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N,N-二乙基-4-甲基-1,3,2-二氧杂磷杂环戊烷-2-胺 | 3440-92-4

中文名称
N,N-二乙基-4-甲基-1,3,2-二氧杂磷杂环戊烷-2-胺
中文别名
——
英文名称
2-(diethylamino)-4-methyl-1,3,2-dioxaphospholane
英文别名
2-Diethylamino-4-methyl-1,3,2-dioxaphospholane;propylene diethylphosphoramidite;diethyl-(4-methyl-[1,3,2]dioxaphospholan-2-yl)-amine;2-diethylamino-4-methyl-[1,3,2]dioxaphospholane;N,N-Diaethyl-amidophosphorigsaeure-methylaethandiylester;Phosphorigsaeure-diaethylamid-methylaethandiylester;N,N-Diethyl-4-methyl-1,3,2-dioxaphospholan-2-amine
N,N-二乙基-4-甲基-1,3,2-二氧杂磷杂环戊烷-2-胺化学式
CAS
3440-92-4
化学式
C7H16NO2P
mdl
——
分子量
177.183
InChiKey
FNCVXAXAHOPRKH-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):
    1.2
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    21.7
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2934999090

SDS

SDS:8fdf0d1ac60f996b58eb26cd7bac2768
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

点击查看最新优质反应信息

文献信息

  • Imide-Amide Rearrangement of Cyclic Phosphorimidates: A Mechanistic Study
    作者:Eurico J. Cabrita、Carlos A. M. Afonso、António Gil de Oliveira Santos
    DOI:10.1002/1521-3765(20010401)7:7<1455::aid-chem1455>3.0.co;2-u
    日期:2001.4.1
    imide -amide rearrangement of cyclic phosphorimidates. As a result of this work new types of oligomeric organophosphorus compounds, formed by a novel 1,4-addition type ring opening polymerisation, were identified. These compounds are the stable intermediates of the imide-amide rearrangement, which upon heating yield the previously reported rearranged product. A detailed study of the mechanism of the Lewis
    旨在开发适用于不对称化学的手性环状草酰氮和二氮杂酰胺的制备的新合成途径的研究使我们对环状亚磷酸酯的酰亚胺-酰胺重排进行了研究。作为这项工作的结果,鉴定了通过新型的1,4-加成型开环聚合反应形成的新型低聚有机化合物。这些化合物是酰亚胺-酰胺重排的稳定中间体,加热时可得到先前报道的重排产物。报道了对路易斯酸催化的酰亚胺-酰胺重排机理和最终产物的立体化学控制的详细研究。结果,阐明了完整的机理,并提出了在重新排列的碳原子处保留构型的证据。
  • Process for the preparation of phosphorus derivatives of secondary
    申请人:Novo Industri A/S
    公开号:US04082745A1
    公开(公告)日:1978-04-04
    An improvement in the conversion of penam and cephem compounds to secondary ammonium salts of phosphite amides thereof by reacting as follows: ##STR1## wherein --R, is the non-reacting balance of the penam or cephem compound and ##STR2## ARE NON-REACTING SUBSTITUENTS. Catalytic amounts of H--N< or the hydrogenhalide thereof may be present in the reaction medium.
    通过以下反应改进将青霉素头孢菌素化合物转化为磷酸酯酰胺的二级盐:其中--R是青霉素头孢菌素化合物的非反应平衡部分,##STR2## 是非反应的取代基。在反应介质中可能存在催化量的H--N<或其氢卤化物。
  • Cyclic Phosphites of Some Aliphatic Glycols
    作者:H. J. Lucas、F. W. Mitchell、C. N. Scully
    DOI:10.1021/ja01168a032
    日期:1950.12
  • Gilyarov, V. A.; Tikhonina, N, A.; Shcherbina, T. M., Journal of general chemistry of the USSR, 1980, vol. 50, # 7, p. 1157 - 1161
    作者:Gilyarov, V. A.、Tikhonina, N, A.、Shcherbina, T. M.、Kabachnik, M. I.
    DOI:——
    日期:——
  • Krutskii,L.N. et al., Journal of general chemistry of the USSR, 1976, vol. 46, p. 505 - 517
    作者:Krutskii,L.N. et al.
    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-Dipropylamino-<1,3,2 λ3>dioxaphospholan 2-ethoxy-[1,3,2]oxazaphospholidine Ethylen-2.2.2-trifluorethylphosphit-ozonid 2-dimethylamino-(3ar,9ac,3'ar',9'ac')-hexadecahydro-2λ5-[2,2']spirobi(cycloocta[1,3,2]dioxaphosphole) 2,7-dimethyl-1,4,6,9-tetraoxa-5(λ5)-phosphaspiro<4.4>nonane Aethylenselenit 4,5-bis-trifluoromethyl-2λ5-spiro[[1,3,2]dioxaphosphole-2,1'-(2,8,9-trioxa-1-phospha-adamantane)] 5,5-Difluoro-1,4,6,9-tetraoxa-5λ6-tellura-spiro[4.4]nonane N-methyl-1-(1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-5-yl)-N-(1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-5-ylmethyl)methanamine 2-methyl-5-(2,2,2-trichloroethoxy)-1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-3-one Butan-2,3-diylselenit (4r,5t-dimethyl-[1,3,2]dioxaphospholan-2-yl)-dimethyl-amine 3,3-dibromo-2-fluoro-4-propyl-1,2λ5-oxaphosphetane 2-Fluor-2,2-dibrom-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan [1,3,2]dioxaphospholan-2-yl-ethyl-amine 2-tert-butylamino-2,2-difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 3,3-dichloro-2-fluoro-4-propyl-1,2λ5-oxaphosphetane 1,1-Dibromo-3,5,8-tris-(1,1,2,2-tetrafluoro-ethyl)-2,6,7-trioxa-1λ5,4-diphospha-bicyclo[2.2.2]octane 2-Brom-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan dibutyl-(4-methyl-[1,3,2]dioxaphospholan-2-yl)-amine 2-(tert-butylimino)-1,3,2,4-oxaazaphosphaboretidine 1,1,3,3,5,5,7,7-Tetrakis--tetraphosphazatetraen 2-Chlor-2,2-dibrom-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan 2-Propoxy-[1,3,2]dioxaphospholan-4-one 2-Fluor-2,2-dichlor-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan 2-fluoro-3-methyl-[1,3,2]oxazaphospholidine 2,2,2,4-tetrachloro-3-isopropyl-4-triflyoromethyl-1,3,2-λ5-oxazaphosphetane 1,1-Dichloro-3,5,8-tris-(1,1,2,2-tetrafluoro-ethyl)-2,6,7-trioxa-1λ5,4-diphospha-bicyclo[2.2.2]octane 2-ethoxy-2-fluoro-2λ5-[1,3,2]dioxaphospholan-2-yl phosphoric acid-(2-ethyl-2-butyl-propanediyl ester)-(2-bromo-propyl ester) (4,4-dimethyl-1,3,2-dioxaphospholan-2-yl) 2,2,2-trifluoroacetate 2-Dimethylamino-4,4,5,5-tetrakis(trifluormethyl)-1,3,2λ3-dioxaphospholan 2,3,3-Trichloro-2,2-diethyl-4-trichloromethyl-2λ5-[1,2]oxaphosphetane (5-tert-butyl-[1,3,2]dioxaphosphinan-2-yl)-dimethyl-amine 2-cyclohexyl-[1,3,2]dioxaphospholane (4-tert-Butyl-[1,3,2]dioxaphospholan-2-yl)-diethyl-amine N-Methyl-N-[1-methyl-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaphospholan-2-yloxy)-propyl]-acetamide 2,2-Dichlor-2-dimethylamino-4,4,5,5-tetrakis(trifluormethyl)-1,3,2λ5-dioxaphospholan methyl-2-trioxaphosphocanne-1,3,6,2 5-dimethylamino-2,4-diisopropylidene-1,3,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane