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1,1,1-trifluoro-2-hydroxy-2-(2-aminophenyl)ethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

205756-49-6

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205756-49-6 Usage

Type

Synthetic thyroid hormone

Structural Similarity

Similar to naturally occurring hormone thyroxine

Purpose

Treats hypothyroidism (low thyroid hormone production)

Mechanism of Action

Replaces missing hormone, regulates energy and metabolism

Form

Oral medication

Administration

Once a day on an empty stomach

Time to Effect

Full effects take several weeks

Side Effects

Hair loss, weight loss, tremors, irritability

Drug Interactions

May interact with other medications

Consultation

Important to consult healthcare professional before starting or stopping treatment

Check Digit Verification of cas no

The CAS Registry Mumber 205756-49-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,7,5 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 205756-49:
(8*2)+(7*0)+(6*5)+(5*7)+(4*5)+(3*6)+(2*4)+(1*9)=136
136 % 10 = 6
So 205756-49-6 is a valid CAS Registry Number.

205756-49-6Relevant academic research and scientific papers

Fluorescence "turn-on" sensing of carboxylate anions with oligothiophene-based o-(carboxamido)trifluoroacetophenones

Kim, Dae-Sik,Kyo, Han Ahn

, p. 6831 - 6834 (2008/12/22)

(Chemical Equation Presented) o-(Carboxamido)trifluoroacetophenones containing ter- or pentathiophene moiety as a fluorophore exhibit fluorescence enhancement upon binding carboxylate anions. Particularly, the terthiophene derivative shows a large fluorescence enhancement factor (FEF = 120). The enhancement is explained by intramolecular H-bonding stabilization of an anion-ionophore adduct, through which a possible quenching process, the n-π* transition from the trifluoroacetophenone moiety, is eliminated.

Fluorescence modulation in anion sensing by introducing intramolecular H-bonding interactions in host-guest adducts

Chung, Yun Mi,Raman, Balamurali,Kim, Dae-Sik,Ahn, Kyo Han

, p. 186 - 188 (2008/02/08)

Fluorescence signaling in anion binding is modulated from quenching to enhancement by intramolecular H-bonding stabilization of anion-ionophore adducts; the intramolecular H-bonding is suggested to suppress the quenching processes otherwise possible and i

Electrophilic ketones for the treatment of herpesvirus infections

-

, (2008/06/13)

A class of compounds is described which can be used for the treatment of viral infections. Compounds of particular interest are defined by Formula II wherein each of R1, R2, and R3 is independently selected from hydrido, h

4,4-DISUBSTITUTED-1,4-DIHYDRO-2H-3,1-BENZOXAZIN-2-ONES USEFUL AS HIV REVERSE TRANSCRIPTASE INHIBITORS AND INTERMEDIATES AND PROCESSES FOR MAKING THE SAME

-

, (2008/06/13)

The present invention relates to benzoxazinones of formula I, or stereoisomeric forms or mixtures, or pharmaceutically acceptable salt forms thereof, which are useful as inhibitors of HIV reverse transcriptase, and to pharmaceutical compositions and diagnostic kits comprising the same, methods of using same for treating viral infection or as an assay standard or reagent, and intermediates and processes for making the same.

Synthesis and evaluation of analogs of Efavirenz (SUSTIVA(TM)) as HIV-1 reverse transcriptase inhibitors

Patel, Mona,Ko, Soo S.,McHugh Jr., Robert J.,Markwalder, Jay A.,Srivastava, Anurag S.,Cordova, Beverly C.,Klabe, Ronald M.,Erickson-Viitanen, Susan,Trainor, George L.,Seitz, Steven P.

, p. 2805 - 2810 (2007/10/03)

Efavirenz (SUSTIVA(TM)) is a potent non-nucleoside reverse transcriptase inhibitor. Due to the observation of breakthrough mutations of the reverse transcriptase enzyme during Efavirenz therapy, we sought to develop an optimized second generation series. To that end, SAR of the substituents on the aromatic ring was undertaken and the results are summarized here. The 5,6-difluoro (4f) and the 6-methoxy (4m) substituted benzoxazinones were determined to be equipotent, and as a result such substitution patterns will be incorporated in second generation scaffolds.

4,4-disubstitued-1,4-dihydro-2H-3,1-benzoxazin-2-ones useful as HIV reverse transcriptase inhibitors and intermediates and processes for making the same

-

, (2008/06/13)

The present invention relates to benzoxazinones of formula I: STR1 or stereoisomeric forms or mixtures, or pharmaceutically acceptable salt forms thereof, which are useful as inhibitors of HIV reverse transcriptase, and to pharmaceutical compositions and diagnostic kits comprising the same, methods of using the same for treating viral infection or as an assay standard or reagent, and intermediates and processes for making the same.

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