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2-Propenoic acid, 3-[2-fluoro-4-(trifluoromethyl)phenyl]-, (2E)- is a complex organic chemical compound with the molecular formula C10H6F4O2. It is characterized by a 2-propenoic acid backbone, which features a double bond between the second and third carbon atoms. The molecule also contains a 2-fluoro-4-(trifluoromethyl)phenyl group attached to the third carbon of the propenoic acid chain. This group consists of a benzene ring with a fluorine atom at the 2-position and a trifluoromethyl group (-CF3) at the 4-position. The compound is a specific geometric isomer, with the E configuration indicating the arrangement of the fluorine and trifluoromethyl groups relative to the double bond. This chemical is primarily used in the synthesis of pharmaceuticals and other specialty chemicals, owing to its unique structure and reactivity.

545393-87-1

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545393-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 545393-87-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,5,3,9 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 545393-87:
(8*5)+(7*4)+(6*5)+(5*3)+(4*9)+(3*3)+(2*8)+(1*7)=181
181 % 10 = 1
So 545393-87-1 is a valid CAS Registry Number.

545393-87-1Downstream Products

545393-87-1Relevant academic research and scientific papers

Hydroxamic acids block replication of hepatitis c virus

Ai, Teng,Xu, Yanli,Qiu, Li,Geraghty, Robert J.,Chen, Liqiang

, p. 785 - 800 (2015/01/30)

Intrigued by the role of protein acetylation in hepatitis C virus (HCV) replication, we tested known histone deacetylase (HDAC) inhibitors and a focused library of structurally simple hydroxamic acids for inhibition of a HCV subgenomic replicon. While known HDAC inhibitors with varied inhibitory profiles proved to be either relatively toxic or ineffective, structure-activity relationship (SAR) studies on cinnamic hydroxamic acid and benzo[b]thiophen-2-hydroxamic acid gave rise to compounds 22 and 53, which showed potent and selective anti-HCV activity and therefore are promising starting points for further structural optimization and mechanistic studies.

Amides of aminoalkyl-substituted azetidines, pyrrolidines, piperidines and azepanes

-

, (2008/06/13)

Novel amides of aminoalkyl-substituted azetidines, pyrrolidines, piperidines and azepanes, use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds, and a method of treatment employing these compounds and compositions. The compounds show a high and selective binding affinity to the histamine H3 receptor indicating histamine H3 receptor antagonistic, inverse agonistic or agonistic activity. As a result, the compounds are useful for the treatment of diseases and disorders related to the histamine H3 receptor.

Vanilloid receptor ligands and their use in treatments

-

, (2008/06/13)

Compounds having the general structure and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritis, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.

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