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1H-七氟丙烷 | 2252-84-8

1H-七氟丙烷结构式图片|2252-84-8结构式图片
1H-七氟丙烷
Propane,1,1,1,2,2,3,3-heptafluoro-
2252-84-8
C3HF7
170.02900
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:1H-七氟丙烷结构式
62442
名称和标识符
MDL MFCD00236614
InChIKey UKACHOXRXFQJFN-UHFFFAOYSA-N
Inchi InChI=1S/C3HF7/c4-1(5)2(6,7)3(8,9)10/h1H
SMILES FC(C(C(F)(F)F)(F)F)F
别名信息
- 中文别名 -
  • 1H-七氟丙烷
- 英文别名 -
  • Propane,1,1,1,2,2,3,3-heptafluoro-
  • 1H-HEPTAFLUOROPROPANE
  • 1,1,1,2,2,3,3-heptafluoro-propane
  • 1,1,2,2,3,3,3-heptafluoro-n-propane
  • 1H-perfluoropropane
  • 1-Hydroheptafluoropropane
  • C2F5CF2H
  • FC-227CA
  • Freon227ca
  • heptafluoropropane
  • HFC-227ca
  • UN3296
  • MFCD00236614
  • C3F7H
  • Heptafluoropropane
  • Heptafluoropropane or Refrigerant gas R 227
  • A816245
  • 1,1,1,2,2,3,3-heptafluoropropane
  • Propane, 1,1,1,2,2,3,3-heptafluoro-
  • AKOS006229170
  • SCHEMBL9651
  • NS00018854
  • Heptafluoropropane or Refrigerant gas R 227 [UN3296] [Nonfammable gas]
  • CHEBI:188748
  • 1,1,1,2,2,3,3-heptaluoropropane
  • FT-0607893
  • 33660-75-2
  • 2252-84-8
  • DTXSID4075297
物化性质
实验特性
LogP 2.44910
PSA 0.00000
折射率 1.2747 (estimate)
沸点 -16,3°C
熔点 -126.8°C (estimate)
闪点 °C
密度 1.4710 (estimate)
计算特性
精确分子量 169.99700
氢键供体数量 0
氢键受体数量 7
可旋转化学键数量 1
同位素质量 169.996647
重原子数量 10
复杂度 111
同位素原子数量 0
确定原子立构中心数量 0
不确定原子立构中心数量 0
确定化学键立构中心数量 0
不确定化学键立构中心数量 0
共价键单元数量 1
疏水参数计算参考值(XlogP) 2.9
拓扑分子极性表面积 0
安全信息
海关数据
海关编码 2903399090
海关数据

中国海关编码:

2903399090

概述:

2903399090. 其他无环烃的氟化、溴化或碘化衍生物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:5.5%. 普通关税:30.0%

申报要素:

品名, 成分含量, 用途

Summary:

2903399090. brominated,fluorinated or iodinated derivatives of acyclic hydrocarbons. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

相关文献
  • 1. Microwave spectroscopy and structures of two conformers of 1H-heptafluoropropane
    Joseph A. Fournier,Robert K. Bohn Dalton Trans. 2010 39 4575
  • 2. 856. The direct synthesis and stability of perfluoro-n-propyl-lithium
    J. A. Beel,H. C. Clark,D. Whyman J. Chem. Soc. 1962 4423
  • 3. Carbene chemistry. Part II. Migration in fluoroalkylcarbenes
    J. H. Atherton,R. Fields,R. N. Haszeldine J. Chem. Soc. C 1971 366
  • 4. 658. Perfluoroalkyl grignard reagents. Part I. The preparation and some reactions of heptafluoro-n-propylmagnesium iodide
    R. N. Haszeldine J. Chem. Soc. 1952 3423
  • 5. Organophosphorus chemistry. Part IX. Reaction of dimethyl- and bis(trifluoromethyl)-phosphines with olefins
    R. Fields,R. N. Haszeldine,J. Kirman J. Chem. Soc. C 1970 197
  • 6. Perfluoroalkyl derivatives of sulphur. Part XII. The reaction of heptafluoro-1-iodopropane with ethyl methyl sulphide, methyl trifluoromethyl sulphide, and methanethiol
    R. N. Haszeldine,R. B. Rigby,A. E. Tipping J. Chem. Soc. Perkin Trans. 1 1972 1506
  • 7. More reliable partial atomic charges when using diffuse basis sets
    Jason D. Thompson,James D. Xidos,Timothy M. Sonbuchner,Christopher J. Cramer,Donald G. Truhlar PhysChemComm 2002 5 117
  • 8. Perfluoroalkyl derivatives of sulphur. Part XI. The reaction of polyfluoromonoiodoalkanes with dimethyl disulphide
    R. N. Haszeldine,R. B. Rigby,A. E. Tipping J. Chem. Soc. Perkin Trans. 1 1972 159
  • 9. Perfluoroalkyl derivatives of sulphur. Part XVIII. Reactions of polyfluoroiodoalkanes with sodium methanethiolate in the presence of dimethyl disulphide, and related reactions
    Barry Haley,Robert N. Haszeldine,Barry Hewitson,Anthony E. Tipping J. Chem. Soc. Perkin Trans. 1 1976 525
  • 10. Perfluoroalkyl derivatives of sulphur. Part XV. Preparation and certain reactions of methyl polyfluoroalkyl sulphoxides and sulphones and their conversion into polyfluoroalkanesulphonic acids
    Robert N. Haszeldine,Rhymer B. Rigby,Anthony E. Tipping J. Chem. Soc. Perkin Trans. 1 1973 676
专业数据库参考
PubChemId 62442
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