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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Iso-H7 dihydrochloride - 10mM in DMSO , CAS No.140663-38-3
GRADE & PURITY 10mM in DMSO
Synonyms
140663-38-3|1-(5-Isoquinolinylsulfonyl)-3-methylpiperazine dihydrochloride|Iso-H7 dihydrochloride|Iso-H-7|1-(5-ISOQUINOLINYLSULFONYL)-3-METHYL-PIPERAZINE DIHYDROCHLORIDE|5-((3-METHYLPIPERAZIN-1-YL)SULFONYL)ISOQUINOLINE 2HCL|5-(3-methylpiperazin-1-yl)sulfo
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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.
Descripción general Information
Iso-H7 dihydrochloride Iso-H7 dihydrochloride is an inhibitor of phosphokinase C .
Specifications Sinónimos
140663-38-3 | 1-(5-Isoquinolinylsulfonyl)-3-methylpiperazine dihydrochloride | Iso-H7 dihydrochloride | Iso-H-7 | 1-(5-ISOQUINOLINYLSULFONYL)-3-METHYL-PIPERAZINE DIHYDROCHLORIDE | 5-((3-METHYLPIPERAZIN-1-YL)SULFONYL)ISOQUINOLINE 2HCL | 5-(3-methylpiperazin-1-yl)sulfo
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Iso-H7 dihydrochloride is an inhibitor of phosphokinase C.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Propiedades del producto ALogP 1.267 Recuento HBD 1 Enlace rotable 2
Nombres e identificadores Sonrisas canónicas CC1CN(CCN1)S(=O)(=O)C2=CC=CC3=C2C=CN=C3.Cl.Cl IUPAC Name 5-(3-methylpiperazin-1-yl)sulfonylisoquinoline;dihydrochloride InChIKey YHYNDFTUZMEYNX-UHFFFAOYSA-N INCHI 1S/C14H17N3O2S.2ClH/c1-11-10-17(8-7-16-11)20(18,19)14-4-2-3-12-9-15-6-5-13(12)14;;/h2-6,9,11,16H,7-8,10H2,1H3;2*1H Isómeros SMILES CC1CN(CCN1)S(=O)(=O)C2=CC=CC3=C2C=CN=C3.Cl.Cl PubChem CID 11957580 Peso molecular 364.29
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 Organoheterocyclic compounds Clase Isoquinolines and derivatives Subclass Not available Intermediate Tree Nodes Not available Direct Parent Isoquinolines and derivatives Alternative Parents Pyridines and derivatives Piperazines Organosulfonamides Benzenoids Sulfonyls Heteroaromatic compounds Dialkylamines Azacyclic compounds Organic oxides Hydrochlorides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Isoquinoline - 1,4-diazinane - Piperazine - Pyridine - Benzenoid - Organosulfonic acid amide - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Secondary aliphatic amine - Secondary amine - Azacycle - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrochloride - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as isoquinolines and derivatives. These are aromatic polycyclic compounds containing an isoquinoline moiety, which consists of a benzene ring fused to a pyridine ring and forming benzo[c]pyridine. 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.
Estructura 3D Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas DMSO (mg/ml) Solubilidad máxima 73 DMSO (mM) Solubilidad máxima 200.389799335694 Agua (mg/ml) Solubilidad máxima 73 Agua (mM) Solubilidad máxima 200.389799335694 Peso molecular 364.300 g/mol XLogP3 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 2 Exact Mass 363.058 Da Monoisotopic Mass 363.058 Da Topological Polar Surface Area 70.700 Ų Heavy Atom Count 22 Formal Charge 0 Complexity 434.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 3
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