34454-97-2 Usage
Description
1,1,2,2,3,3,4,4,4-nonafluoro-N-(2-hydroxyethyl)-N-methylbutane-1-sulphonamide is a perfluorinated compound (PFC) derived from Nonafluoro-1-butanesulfonyl Fluoride (N649320). It is characterized by its unique chemical structure, which includes a perfluorinated butane backbone with a sulphonylamide functional group. 1,1,2,2,3,3,4,4,4-nonafluoro-N-(2-hydroxyethyl)-N-methylbutane-1-sulphonamide is known for its specific properties, such as high chemical and thermal stability, and is utilized in various applications due to these characteristics.
Uses
Used in Organic Synthesis:
1,1,2,2,3,3,4,4,4-nonafluoro-N-(2-hydroxyethyl)-N-methylbutane-1-sulphonamide is used as a building block in organic synthesis for the creation of various perfluorinated compounds. Its unique structure and properties make it a valuable component in the synthesis of complex molecules with specific characteristics, such as enhanced solubility, stability, and reactivity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,1,2,2,3,3,4,4,4-nonafluoro-N-(2-hydroxyethyl)-N-methylbutane-1-sulphonamide is used as an intermediate in the development of drugs with improved pharmacokinetic and pharmacodynamic properties. The perfluorinated nature of the compound can enhance the drug's solubility, stability, and bioavailability, leading to more effective therapeutic outcomes.
Used in Material Science:
1,1,2,2,3,3,4,4,4-nonafluoro-N-(2-hydroxyethyl)-N-methylbutane-1-sulphonamide is also utilized in material science for the development of advanced materials with specific properties. Its high chemical and thermal stability make it suitable for applications in various industries, such as aerospace, electronics, and automotive, where materials with exceptional performance are required.
Used in Environmental Applications:
Due to its unique properties, 1,1,2,2,3,3,4,4,4-nonafluoro-N-(2-hydroxyethyl)-N-methylbutane-1-sulphonamide can be employed in environmental applications, such as the treatment of contaminated water or soil. Its high chemical stability and reactivity can help in the removal or degradation of harmful pollutants, contributing to a cleaner and safer environment.
Check Digit Verification of cas no
The CAS Registry Mumber 34454-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,5 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34454-97:
(7*3)+(6*4)+(5*4)+(4*5)+(3*4)+(2*9)+(1*7)=122
122 % 10 = 2
So 34454-97-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8F9NO3S/c1-17(2-3-18)21(19,20)7(15,16)5(10,11)4(8,9)6(12,13)14/h18H,2-3H2,1H3
34454-97-2Relevant articles and documents
A kind of acrylic acid (N - methyl perfluoroalkyl sulfuryl amidogen) ethyl ester preparation method
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Paragraph 0027; 0030; 0032; 0035, (2019/07/04)
The invention relates to an acrylic acid (N - methyl perfluoroalkyl sulfuryl amidogen) ethyl ester preparation method, comprising the following steps: S1. In order to perfluoroalkyl-fluoride and methylamine as raw materials, inorganic salt aqueous solution as the solvent, remain below the 4 °C temperature of reaction, shall be N - methyl perfluoroalkyl sulfonamide; S2. Under the action of the alkaline catalyst, S1 of the prepared N - methyl perfluoroalkyl sulfonamide with vinyl carbonate reaction, shall be N - hydroxyethyl - N - methyl perfluoroalkyl sulfonamide; S3. In the presence of hydroquinone, S2 prepared N - hydroxyethyl - N - methyl perfluoroalkyl sulfonamide with acrylic acid methyl ester exchange reaction, be acrylic acid (N - methyl perfluoroalkyl sulfuryl amidogen) acetic ester. The advantage is: in order to salt water solution is used as the preparation N - methyl perfluoroalkyl sulfonamide solvent, overcome in the prior art that use only the bias of the non-aqueous solvent, in the final waste water content greatly reduced COD, environment-friendly; yield and high purity.