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Merck
CN

567191

Sigma-Aldrich

2,2,3,3-四氟-1,4-丁二醇

别名:

2,2,3,3-Tetrafluorobutanediol, NSC 95113, Tetrafluoro-1,4-butanediol

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About This Item

线性分子式:
HOCH2CF2CF2CH2OH
CAS号:
分子量:
162.08
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

表单

solid

质量水平

沸点

110-112 °C/13 mmHg (lit.)

mp

77-82 °C (lit.)

官能团

fluoro
hydroxyl

SMILES字符串

OCC(F)(F)C(F)(F)CO

InChI

1S/C4H6F4O2/c5-3(6,1-9)4(7,8)2-10/h9-10H,1-2H2

InChI key

CDZXJJOGDCLNKX-UHFFFAOYSA-N

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应用

2,2,3,3-Tetrafluoro-1,4-butanediol may be used in the synthesis of the following:
  • segmented polyurethanes(SPU 001-002)
  • PFPE(perfluoro-polyether)modified segmented polyurethanes (SPU 003-006)
  • 2,2,3,3-tetrafluorobutane-1,4-diyl dicarbamate
  • 2,2,3,3-tetrafluorobutane-1,4-diyl dinitrate
  • 2,2,3,3-tetrafluoro-4-((trimethylsilyl)methoxy)butanol
Reactant for:
Enzymic synthesis of silicone fluorinated aliphatic polyester amides

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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"Synthesis of nitrate ester and nitramine derivatives of polyfluoro alkyl compounds for high energy materials"
Srinivas D and Ghule.DV
Royal Society of Chemistry Advances, 6(10), 7712-7716 (2016)
"Comparison of Photocyclization Reactions of Fluoro-vs Nonfluoro-Substituted Polymethyleneoxy Donor Linked Phthalimides"
Park JH, et al.
Bulletin of the Korean Chemical Society,, 34(4), 1108-1114 (2013)
"Synthesis and surface properties of environmentally responsive segmented polyurethanes"
Vaidya A and Chaudhury.KM
Journal of Colloid and Interface Science, 249(1), 235-245 (2002)
Piotr Król et al.
Colloid and polymer science, 290(10), 879-893 (2012-06-19)
The polarity of polyurethane coats was studied on the basis of the goniometric method for determination of wetting angle values, on the basis of calculated surface free energy (SFE) values by the van Oss-Good and Owens-Wendt methods, and on the
Piotr Król et al.
Colloid and polymer science, 289(15-16), 1757-1767 (2011-12-02)
WAXS, DSC and AFM methods were employed to compare phase structures of the coatings obtained from waterborne polyurethane cationomers which had been synthesised in the reaction of some diisocyanates (MDI, IPDI, TDI and HDI) with polyoxyethylene glycols (M = 600 and 2,000)

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