55805-14-6 Usage
General Description
4-(1,1-Difluoroethyl)benzoic acid is a chemical compound that consists of a benzoic acid core with a 1,1-difluoroethyl substituent at the 4-position. It is commonly used in organic synthesis and pharmaceutical research as a building block for creating new drugs and other chemical compounds. 4-(1,1-Difluoroethyl)benzoic acid is known for its high reactivity and ability to participate in various chemical reactions, making it a valuable tool for chemists and researchers. The presence of the difluoroethyl group also gives it unique properties and potential applications in the development of new materials and chemical processes. Overall, 4-(1,1-Difluoroethyl)benzoic acid is a versatile and important chemical compound with a wide range of potential uses in the field of chemistry and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 55805-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,0 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55805-14:
(7*5)+(6*5)+(5*8)+(4*0)+(3*5)+(2*1)+(1*4)=126
126 % 10 = 6
So 55805-14-6 is a valid CAS Registry Number.
InChI:InChI=1S/C9H8F2O2/c1-9(10,11)7-4-2-6(3-5-7)8(12)13/h2-5H,1H3,(H,12,13)
55805-14-6Relevant articles and documents
Scalable Approach to Fluorinated Heterocycles with Sulfur Tetrafluoride (SF4)
Ahunovych, Volodymyr,Boretskyi, Andrii,Bugera, Maksym,Klipkov, Anton A.,Mykhailiuk, Pavel K.,Razhyk, Bohdan,Semenov, Sergey,Tarasenko, Karen,Trofymchuk, Serhii
, p. 12181 - 12198 (2021/09/13)
A general approach to fluorinated (hetero)aromatic derivatives is elaborated. The key reaction is a deoxofluorination of substituted acetophenones with sulfur tetrafluoride (SF4). In contrast to previous deoxofluorination methods, this transformation is fast, scalable (up to 70 g), and high-yielding. More than 100 novel or previously hardly accessible fluorinated heterocycles, interesting for medicinal chemistry and agrochemistry, were synthesized.
PYRROLO AND PYRAZOLOPYRIMIDINES AS UBIQUITIN-SPECIFIC PROTEASE 7 INHIBITORS
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Paragraph 2004; 2006; 2251; 2253, (2016/08/03)
The invention relates to inhibitors of USP7 inhibitors useful in the treatment of cancers, neurodegenerative diseases, immunological disorders, inflammatory disorders, cardiovascular diseases, ischemic diseases, viral infections and diseases, and bacterial infections and diseases, having the Formula: where m, n, X1, X2, R1-R5, R5′ and R6 are described herein.
