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· · COA & SDS available for every product · Same-day shipping on in-stock items Unii-4T71DC0G0A , Tyrosine-protein kinase JAK2 inhibitor, CAS No.937273-04-6, Tyrosine-protein kinase JAK2 inhibitor
Synonyms
SB-1578 | SCHEMBL17594734 | CHEMBL2035185 | 7,12,26-TRIOXA-19,21,24-TRIAZATETRACYCLO(18.3.1.12,5.114,18)HEXACOSA-1(24),2,4,9,14,16,18(25),20,22-NONAENE, 15-(2-(1-PYRROLIDINYL)ETHOXY)-, (9E)- | 4T71DC0G0A | DB15294 | CT-1578 | SB1578 | NSC772920 | ONX-0805
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Why this grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships 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 Synonyms
SB-1578 | SCHEMBL17594734 | CHEMBL2035185 | 7, 12, 26-TRIOXA-19, 21, 24-TRIAZATETRACYCLO(18.3.1.12, 5.114, 18)HEXACOSA-1(24), 2, 4, 9, 14, 16, 18(25), 20, 22-NONAENE, 15-(2-(1-PYRROLIDINYL)ETHOXY)-, (9E)- | 4T71DC0G0A | DB15294 | CT-1578 | SB1578 | NSC772920 | ONX-0805
Mechanism of action
Tyrosine-protein kinase JAK2 inhibitor
Product Properties Names and Identifiers Canonical Smiles C1CCN(C1)CCOC2=C3COCC=CCOCC4=CC=C(O4)C5=NC(=NC=C5)NC(=C3)C=C2 IUPAC Name (9E)-15-(2-pyrrolidin-1-ylethoxy)-7,12,26-trioxa-19,21,24-triazatetracyclo[18.3.1.12,5.114,18]hexacosa-1(24),2,4,9,14,16,18(25),20,22-nonaene InChIKey NNXDIGHYPZHXTR-ONEGZZNKSA-N INCHI 1S/C26H30N4O4/c1-2-12-30(11-1)13-16-33-24-7-5-21-17-20(24)18-31-14-3-4-15-32-19-22-6-8-25(34-22)23-9-10-27-26(28-21)29-23/h3-10,17H,1-2,11-16,18-19H2,(H,27,28,29)/b4-3+ Isomeric SMILES C1CCN(C1)CCOC2=C3COC/C=C/COCC4=CC=C(O4)C5=NC(=NC=C5)NC(=C3)C=C2 PubChem CID 16750271 Molecular Weight 462.5
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.
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View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Class Phenol ethers Subclass Not available Intermediate Tree Nodes Not available Direct Parent Phenol ethers Alternative Parents Alkyl aryl ethers Pyrimidines and pyrimidine derivatives N-alkylpyrrolidines Heteroaromatic compounds Furans Trialkylamines Oxacyclic compounds Dialkyl ethers Azacyclic compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Phenol ether - Alkyl aryl ether - Pyrimidine - N-alkylpyrrolidine - Furan - Pyrrolidine - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Ether - Dialkyl ether - Organoheterocyclic compound - Azacycle - Oxacycle - Amine - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. 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.
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