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3,5-difluoro-4-methoxybenzohydrazide is a chemical compound with the molecular formula C8H7F2N2O2. It is a derivative of benzohydrazide, featuring a benzene ring with two fluorine atoms at the 3rd and 5th positions, a methoxy group at the 4th position, and a hydrazide functional group. 3,5-difluoro-4-methoxybenzohydrazide is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain active ingredients. Its structure allows for the exploration of its properties in medicinal chemistry, such as its potential to inhibit specific enzymes or bind to receptors, which could be valuable in the development of new drugs. The compound's synthesis and reactivity are of interest to researchers in the field of organic chemistry, as it may offer insights into the behavior of similar compounds with fluorine and methoxy substituents.

455-55-0

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455-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 455-55-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 455-55:
(5*4)+(4*5)+(3*5)+(2*5)+(1*5)=70
70 % 10 = 0
So 455-55-0 is a valid CAS Registry Number.

455-55-0Relevant academic research and scientific papers

Aromatic sulfonyl fluorides covalently kinetically stabilize transthyretin to prevent amyloidogenesis while affording a fluorescent conjugate

Grimster, Neil P.,Connelly, Stephen,Baranczak, Aleksandra,Dong, Jiajia,Krasnova, Larissa B.,Sharpless, K. Barry,Powers, Evan T.,Wilson, Ian A.,Kelly, Jeffery W.

supporting information, p. 5656 - 5668 (2013/06/04)

Molecules that bind selectively to a given protein and then undergo a rapid chemoselective reaction to form a covalent conjugate have utility in drug development. Herein a library of 1,3,4-oxadiazoles substituted at the 2 position with an aryl sulfonyl fluoride and at the 5 position with a substituted aryl known to have high affinity for the inner thyroxine binding subsite of transthyretin (TTR) was conceived of by structure-based design principles and was chemically synthesized. When bound in the thyroxine binding site, most of the aryl sulfonyl fluorides react rapidly and chemoselectively with the pK a-perturbed K15 residue, kinetically stabilizing TTR and thus preventing amyloid fibril formation, known to cause polyneuropathy. Conjugation t50s range from 1 to 4 min, ~1400 times faster than the hydrolysis reaction outside the thyroxine binding site. X-ray crystallography confirms the anticipated binding orientation and sheds light on the sulfonyl fluoride activation leading to the sulfonamide linkage to TTR. A few of the aryl sulfonyl fluorides efficiently form conjugates with TTR in plasma. Eleven of the TTR covalent kinetic stabilizers synthesized exhibit fluorescence upon conjugation and therefore could have imaging applications as a consequence of the environment sensitive fluorescence of the chromophore.

Triazole derivatives

-

, (2011/03/17)

The present invention relates to triazole and imidazole derivatives of formula I and to their pharmaceutically acceptable acid addition salts. These compounds are NMDA receptor subtype blockers and are useful for the treatment of diseases related to the NMDA receptor.

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