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· · COA & SDS available for every product · Same-day shipping on in-stock items FGIN-1-43 - ≥98% , CAS No.145040-29-5
Synonyms
BDBM50045882 | HMS3675M18 | J-008043 | SR-01000597647 | Tocris-0659 | 1H-Indole-3-acetamide, 5-chloro-2-(4-chlorophenyl)-N,N-dihexyl- | C68RF62SNJ | DTXSID50398444 | BRD-K66093087-001-02-3 | 2-[5-Chloro-2-(4-chloro-phenyl)-1H-indol-3-yl]-N,N-dihexyl-aceta
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% 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 Synonyms
BDBM50045882 | HMS3675M18 | J-008043 | SR-01000597647 | Tocris-0659 | 1H-Indole-3-acetamide, 5-chloro-2-(4-chlorophenyl)-N, N-dihexyl- | C68RF62SNJ | DTXSID50398444 | BRD-K66093087-001-02-3 | 2-[5-Chloro-2-(4-chloro-phenyl)-1H-indol-3-yl]-N, N-dihexyl-aceta
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
Most active of the 2-aryl-3-indoleacetamides; a new class of potent and specific ligands as probes for the mitochondial DBI receptor (peripheral benzodiazepine receptor).
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 504762804 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504762804 Canonical Smiles CCCCCCN(CCCCCC)C(=O)CC1=C(NC2=C1C=C(C=C2)Cl)C3=CC=C(C=C3)Cl IUPAC Name 2-[5-chloro-2-(4-chlorophenyl)-1H-indol-3-yl]-N,N-dihexylacetamide InChIKey XTZUPNNVXIMWAR-UHFFFAOYSA-N INCHI 1S/C28H36Cl2N2O/c1-3-5-7-9-17-32(18-10-8-6-4-2)27(33)20-25-24-19-23(30)15-16-26(24)31-28(25)21-11-13-22(29)14-12-21/h11-16,19,31H,3-10,17-18,20H2,1-2H3 Isomeric SMILES CCCCCCN(CCCCCC)C(=O)CC1=C(NC2=C1C=C(C=C2)Cl)C3=CC=C(C=C3)Cl Molecular Weight 487.51 Reaxy-Rn 6617216 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6617216&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 2-phenylindoles Alternative Parents Phenylpyrroles 3-alkylindoles Chlorobenzenes Aryl chlorides Tertiary carboxylic acid amides Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents 2-phenylindole - 2-phenylpyrrole - 3-alkylindole - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Substituted pyrrole - Benzenoid - Tertiary carboxylic acid amide - Heteroaromatic compound - Pyrrole - Carboxamide group - Azacycle - Carboxylic acid derivative - Organopnictogen compound - Organochloride - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as 2-phenylindoles. These are indoles substituted at the 2-position with a phenyl 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: 24.37, Max Conc. mM: 50 Molecular Weight 487.500 g/mol XLogP3 9.000 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 13 Exact Mass 486.22 Da Monoisotopic Mass 486.22 Da Topological Polar Surface Area 36.100 Ų Heavy Atom Count 33 Formal Charge 0 Complexity 554.000 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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