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3-Chloro-2-ethoxy-5-nitropyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

874492-07-6

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874492-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874492-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,4,9 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 874492-07:
(8*8)+(7*7)+(6*4)+(5*4)+(4*9)+(3*2)+(2*0)+(1*7)=206
206 % 10 = 6
So 874492-07-6 is a valid CAS Registry Number.

874492-07-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-2-ethoxy-5-nitropyridine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:874492-07-6 SDS

874492-07-6Downstream Products

874492-07-6Relevant 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.

NOVEL COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF FIBROSIS

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Paragraph 0258, (2017/09/15)

The present invention discloses compounds according to Formula I, wherein R1a, R1b, R2a, R2b, R3, R4, R5, R6a, X, Cy1, Cy2, and the subscript n and m are as defined herein. The present invention relates to antagonists compounds of sphingosine 1-phosphate (SIP) receptor, methods for their production, pharmaceutical compositions comprising the same, and methods of treatment using the same, for the prophylaxis and/or treatment of diseases involving fibrotic diseases, inflammatory diseases, autoimmune diseases, metabolic diseases, cardiovascular diseases, and/or proliferative diseases by administering the compound of the invention.

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