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· · COA & SDS available for every product · Same-day shipping on in-stock items 4-CMTB - Moligand™, ≥97% , CAS No.300851-67-6
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥97% Synonyms
SCHEMBL16369644 | 4-chloro-alpha-(1-methylethyl)-N-2-thiazolylbenzeneacetamide | 4-Chloro-alpha-(1-methylethyl)-N-2-thiazolyl-benzeneacetamide | (+/-)-4-CMTB | Z28173527 | 4-CMTB, >=98% (HPLC) | GTPL5500 | SR-01000025543 | 4-chloro-?-(1-methylethyl)-N-2-t
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥97% Moligand™ 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.
Overview 4-Chloro-α-(1-methylethyl)-N-2-thiazolyl-benzeneacetamide
Specifications Synonyms
SCHEMBL16369644 | 4-chloro-alpha-(1-methylethyl)-N-2-thiazolylbenzeneacetamide | 4-Chloro-alpha-(1-methylethyl)-N-2-thiazolyl-benzeneacetamide | (+/-)-4-CMTB | Z28173527 | 4-CMTB, >=98% (HPLC) | GTPL5500 | SR-01000025543 | 4-chloro-?-(1-methylethyl)-N-2-t
Specifications & Purity
Moligand™, ≥97%
Biochemical and Physiological Mechanisms
4-CMTB is a phenylacetamide compound that acts as an allosteric modulator for the activity of short-chain fatty acid ligand in the FFA2 receptor.
4-CMTB is a potent allosteric agonist of free fatty acid receptor 2 (FFA2).
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 504762955 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504762955 Canonical Smiles CC(C)C(C1=CC=C(C=C1)Cl)C(=O)NC2=NC=CS2 IUPAC Name 2-(4-chlorophenyl)-3-methyl-N-(1,3-thiazol-2-yl)butanamide InChIKey AZYDQCGCBQYFSE-UHFFFAOYSA-N INCHI 1S/C14H15ClN2OS/c1-9(2)12(10-3-5-11(15)6-4-10)13(18)17-14-16-7-8-19-14/h3-9,12H,1-2H3,(H,16,17,18) Isomeric SMILES CC(C)C(C1=CC=C(C=C1)Cl)C(=O)NC2=NC=CS2 Alternate CAS 300851-67-6 Molecular Weight 294.8 Reaxy-Rn 20110673 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=20110673&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 Phenylacetamides Intermediate Tree Nodes Not available Direct Parent Phenylacetamides Alternative Parents Phenylpropanes N-arylamides Chlorobenzenes Fatty amides Aryl chlorides Thiazoles Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Organopnictogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteromonocyclic compounds Substituents Phenylacetamide - Phenylpropane - N-arylamide - Chlorobenzene - Halobenzene - Aryl halide - Fatty acyl - Fatty amide - Aryl chloride - Heteroaromatic compound - Azole - Thiazole - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Carbonyl group - Organic nitrogen compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound Description This compound belongs to the class of organic compounds known as phenylacetamides. These are amide derivatives of phenylacetic acids. 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: 29.48, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 5.9, Max Conc. mM: 20 Molecular Weight 294.800 g/mol XLogP3 4.100 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 4 Exact Mass 294.059 Da Monoisotopic Mass 294.059 Da Topological Polar Surface Area 70.200 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 306.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 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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