1139/v67-411
    日期:1967.11.1
    A general synthetic procedure leading to cyclic hydrogen phosphites has been devised. The effect of solvent on the P==O and P—H infrared stretching modes of cyclic hydrogen phosphites and thiophosphites has been studied. It is concluded that association of cyclic hydrogen phosphites is attributable to dipole–dipole interactions rather than to hydrogen bonding.
    已经设计了导致环状亚磷酸氢酯的一般合成程序。研究了溶剂对环状亚磷酸氢酯和硫代亚磷酸酯的 P==O 和 P-H 红外伸缩模式的影响。结论是环状亚磷酸氢盐的缔合归因于偶极-偶极相互作用而不是氢键。
  • 7-[(5'-N-methylthioacetamido)-adipoamido] cephalosporin derivatives
    申请人:——
    公开号:US04036833A1
    公开(公告)日:1977-07-19
    New N-substituted thio (or sulfinyl) aliphatic acylcephalosporin C and their derivatives at the 3rd position have been prepared. The compounds are useful as intermediates for recovering cephalosporin C and deacetoxycephalosporin C from their fermentation broth and also for preparing 7-aminocephalosporanic acid and its derivatives at the 3rd position.
    新的N取代硫(或亚砜基)脂肪酰头孢菌素C及其在第3位的衍生物已经制备。这些化合物可用作从发酵液中回收头孢菌素C和脱乙酰氧头孢菌素C的中间体,也可用于制备第3位的7-氨基头孢菌酸及其衍生物。
  • Konovalova, I. V.; Mironov, V. F.; Ofitserov, E. N., Journal of general chemistry of the USSR, 1983, vol. 53, # 2, p. 414
    作者:Konovalova, I. V.、Mironov, V. F.、Ofitserov, E. N.、Pudovik, A. N.
    DOI:——
    日期:——
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同类化合物

尿苷5'-二磷酸酯溴乙酰醇 N,N-二乙基-4-甲基-1,3,2-二氧杂磷杂环戊烷-2-胺 4,4,5,5-四甲基-1,3,2-二氧磷杂环戊烷-2-醇 2-氯-4-甲基-1,3,2-二氧杂磷杂环戊烷 2-氯-4,4,5,5-四甲基-1,3,2-二氧磷杂环戊烷 2-氯-1,3,2-二氧磷杂环戊烷 (3,5-二甲基苯基)[羟基(吡啶-4-基甲基)-lambda~5~-氮烷基]甲酮 2-(2-ethylbutoxy)-2-oxo-1,3,2-dioxaphospholane 2-(tert-butoxycarbonylamino)ethoxy-2-oxo-1,3,2-dioxaphospholane 5-dimethylamino-7-isopropylidene-8,8-dimethyl-1,4,6-trioxa-5λ5-phospha-spiro[4.4]nonan-9-one 5-dipropylaminomethyl-1,4,6,9-tetraoxa-5-phosphaspiro<4.4>nonane ethylenedioxy-O-(4,4-dimethyl-1,3-butadien-2-yl)phosphite pentamethyl-2,3,3,4,4 dioxaphospholane-1,3,2 propargyl ethylene phosphate 2-methylthio-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2λ5-dioxaphospholane 2,2-bis(diethylamino)-2-(1,1,1,3,3,3-hexafluoro)isopropoxy-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2λ5ς5-dioxaphospholane 4,4,5,5-tetrakis(trifluoromethyl)-2-<2,2,2-trifluoro-1-(trifluoromethyl)ethoxy>-spiro-<1,3,2λ5-dioxaphospholane-2,2'-(1,3,2λ5) dioxaphosphorinane> 4-chloromethyl-[1,3,2]dioxaphospholane 2-oxide 5-Methoxy-2,2,3,3-tetramethyl-7,9-bis(trifluoromethyl)-1,4,6-trioxa-5lambda5-phosphaspiro[4.4]non-7-en-9-ol 2,2-Dimethoxy-2-methyl-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2lambda5-dioxaphospholane 5,7-Dimethyl-2,2,3,3,9,9,10,10-octakis(trifluoromethyl)-1,4,6,8,11-pentaoxa-5lambda5,7lambda5-diphosphadispiro[4.1.47.35]tetradecane Butylamino-ethylendioxyphosphin 5-Dichloromethyl-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane-2,7-dione 5-Fluoro-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane-2,7-dione Ethylendioxytributylphosphoran 2-Thiono-2-t-butyl-1,3,2-dioxaphospholan (5-TB-5-13;5'-TB-5-13)-2,2,3,3,2',2',3',3'-octamethyl-5,5'-ethane-1,2-diyldioxy-bis-(1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane) (1,4-Dioxa-6,9-dithia-5λ5-phospha-spiro[4.4]non-5-yl)-dimethyl-amine 5-Trimethylsilanylmethyl-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane-2,7-dione 5-Isopropyl-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane-2,7-dione 5-(2,2,2-Trifluoro-1-trifluoromethyl-ethoxy)-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane 2,2,2-Tris-(2,2,2-trifluoro-1-trifluoromethyl-ethoxy)-2λ5-[1,3,2]dioxaphospholane 2,2,2-trichloro-4,4-bis-chlorocarbonylmethyl-2λ5-[1,3,2]dioxaphospholan-5-one 5,6,7,12-Tetramethyl-2,2,3,3,9,9,10,10-octakis-trifluoromethyl-1,4,8,11-tetraoxa-6,12-diaza-5λ5,7λ5-diphospha-dispiro[4.1.4.1]dodecane 2,2-Difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 2-Fluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane (2-TB-5-12)-2-fluoro-4,4,5,5-tetrakis-trifluoromethyl-2,2-bis-(2,2,2-trifluoro-1-trifluoromethyl-ethoxy)-2λ5-[1,3,2]dioxaphospholane Triethoxy-ethylendioxy-phosphoran 4,4,5,5-Tetrakis(trifluormethyl)-1,3,2λ5-dioxaphospholan-2,2,2-triamin 2-fluoro-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2λ5-dioxaphospholane-2,2-diamine 2-Fluor-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan 5,7-difluoro-2,2,3,3,9,9,10,10-octakis-trifluoromethyl-6,12-bis-trimethylsilanyl-1,4,8,11-tetraoxa-6,12-diaza-5λ5,7λ5-diphospha-dispiro[4.1.4.1]dodecane [2-(1,1,1,3,3,3-hexamethyl-disilazan-2-yl)-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholan-2-ylidene]-trimethylsilanyl-amine 2,2-Di-tert-Butyl-2-chlor-4,4,5,5-tetrakis(trifluormethyl)-1,3,2λ5-dioxaphospholan 2-fluoro-2,2-dimethyl-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 2-fluoro-2,2-dimethyl-3,3,5,5-tetrakis-trifluoromethyl-2λ5-[1,4,2]dioxaphospholane 2-diethylamino-2,2-difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 2-diallylamino-2,2-difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 2-Methyl-4,4,5,5-tetrakis-trifluoromethyl-2,2-bis-(2,2,2-trifluoro-1-trifluoromethyl-ethoxy)-2λ5-[1,3,2]dioxaphospholane