Ethyl 4-Oxocyclohexanecarboxylate - ≥98%(GC) , CAS No.17159-79-4

CAS: 17159-79-4 Cat. No.: E156205 Formule: C₉H₁₄O₃ Poids moléculaire: 170.21 Beilstein Registry Number: 2520500 Numéro CE: 628-731-6

QUALITÉ & PURETÉ ≥98%(GC)

Synonyms

2-deoxy-2-((18)F)fluoro-alpha-D-glucopyranose|4-ethoxycarbonylcyclohexanone|4-ethoxycarbonyl-cyclohexanone|syn-3-[18F]FACBC|Ethyl 4-oxocyclohexane carboxylate|4-(Ethoxycarbonyl)-1-cyclohexanone|4-carboethoxycyclohexanone|4-carboethoxy-cyclohexanone|4-ethoxycarbonyl cyclohexanone|4-ketocyclohexanecarboxylic acid ethyl ester|ethyl-4-oxo-1-cyclohexane carboxylate|4-carbethoxycyclohexanone|ethyl 4-oxo-cyclohexanoate|4-oxocyclohexane-1-carboxylic acid ethyl ester|4-(Ethoxycarbonyl)cyclohexanone, Ethyl cyclohexanone-4-carboxylate|Ethyl 4-ketocyclohexanecarboxylate|ethyl cyclohexan-4-onecarboxylate|Ethyl cyclohexanone-4-carboxylate|ethyl-4-oxocyclohexanecarboxylate|4-cyclohexanone carboxylic acid ethyl ester|ethyl 4-oxocyclohexane-1-carboxylate|4-OXOCYCLOHEXANECARBOXYLIC ACID, ETHYL ESTER|Ethyl 4-oxocyclohexanecarboxylate|ethyl 4-oxo-cyclohexanecarboxylate|ethyl 4-oxo-cyclo-hexanecarboxylate|ethyl 4-oxocyclohexane-carboxylate|ethyl 4-oxocyclohexanecarbox-ylate|4-oxocyclohexane carboxylic acid ethyl ester|4-oxo-cyclohexane carboxylic acid ethyl ester|Cyclohexanecarboxylic acid, 4-oxo-, ethyl ester|Ethyl 4-Cyclohexanonecarboxylate|ethyl-4-oxocyclohexane carboxylate|4-(Ethoxycarbonyl)cyclohexanone|ethyl 4-oxocyclohexan-1-carboxylate|ethyl 4-oxo-cyclohexylcarboxylate|4-oxocyclohexanecarboxylic acid ethyl ester|4-oxo-cyclohexanecarboxylic acid ethyl ester|4-oxo-cyclo-hexanecarboxylic acid ethyl ester

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble

Employed in the preparation of dopamine agonists and the skeleton of tetracyclic diterpenes

Spécifications

Synonymes

2-deoxy-2-((18)F)fluoro-alpha-D-glucopyranose | 4-ethoxycarbonylcyclohexanone | 4-ethoxycarbonyl-cyclohexanone | syn-3-[18F]FACBC | Ethyl 4-oxocyclohexane carboxylate | 4-(Ethoxycarbonyl)-1-cyclohexanone | 4-carboethoxycyclohexanone | 4-carboethoxy-cyclohexanone | 4-ethoxycarbonyl cyclohexanone | 4-ketocyclohexanecarboxylic acid ethyl est Afficher plus

Spécifications et pureté

≥98%(GC)

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥98%(GC)

Noms et identifiants

Pubchem Sid

488189473

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488189473

Sourires canoniques

CCOC(=O)C1CCC(=O)CC1

IUPAC Name

ethyl 4-oxocyclohexane-1-carboxylate

InChIKey

ZXYAWONOWHSQRU-UHFFFAOYSA-N

INCHI

1S/C9H14O3/c1-2-12-9(11)7-3-5-8(10)6-4-7/h7H,2-6H2,1H3

Isomères SMILES

CCOC(=O)C1CCC(=O)CC1

WGK Allemagne

3

Poids moléculaire

170.21

Beilstein

2520500

Reaxy-Rn

2520501

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2520501&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid esters
• Alternative Parents: Cyclic ketones Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Cyclic ketone - Ketone - Carboxylic acid ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).
• 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.

DOI: 10.1186/s13321-016-0174-y

Propriétés chimiques et physiques

• Indice de réfraction: 1.46
• Point d'éclair (°F): 230 °F
• Point d'éclair (°C): 110 °C
• Point d'ébullition (°C): 152°C/40mmHg(lit.)
• Poids moléculaire: 170.210 g/mol
• XLogP3: 0.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 170.094 Da
• Monoisotopic Mass: 170.094 Da
• Topological Polar Surface Area: 43.400 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 176.000
• 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