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2-(2-amino-5-methyl-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol is a chemical compound with the molecular formula C10H12F6NO. It is a secondary alcohol that features a hexafluoroisopropanol moiety, which is a fluorinated alcohol known for its strong hydrogen bond donating capability. 2-(2-amino-5-methyl-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol is synthesized from 2-amino-5-methylphenol and hexafluoroacetone and is characterized by its unique structure and properties that make it valuable in various chemical applications.

1992-07-0

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1992-07-0 Usage

Uses

Used in Organic Synthesis:
2-(2-amino-5-methyl-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol is used as a reagent or solvent in organic synthesis for its ability to participate in a range of chemical reactions and processes. Its strong hydrogen bond donating capability makes it a versatile component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(2-amino-5-methyl-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol is used as a building block or intermediate in the development of new drugs. Its unique chemical properties allow it to be incorporated into the molecular structures of potential therapeutic agents, enhancing their efficacy and selectivity.
Used in Agrochemical Industry:
2-(2-amino-5-methyl-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol is also utilized in the agrochemical industry, where it serves as a key component in the synthesis of pesticides and other agricultural chemicals. Its properties contribute to the development of more effective and environmentally friendly agrochemicals.
Used in Material Development:
2-(2-amino-5-methyl-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol's structure and properties make it potentially useful for developing new materials with unique characteristics. It can be incorporated into the design of advanced materials for various applications, such as high-performance polymers, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 1992-07-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1992-07:
(6*1)+(5*9)+(4*9)+(3*2)+(2*0)+(1*7)=100
100 % 10 = 0
So 1992-07-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9F6NO/c1-5-2-3-7(17)6(4-5)8(18,9(11,12)13)10(14,15)16/h2-4,18H,17H2,1H3

1992-07-0Downstream Products

1992-07-0Relevant academic research and scientific papers

Synthesis of metathesis catalysts with fluorinated unsymmetrical N,N’-diaryl imidazoline-based NHC ligands

Masoud, Salekh M.,Topchiy, Maxim A.,Peregudov, Alexander S.,Roisnel, Thierry,Dixneuf, Pierre H.,Bruneau, Christian,Osipov, Sergey N.

, p. 66 - 76 (2017)

New olefin metathesis catalysts bearing unsymmetrical fluorinated NHC ligands with hexafluoroisopropylmethoxy group in ortho-positions of N-aryl-substituent have been synthesized. The effects of mono-ortho-arylsubstitution and the replacement of para-meth

19F CEST imaging probes for metal ion detection

Peng, Qiaoli,Yuan, Yaping,Zhang, Huaibin,Bo, Shaowei,Li, Yu,Chen, Shizhen,Yang, Zhigang,Zhou, Xin,Jiang, Zhong-Xing

, p. 6441 - 6446 (2017)

For detecting metal ions with 19F chemical exchange saturation transfer magnetic resonance imaging (19F CEST MRI), a class of novel fluorinated chelators with diverse fluorine contents and chelation properties were conveniently synthesized on gram scales. Among them, a DTPA-derived chelator with high sensitivity and selectivity was identified as a novel 19F CEST imaging probe for simultaneously detecting multiple metal ions.

HYPERVALENT RADIOACTIVE ASTATINE OR IODINE COMPOUNDS, AND PREPARATION METHODS THEREOF

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Page/Page column 21-22, (2011/09/14)

The present invention relates to a compound having formula (I): wherein: - X is in particular 125I Or 211At; - R1 and R'1 are independently from each other chosen preferably from the group consisting of electron

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