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GRADE & PURITY ≥99% esterase substrate Synonyms
1H-Indol-3-ol,5-bromo-4-chloro-,3-acetate | 5-Bromo-4-chloro-3-indolyl acetate | TD8107 | SY021723 | SCHEMBL154466 | (5-bromo-4-chloro-1H-indol-3-yl) acetate | 3-Acetoxy-4-chloro-5-bromoindole | B-6244 | B4830 | HY-52112 | 1H-Indol-3-ol, 5-bromo-4-chloro-
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
Overview A histochemical substrate for esterase.
Specifications Synonyms
1H-Indol-3-ol, 5-bromo-4-chloro-, 3-acetate | 5-Bromo-4-chloro-3-indolyl acetate | TD8107 | SY021723 | SCHEMBL154466 | (5-bromo-4-chloro-1H-indol-3-yl) acetate | 3-Acetoxy-4-chloro-5-bromoindole | B-6244 | B4830 | HY-52112 | 1H-Indol-3-ol, 5-bromo-4-chloro-
Specifications & Purity
≥99%, esterase substrate
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 Canonical Smiles CC(=O)OC1=CNC2=C1C(=C(C=C2)Br)Cl IUPAC Name (5-bromo-4-chloro-1H-indol-3-yl) acetate InChIKey WPWLFFMSSOAORQ-UHFFFAOYSA-N INCHI 1S/C10H7BrClNO2/c1-5(14)15-8-4-13-7-3-2-6(11)10(12)9(7)8/h2-4,13H,1H3 Isomeric SMILES CC(=O)OC1=CNC2=C1C(=C(C=C2)Br)Cl WGK Germany 3 Molecular Weight 288.53 Reaxy-Rn 199004 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=199004&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 Substituted pyrroles Benzenoids Aryl chlorides Aryl bromides Heteroaromatic compounds Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organochlorides Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Indole - Aryl bromide - Aryl chloride - Aryl halide - Substituted pyrrole - Benzenoid - Pyrrole - Heteroaromatic compound - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Azacycle - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organobromide - Organohalogen compound - Organic oxide - Carbonyl group - 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 Certificates(CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity Air & Light & Heat sensitive Melt Point(°C) 107 °C(dec.) Molecular Weight 288.520 g/mol XLogP3 3.100 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 2 Exact Mass 286.935 Da Monoisotopic Mass 286.935 Da Topological Polar Surface Area 42.100 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 264.000 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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