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· · COA & SDS available for every product · Same-day shipping on in-stock items KY02111 - 10mM in DMSO , CAS No.1118807-13-8
GRADE & PURITY 10mM in DMSO
Synonyms
EN300-1266069 | UNII-6AXH36YF6M | AS-16445 | DTXSID80429194 | MFCD08483062 | KY02111 | KY-02111 | UNII-A4125MQ8RX | 2-(3-(3,4-Dimethoxyphenyl)propanamido)-6-chlorobenzothiazole | S7096 | AM81229 | C18H17ClN2O3S | N-(6-Chloro-benzothiazol-2-yl)-3-(3,4-dime
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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.
Overview KY02111 promotes differentiation of hPSCs to cardiomyocytes by inhibiting Wnt signaling, may act downstream of APC and GSK3β.
Specifications Synonyms
EN300-1266069 | UNII-6AXH36YF6M | AS-16445 | DTXSID80429194 | MFCD08483062 | KY02111 | KY-02111 | UNII-A4125MQ8RX | 2-(3-(3,4-Dimethoxyphenyl)propanamido)-6-chlorobenzothiazole | S7096 | AM81229 | C18H17ClN2O3S | N-(6-Chloro-benzothiazol-2-yl)-3-(3,4-dime
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
KY02111 promotes differentiation of human pluripotent stem cells (hPSCs) to cardiomyocytes by inhibiting WNT signaling in hPSCs in a manner that is distinct from that of previously studied WNT inhibitors. The substantial (98%) differentiation of hPSCs to
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles
COC1=C(C=C(C=C1)CCC(=O)NC2=NC3=C(S2)C=C(C=C3)Cl)OC
IUPAC Name
N-(6-chloro-1,3-benzothiazol-2-yl)-3-(3,4-dimethoxyphenyl)propanamide
InChIKey
LXFKEVQQSKQXPR-UHFFFAOYSA-N
INCHI
1S/C18H17ClN2O3S/c1-23-14-7-3-11(9-15(14)24-2)4-8-17(22)21-18-20-13-6-5-12(19)10-16(13)25-18/h3,5-7,9-10H,4,8H2,1-2H3,(H,20,21,22)
Isomeric SMILES
COC1=C(C=C(C=C1)CCC(=O)NC2=NC3=C(S2)C=C(C=C3)Cl)OC
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=23763295&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 Methoxybenzenes Intermediate Tree Nodes Not available Direct Parent Dimethoxybenzenes Alternative Parents Benzothiazoles Phenoxy compounds N-arylamides Anisoles Alkyl aryl ethers Fatty amides Aryl chlorides Thiazoles Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents O-dimethoxybenzene - Dimethoxybenzene - 1,3-benzothiazole - Phenoxy compound - Anisole - Phenol ether - N-arylamide - Alkyl aryl ether - Aryl chloride - Aryl halide - Fatty amide - Fatty acyl - Heteroaromatic compound - Azole - Thiazole - Carboxamide group - Secondary carboxylic acid amide - Ether - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Organohalogen compound - Organochloride - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as dimethoxybenzenes. These are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups. 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(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Molecular Weight 376.900 g/mol XLogP3 4.300 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 6 Exact Mass 376.065 Da Monoisotopic Mass 376.065 Da Topological Polar Surface Area 88.700 Ų Heavy Atom Count 25 Formal Charge 0 Complexity 456.000 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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