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2-chloro-4-nitro-1-((1,1,1-trifluoropropan-2-yl)oxy)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99366-91-3

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99366-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99366-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,6 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99366-91:
(7*9)+(6*9)+(5*3)+(4*6)+(3*6)+(2*9)+(1*1)=193
193 % 10 = 3
So 99366-91-3 is a valid CAS Registry Number.

99366-91-3Downstream Products

99366-91-3Relevant academic research and scientific papers

Optimizing a Weakly Binding Fragment into a Potent ROR?t Inverse Agonist with Efficacy in an in Vivo Inflammation Model

Carcache, David A.,Vulpetti, Anna,Kallen, Joerg,Mattes, Henri,Orain, David,Stringer, Rowan,Vangrevelinghe, Eric,Wolf, Romain M.,Kaupmann, Klemens,Ottl, Johannes,Dawson, Janet,Cooke, Nigel G.,Hoegenauer, Klemens,Billich, Andreas,Wagner, Juergen,Guntermann, Christine,Hintermann, Samuel

, p. 6724 - 6735 (2018/07/21)

The transcription factor ROR?t is an attractive drug-target due to its role in the differentiation of IL-17 producing Th17 cells that play a critical role in the etiopathology of several autoimmune diseases. Identification of starting points for ROR?t inverse agonists with good properties has been a challenge. We report the identification of a fragment hit and its conversion into a potent inverse agonist through fragment optimization, growing and merging efforts. Further analysis of the binding mode revealed that inverse agonism was achieved by an unusual mechanism. In contrast to other reported inverse agonists, there is no direct interaction or displacement of helix 12 observed in the crystal structure. Nevertheless, compound 9 proved to be efficacious in a delayed-type hypersensitivity (DTH) inflammation model in rats.

Regioselective fluoroalkoxylation and polyfluoroalkoxylation of aromatic and heteroaromatic polyhalides

Gupton, John T.,Hertel, George,DeCrescenzo, Gary,Colon, Cesar,Baran, Donna,et al.

, p. 3037 - 3042 (2007/10/02)

A series of activated polyhalobenzenes and polyhaloheteroaromatic compounds have been reacted with a variety of fluoroalkoxide anions.In most cases, regioselective monosubstitution or polysubstitution was observed.The nature of these monosubstitution and polysubstitution reactions is described.

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