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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock HBX 41108 - ≥98%(HPLC) , CAS No.924296-39-9
Synonyms
7-CHLORO-9-OXOINDENO[1,2-B]PYRAZINE-2,3-DICARBONITRILE | HBX 41108 | 9H-Indeno[1,2-b]pyrazine-2,3-dicarbonitrile, 7-chloro-9-oxo- | A903088 | HY-101666 | SCHEMBL1512560 | C7JH7KSP8Z | HBX41108; HBX-41108; HBX 41,108; HBX-41,108; HBX41,108 | 7-Chloro-9-oxo
Shipped In
Ice chest + Ice pads
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonymes
7-CHLORO-9-OXOINDENO[1,2-B]PYRAZINE-2,3-DICARBONITRILE | HBX 41108 | 9H-Indeno[1,2-b]pyrazine-2,3-dicarbonitrile, 7-chloro-9-oxo- | A903088 | HY-101666 | SCHEMBL1512560 | C7JH7KSP8Z | HBX41108; HBX-41108; HBX 41,108; HBX-41,108; HBX41,108 | 7-Chloro-9-oxo
Spécifications et pureté
≥98%(HPLC)
Mécanismes biochimiques et physiologiques
Inhibitor of ubiquitin-specific protease (USP) 7 activity (IC50= 424 nM). Displays uncompetitive inhibition. Also inhibits USP7-mediated p53 deubiquitination (IC50= 0.8μM). Stabilizes p53 and inhibits cancer cell growth; induces p53-dependent apoptosis in
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504768021
Sourires canoniques
C1=CC2=C(C=C1Cl)C(=O)C3=NC(=C(N=C23)C#N)C#N
IUPAC Name
7-chloro-9-oxoindeno[1,2-b]pyrazine-2,3-dicarbonitrile
InChIKey
BIGPXXAUSQLTQR-UHFFFAOYSA-N
INCHI
1S/C13H3ClN4O/c14-6-1-2-7-8(3-6)13(19)12-11(7)17-9(4-15)10(5-16)18-12/h1-3H
Isomères SMILES
C1=CC2=C(C=C1Cl)C(=O)C3=NC(=C(N=C23)C#N)C#N
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=12774588&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic oxygen compounds Classe Organooxygen compounds Subclass Carbonyl compounds Intermediate Tree Nodes Ketones Direct Parent Aryl ketones Alternative Parents Pyrazines Benzenoids Aryl chlorides Heteroaromatic compounds Nitriles Azacyclic compounds Organochlorides Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Aryl ketone - Aryl chloride - Aryl halide - Pyrazine - Benzenoid - Heteroaromatic compound - Organoheterocyclic compound - Nitrile - Carbonitrile - Azacycle - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organochloride - Organohalogen compound - Cyanide - Organic nitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as aryl ketones. These are organic aromatic compounds that contain a ketone group substituted at one C-atom with an aryl group. They have the generic structure RC(=O)R', where R = aryl group and R'=organyl group. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Structure 3D Cibles associées (humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Solubilité Solvent:DMSO, Max Conc. mg/mL: 26.66, Max Conc. mM: 100 Sensibilité Moisture sensitive Poids moléculaire 266.640 g/mol XLogP3 2.000 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 0 Exact Mass 266 Da Monoisotopic Mass 266 Da Topological Polar Surface Area 90.400 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 503.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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