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· · COA & SDS available for every product · Same-day shipping on in-stock items OAC-2 - ≥98%(HPLC) , CAS No.6019-39-2
Synonyms
MLS000860608 | JCAFGYWSIWYMOX-UHFFFAOYSA-N | EX-A906 | J-690331 | SMR000458692 | 6-[(2-Amino-4-pyrimidinyl)oxy]-N-[3-(trifluoromethyl)phenyl]-1-naphthamide | A914514 | OAC-2;OAC 2 | SCHEMBL4761937 | DTXSID301329745 | EN300-7401519 | 5-benzoylaminoindole |
Storage
Store at -20°C,Argon charged
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,Argon charged 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 Synonyms
MLS000860608 | JCAFGYWSIWYMOX-UHFFFAOYSA-N | EX-A906 | J-690331 | SMR000458692 | 6-[(2-Amino-4-pyrimidinyl)oxy]-N-[3-(trifluoromethyl)phenyl]-1-naphthamide | A914514 | OAC-2;OAC 2 | SCHEMBL4761937 | DTXSID301329745 | EN300-7401519 | 5-benzoylaminoindole |
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
OAC2 (Oct4 activating compound 2) is an activator of Octamer-binding transcription factor 4 (Oct4), which is involved in the self-renewal of undifferentiated embryonic stem cells, regulating embryonic stem cell pluripotency.
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 504762205 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504762205 Canonical Smiles C1=CC=C(C=C1)C(=O)NC2=CC3=C(C=C2)NC=C3 IUPAC Name N-(1H-indol-5-yl)benzamide InChIKey JCAFGYWSIWYMOX-UHFFFAOYSA-N INCHI 1S/C15H12N2O/c18-15(11-4-2-1-3-5-11)17-13-6-7-14-12(10-13)8-9-16-14/h1-10,16H,(H,17,18) Isomeric SMILES C1=CC=C(C=C1)C(=O)NC2=CC3=C(C=C2)NC=C3 Molecular Weight 236.27 Reaxy-Rn 194144 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=194144&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 Organoheterocyclic compounds Class Indoles and derivatives Subclass Indoles Intermediate Tree Nodes Not available Direct Parent Indoles Alternative Parents Benzamides Benzoyl derivatives Pyrroles Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Benzamide - Benzoic acid or derivatives - Indole - Benzoyl - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Pyrrole - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. 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: 23.63, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 23.63, Max Conc. mM: 100 Melt Point(°C) 165 - 167°C Molecular Weight 236.270 g/mol XLogP3 2.700 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 2 Exact Mass 236.095 Da Monoisotopic Mass 236.095 Da Topological Polar Surface Area 44.900 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 299.000 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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