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1,2-oxaphospholane | 6920-93-0

中文名称
——
中文别名
——
英文名称
1,2-oxaphospholane
英文别名
oxaphospholane
1,2-oxaphospholane化学式
CAS
6920-93-0
化学式
C3H7OP
mdl
——
分子量
90.0617
InChiKey
FXPDGSSSQUFIPW-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):
    0.1
  • 重原子数:
    5
  • 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:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    4-甲基-3戊烯-2-酮 、 Phosphorous acid, bis(1-methylethyl) ester 、 溶剂黄1461,2-oxaphospholane Sodium sulfate-III 作用下, 反应 0.42h, 以yielded 27.5 g of a first fraction with a boiling point of 68°-75° C./10 mm Hg的产率得到2-oxo-2-isopropoxy-3,3,5-trimethyl-5-diisopropylphosphono-1,2-oxaphospholane
    参考文献:
    名称:
    1,2-Oxaphospholanes
    摘要:
    式为##STR1##的2-氧代-2-烷氧基-5-二烷基膦酸酯-1,2-氧杂膦环可以由α,β-不饱和酮和2个或更多个二烷基膦酸酯制备。显然,γ-酮膦酸酯是该反应的中间体,因为这些化合物与1个或更多个二烷基膦酸酯反应也能产生氧杂膦环。两种反应都由碱性催化剂促进。新的氧杂膦环衍生物在热分解方面相当稳定。它们可以用作环氧树脂的阻燃剂。
    公开号:
    US04042649A1
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文献信息

  • 1,2-Oxaphospholanes
    申请人:Ciba-Geigy Corporation
    公开号:US04042649A1
    公开(公告)日:1977-08-16
    2-Oxo-2-alkoxy-5-dialkylphosphono-1,2-oxaphospholanes of the formula ##STR1## in which R.sub.1 to R.sub.7 are hydrocarbon radicals can be prepared from .alpha.,.beta.-unsaturated ketones and 2 or more moles of a dialkyl phosphite. Obviously .gamma.-ketophosphonates are intermediates of this reaction as these compounds react with 1 or more moles of dialkyl phosphite in yielding the oxaphospholanes too. Both reactions are promoted by alkaline catalysts. The new oxaphospholane derivatives are considerably stable against thermal decomposition. They can be used as flame retardants in epoxy resins.
    式为##STR1##的2-氧代-2-烷氧基-5-二烷基膦酸酯-1,2-氧杂膦环可以由α,β-不饱和酮和2个或更多个二烷基膦酸酯制备。显然,γ-酮膦酸酯是该反应的中间体,因为这些化合物与1个或更多个二烷基膦酸酯反应也能产生氧杂膦环。两种反应都由碱性催化剂促进。新的氧杂膦环衍生物在热分解方面相当稳定。它们可以用作环氧树脂的阻燃剂。
  • Epoxy resins flameproofed with 1,2-oxaphospholanes
    申请人:Ciba-Geigy Corporation
    公开号:US04105630A1
    公开(公告)日:1978-08-08
    2-Oxo-2-alkoxy-5-dialkylphosphono-1,2-oxaphos-pholanes of the formula ##STR1## in which R.sub.1 to R.sub.7 are hydrocarbon radicals can be prepared from .alpha., .beta.-unsaturated ketones and 2 or more moles of a dialkyl phosphite. Obviously .beta.-ketophosphonates are intermediates of this reaction as these compounds react with 1 or more moles of dialkyl phosphite in yielding the oxaphospholanes too. Both reactions are promoted by alkaline catalysts. The new oxaphospholane derivatives are considerably stable against thermal decomposition. They can be used as flame retardants in epoxy resins.
    式为##STR1##的2-氧代-2-烷氧基-5-二烷基膦酸酯-1,2-氧杂膦烷可以由α,β-不饱和酮和2个或更多摩尔的二烷基膦酸酯制备。显然,β-酮膦酸酯是该反应的中间体,因为这些化合物与1个或多个摩尔的二烷基膦酸酯反应,也会生成氧杂膦烷。这两种反应都由碱性催化剂促进。新的氧杂膦烷衍生物相对于热分解来说相当稳定。它们可以用作环氧树脂的阻燃剂。
  • Polymers flameproofed with 1,2-oxaphospholanes
    申请人:Ciba-Geigy Corporation
    公开号:US04113669A1
    公开(公告)日:1978-09-12
    2-Oxo-2-alkoxy-5-dialkylphosphono-1,2-oxaphospholanes of the formula ##STR1## in which R.sub.1 to R.sub.7 are hydrocarbon radicals can be prepared from .alpha.,.beta.-unsaturated ketones and 2 or more moles of a dialkyl phosphite. Obviously .gamma.-ketophosphonates are intermediates of this reaction, as these compounds react with 1 or more moles of dialkyl phosphite in yielding the oxaphospholanes too. Both reactions are promoted by alkaline catalysts. The new oxaphospholane derivatives are considerably stable against thermal decomposition. They are compatible with polymeric materials and can be used as flame protecting agent for plastics and resins, for example, in polyurethane foams.
    式子为##STR1##的2-氧代-2-烷氧基-5-二烷基膦酸酯-1,2-氧代膦环己烷可以通过α,β-不饱和酮和2个或更多摩尔的二烷基膦酸酯制备。显然,γ-酮膦酸酯是这种反应的中间体,因为这些化合物与1个或更多摩尔的二烷基膦酸酯反应也能产生氧代膦环己烷。这两种反应都受碱性催化剂的促进。新的氧代膦环己烷衍生物在热分解方面相当稳定。它们与聚合材料相容,并可用作塑料和树脂的阻燃剂,例如在聚氨酯泡沫中。
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同类化合物

2-甲基-1,2-噁膦-5-酮 2-氧化物 3-methyl-3-trimethylsilyloxy-2-trimethylsilylamino-2-trimethylsilylimino-[1,2]-oxaphospholane 3-methyl-3-trimethylsilyloxy-2-trimethylsilylmethyl-2-trimethylsilylimino-[1,2]-oxaphospholane 3,5,5-trimethyl-3-trimethylsilyloxy-2-trimethylsilylamino-2-trimethylsilylimino-[1,2]-oxaphospholane cis-2,3,5,5-Tetramethyl-1,2-oxaphospholan-3-ol 2-oxide 2-ethyl-3,5,5-trimethyl-2-oxo-2λ5-[1,2]oxaphospholan-3-ol 2,4-Dimethyl-2-oxo-1,2-oxaphospholan 2-ethyl-5-methyl-[1,2]oxaphospholane 2-sulfide 2-Aethyl-2-oxo-1-oxa-2-phospholan 1-hydroxy-3,6,7,7,8-pentamethyl-8-oxo-8-phospha-9-oxabicyclo<4.3.0>nonane 1,2-Oxaphospholan-3-ol, 2-(ethylthio)-3,5,5-trimethyl-, 2-oxide, cis- 2,2,2-trimethyl-2λ5-[1,2]oxaphospholane 2,2,2-triethyl-2λ5-[1,2]oxaphospholane methyl 3-hydroxyl-4-terta-butyldimethylsilylbutane-1,3-cyclic thiophosphonate 2-ethyl-1,2-oxaphospholan-5-one 2-oxide 2-Methyl-2-oxo-1,2-oxaphospholan 5-Methyl-1-oxa-5λ5-phosphaspiro <4,5>-decan 5-Methyl-1-oxa-5λ5-phosphaspiro<4,4>-nonan 5-dimethylamino-7-isopropylidene-4,8,8-trimethyl-1,6-dioxa-4-aza-5λ5-phospha-spiro[4.4]nonan-9-one 2-chloromethyl-2-oxo-2λ5-[1,2]oxaphospholan-5-one 2,4-dimethyl-2-oxo-2λ5-[1,2]oxaphospholan-5-one 2-isopropylidene-3,3,3-trimethoxy-4,4-dimethyl-3λ5-[1,3]oxaphospholan-5-one 2-Oxo-1,2-oxaphospholan-2-ium 2-ethoxy-3,5,5-trimethyl-2-thioxo-2λ5-[1,2]oxaphospholan-3-ol 2,3,5,5-tetramethyl-3-chlor-1,2-oxaphospholan-2-oxide 2-tert-Butyl-3-chlor-5-methyl-1,3-oxaphospholan 1,2-oxaphospholane (3S)-2-(diethylamino)-2-hydroxy-2,3,5,5-tetramethyl-1,2lambda5-oxaphospholan-3-ol (3R)-2-(diethylamino)-2-hydroxy-2,3,5,5-tetramethyl-1,2lambda5-oxaphospholan-3-ol (2S)-2-methyl-2-oxo-1,2lambda5-oxaphospholan-5-one (2R)-2-methyl-2-oxo-1,2lambda5-oxaphospholan-5-one 2,2-bis(but-3-enoxy)-2-ethoxy-3-methyl-1,2λ5-oxaphospholane 2,2-bis(but-3-enoxy)-2,3-dimethyl-1,2λ5-oxaphospholane (5R)-5-[(1S)-1,2-dihydroxyethyl]-2-hydroxy-3-oxo-1,3-oxaphospholan-3-ium-4-one 3-(1,3-Oxaphospholan-2-yl)prop-2-enenitrile (3S)-2-ethylsulfanyl-3,5,5-trimethyl-2-oxo-1,2lambda5-oxaphospholan-3-ol 2-(Diethylamino)-3,5,5-trimethyl-2-sulfanylidene-1,2lambda5-oxaphospholan-3-ol 2-Ethyloxaphospholan-5-one (4R)-3-methyl-4-(3-methyl-1,3-oxaphospholan-4-yl)-1,3-oxaphospholane (3S)-2,3,5,5-tetramethyl-2-oxo-1,2lambda5-oxaphospholan-3-ol Diethyl-(2-thioxo-[1,2]oxaphospholan-2-yl)-amine methyl 3,4-dihydroxyl-butane-1,3-cyclic thiophosphonate 2-chloro-2-thiono-5-methyl-1,2-oxaphospholane 2-thio-2-dimethylamino-5-methyl-1,2-oxaphospholane