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882188-88-7

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882188-88-7 Usage

General Description

1H-Indazole-1-carboxylic acid, 3-formyl-, 1,1-dimethylethyl ester is a chemical compound belonging to the class of organic compounds known as indazoles. Indazoles are polycyclic aromatic compounds containing a pyrazole ring fused to a benzene ring. This particular compound has an ester functional group, which is derived from carboxylic acids and alcohols, along with a formyl group, which is a functional group that consists of a carbonyl bonded to hydrogen. The "1,1-dimethylethyl" portion of its name indicates the presence of a tertiary butyl group. Its molecular formula is C15H17N2O3. Like many other organic compounds, it has potential applications in various research and industrial contexts, though specific information about this particular compound is limited.

Check Digit Verification of cas no

The CAS Registry Mumber 882188-88-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,1,8 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 882188-88:
(8*8)+(7*8)+(6*2)+(5*1)+(4*8)+(3*8)+(2*8)+(1*8)=217
217 % 10 = 7
So 882188-88-7 is a valid CAS Registry Number.

882188-88-7SDS

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 tert-butyl 3-formylindazole-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-Butyl 3-formyl-1H-indazole-1-carboxylate

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:882188-88-7 SDS

882188-88-7Relevant articles and documents

GAMMA-DIKETONES AS WNT/BETA -CATENIN SIGNALING PATHWAY ACTIVATORS

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Paragraph 1755; 1756; 1757; 1760, (2014/09/03)

The present disclosure provides γ-diketones or analogs thereof, that activate Wnt/β-catenin signaling and thus treat or prevent diseases related to signal transduction, such as osteoporosis and osteoarthropathy; osteogenesis imperfecta, bone defects, bone fractures, periodontal disease, otosclerosis, wound healing, craniofacial defects, oncolytic bone disease, traumatic brain injuries or spine injuries, brain atrophy/neurological disorders related to the differentiation and development of the central nervous system, including Parkinson's disease, strokes, ischemic cerebral disease, epilepsy, Alzheimer's disease, depression, bipolar disorder, schizophrenia; otic disorders like cochlear hair cell loss; eye diseases such as age related macular degeneration, diabetic macular edema or retinitis pigmentosa and diseases related to differentiation and growth of stem cell, such as hair loss, hematopoiesis related diseases and tissue regeneration related diseases.

New practical access to 2-azatryptophans and dehydro derivatives via the Wittig-Horner reaction

Crestey, Fran?ois,Collot, Valérie,Stiebing, Silvia,Lohier, Jean-Fran?ois,Santos, Jana Sopkova-de Oliveira,Rault, Sylvain

, p. 2457 - 2460 (2007/10/03)

The Wittig-Horner reaction of protected 3-formylindazoles 1 with (±)-N-(benzyloxycarbonyl)-α-phosphonoglycine trimethyl ester 2 has been developed as a new practical synthesis of dehydro 2-azatryptophans and amino acid derivatives. The preparation of 5-br

Identification of a buried pocket for potent and selective inhibition of Chk1: Prediction and verification

Foloppe, Nicolas,Fisher, Lisa M.,Francis, Geraint,Howes, Rob,Kierstan, Peter,Potter, Andrew

, p. 1792 - 1804 (2007/10/03)

Inhibition of the Chk1 kinase by small molecules binding to its active site is a strategy of great therapeutic interest for oncology. We report how computational modelling predicted the binding mode of ligands of special interest to the Chk1 ATP site, for representatives of an indazole series and debromohymenialdisine. These binding modes were subsequently confirmed by X-ray crystallography. The binding mode of a potent indazole derivative involves non-conventional C-H...O and N-H...π-aromatic interactions with the protein. These interactions are formed in a buried pocket at the periphery of the ATP-binding site, the importance of which has previously been overlooked for ligand design against Chk1. It is demonstrated that filling this pocket can confer ligands with dramatically enhanced affinity for Chk1. Structural arguments in conjunction with assay data explain why targeting this pocket is also advantageous for selective binding to Chk1. Structural overlays of known inhibitors complexed with Chk1 show that only the indazole series utilizes the pocket of interest. Therefore, the analysis presented here should prove helpful in guiding future structure-based ligand design efforts against Chk1.

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