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· · COA & SDS available for every product · Same-day shipping on in-stock items Cyclohexanone oxime - ≥97% , CAS No.100-64-1
Synonyms
(HYDROXYIMINO)CYCLOHEXANE|Cyclohexanone oxime|hydroxyiminocyclohexane|Cyclohexanone, oxime|Cyclo-hexanone, oxime|Benzenepropanoic acid, 3-chloro-.alpha.-oxo-|cyclohexan-1-one oxime|cyclohexanoneoxime|(HYDROXYIMINO)CYCLOHEXANE [HSDB]|cyclohexanone oxime;cyclohexanone, oxime;n-hydroxycyclohexanimine;cyclohexanone oxime cyclohexanone, oxime n-hydroxycyclohexanimine|N-cyclohexylidenehydroxylamine|N-cyclohexylidene-hydroxylamine|Cyclohexanoneoxime(Chunks or pellets)
Specifications Synonyms
(HYDROXYIMINO)CYCLOHEXANE | Cyclohexanone oxime | hydroxyiminocyclohexane | Cyclohexanone, oxime | Cyclo-hexanone, oxime | Benzenepropanoic acid, 3-chloro-.alpha.-oxo- | cyclohexan-1-one oxime | cyclohexanoneoxime | (HYDROXYIMINO)CYCLOHEXANE [HSDB] | cyclohexanone oxime;cyclohexanone, oxime;n-hydroxycyclohexanimine;cyclohexanone oxime cyc Show more
Specifications & Purity
≥97%
Names and Identifiers Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488180469
Canonical Smiles
C1CCC(=NO)CC1
IUPAC Name
N-cyclohexylidenehydroxylamine
InChIKey
VEZUQRBDRNJBJY-UHFFFAOYSA-N
INCHI
1S/C6H11NO/c8-7-6-4-2-1-3-5-6/h8H,1-5H2
Isomeric SMILES
C1CCC(=NO)CC1
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1209600&ln=
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic nitrogen compounds Class Organonitrogen compounds Subclass Oximes Intermediate Tree Nodes Not available Direct Parent Ketoximes Alternative Parents Organopnictogen compounds Organic oxygen compounds Hydrocarbon derivatives Molecular Framework Aliphatic homomonocyclic compounds Substituents Ketoxime - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aliphatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as ketoximes. These are organic compounds with the general formula RC(R')=NOH (R,R' = organyl). 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 Soluble in water; Soluble in Ether,Alcohol Flash Point(°F) 217°F Flash Point(°C) 103°C Boil Point(°C) 210 °C Melt Point(°C) 90°C Molecular Weight 113.160 g/mol XLogP3 1.200 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 0 Exact Mass 113.084 Da Monoisotopic Mass 113.084 Da Topological Polar Surface Area 32.600 Ų Heavy Atom Count 8 Formal Charge 0 Complexity 90.700 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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