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340,000+ research products · Triple ISO certified · COA & SDS available for every product · Same-day shipping on in-stock items Cycloate - analytical standard , CAS No.1134-23-2
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. Synonyms
Ro-Neet 6E|Ro-Neet 6-E|S-Ethyl (cyclohexyl)ethylthiocarbamate|Carbamic acid, cyclohexylethylthio-, S-ethyl ester|S-Ethyl cyclohexyl(ethyl)carbamothioate|CYCLOATE|CYCLOATE [HSDB]|Sabet|Cycloate [ISO]|S-Ethyl N-cyclohexyl-N-ethylthiocarbamate|Ro-Neet 10G|Ethyl cyclohexylethylthiocarbamate|S-Ethyl N-cyclohexyl-N-ethyl(thiocarbamate)|R 2063|R-2063|Ronit|Etsan|Cycloate [BSI:ISO]|Eurex|S-Ethyl cyclohexylethylthiocarbamate|S-Ethylethylcyclohexylthiocarbamate|Ethyl 2-((2-aminoethyl)thio)-2-ethylbutanoate|S-Ethyl cyclohexylethylcarbamothioate|S-Ethyl N-ethyl-N-cyclohexylthiocarbamate|S-Ethyl N-ethyl-N-cyclohexyl-thiocarbamate|Carbamothioic acid, cyclohexylethyl-, S-ethyl ester|Ro-Neet E|Carbamothioic acid, N-cyclohexyl-N-ethyl-, S-ethyl ester|Ethyl N-cyclohexyl-N-ethylthiolcarbamate|S-Ethyl N-cyclohexylthiocarbamate|S-Ethyl N-ethylcyclohexanecarbamothioate|Cyclohexanecarbamic acid, N-ethylthio-, S-ethyl ester|S-ethyl N-cyclohexyl-N-ethylcarbamothioate|S-Ethyl N-ethyl-N-cyclohexylthiolcarbamate|Ro-Neet|S-Ethyl N-ethylthiocyclohexanecarbamate
Specifications Synonyms
Ro-Neet 6E | Ro-Neet 6-E | S-Ethyl (cyclohexyl)ethylthiocarbamate | Carbamic acid, cyclohexylethylthio-, S-ethyl ester | S-Ethyl cyclohexyl(ethyl)carbamothioate | CYCLOATE | CYCLOATE [HSDB] | Sabet | Cycloate [ISO] | S-Ethyl N-cyclohexyl-N-ethylthiocarbamate | Ro-Neet 10G | Ethyl cyclohexylethylthiocarbamate | S-Ethyl N-cyclohexyl-N-ethyl Show more
Specifications & Purity
analytical standard
Names and Identifiers Canonical Smiles
CCN(C1CCCCC1)C(=O)SCC
IUPAC Name
S-ethyl N-cyclohexyl-N-ethylcarbamothioate
InChIKey
DFCAFRGABIXSDS-UHFFFAOYSA-N
INCHI
1S/C11H21NOS/c1-3-12(11(13)14-4-2)10-8-6-5-7-9-10/h10H,3-9H2,1-2H3
Isomeric SMILES
CCN(C1CCCCC1)C(=O)SCC
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2937178&ln=
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organosulfur compounds Class Thiocarbonyl compounds Subclass Thiocarbamic acid derivatives Intermediate Tree Nodes Not available Direct Parent Thiocarbamic acid derivatives Alternative Parents Organic carbonic acids and derivatives Sulfenyl compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic homomonocyclic compounds Substituents Thiocarbamic acid derivative - Carbonic acid derivative - Sulfenyl compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as thiocarbamic acid derivatives. These are organic compounds containing a functional group with the general structure OC(=S)NR2 or SC(=O)NR2. External Descriptors Thiocarbamate herbicides 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) Mechanisms of Action Certificates (CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Flash Point(°F) >100 °C Flash Point(°C) >100°C Molecular Weight 215.360 g/mol XLogP3 4.100 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 4 Exact Mass 215.134 Da Monoisotopic Mass 215.134 Da Topological Polar Surface Area 45.600 Ų Heavy Atom Count 14 Formal Charge 0 Complexity 178.000 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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