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· · COA & SDS available for every product · Same-day shipping on in-stock items OUL35 - ≥98%(HPLC) , CAS No.6336-34-1
Synonyms
NSC39047 | HMS2754A23 | OUL 35 | NSC39047 | NSC-39047 | SR-01000391101-1 | AKOS001482413 | DTXSID10284793 | SCHEMBL3137816 | HMS1415F19 | SMR000393949 | 4-(4-carbamoylphenoxy)benzamide | 4,4'-oxydibenzamide | 4-(4-aminocarbonylphenoxy)benzamide | MS-23611
Storage
Store at 2-8°C,Protected from light
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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 2-8°C,Protected from light Ships Wet ice 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
NSC39047 | HMS2754A23 | OUL 35 | NSC39047 | NSC-39047 | SR-01000391101-1 | AKOS001482413 | DTXSID10284793 | SCHEMBL3137816 | HMS1415F19 | SMR000393949 | 4-(4-carbamoylphenoxy)benzamide | 4, 4'-oxydibenzamide | 4-(4-aminocarbonylphenoxy)benzamide | MS-23611
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
Selective PARP-10 (also known as ADP-ribosyltransferase Diptheria Toxin-like 10, ARTD10) inhibitor (IC50= 0.329 μM). Displays selectivity for PARP-10 over a panel of PARP family members. Rescues HeLa cells from PARP-10-induced cell death. Sensitizes cance
Storage
Store at 2-8°C, Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles C1=CC(=CC=C1C(=O)N)OC2=CC=C(C=C2)C(=O)N IUPAC Name 4-(4-carbamoylphenoxy)benzamide InChIKey XZRCQWLPMXFGHE-UHFFFAOYSA-N INCHI 1S/C14H12N2O3/c15-13(17)9-1-5-11(6-2-9)19-12-7-3-10(4-8-12)14(16)18/h1-8H,(H2,15,17)(H2,16,18) Isomeric SMILES C1=CC(=CC=C1C(=O)N)OC2=CC=C(C=C2)C(=O)N Molecular Weight 256.26 Reaxy-Rn 2859503 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2859503&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 Benzenoids Class Benzene and substituted derivatives Subclass Diphenylethers Intermediate Tree Nodes Not available Direct Parent Diphenylethers Alternative Parents Diarylethers Benzamides Phenoxy compounds Phenol ethers Benzoyl derivatives Primary carboxylic acid amides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Diphenylether - Diaryl ether - Benzamide - Benzoic acid or derivatives - Phenoxy compound - Benzoyl - Phenol ether - Carboxamide group - Primary carboxylic acid amide - Ether - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 25.63, Max Conc. mM: 100 Sensitivity Light sensitive Molecular Weight 256.260 g/mol XLogP3 1.200 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 4 Exact Mass 256.085 Da Monoisotopic Mass 256.085 Da Topological Polar Surface Area 95.400 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 298.000 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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