Cyclohexanone-2,2,6,6-d₄ - ≥98 atom% D,≥98% , CAS No.1006-03-7

CAS: 1006-03-7 Cat. No.: C471914 Fórmula: C₆H₆D₄O Peso molecular: 102.17 Número CE: 686-038-4

GRADE & PURITY ≥98 atom% D,≥98%

Synonyms

Cyclohexanone-2,2,6,6-d4, 98 atom % D | 2,2,6,6-tetradeuteriocyclohexan-1-one | (2,2,6,6-~2~H_4_)Cyclohexanone | Cyclohexanone-2,2,6,6-d4 | (2,2,6,6-?H?)cyclohexan-1-one | D98108 | A935350 | AKOS015912833 | DTXSID20514639 | 2,2,6,6-tetradeuterocyclohexano

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinónimos

Cyclohexanone-2,2,6,6-d4, 98 atom % D | 2,2,6,6-tetradeuteriocyclohexan-1-one | (2,2,6,6-~2~H_4_)Cyclohexanone | Cyclohexanone-2,2,6,6-d4 | (2,2,6,6-?H?)cyclohexan-1-one | D98108 | A935350 | AKOS015912833 | DTXSID20514639 | 2,2,6,6-tetradeuterocyclohexano

Especificações e pureza

≥98 atom% D,≥98%

Condições de armazenamento de armazenamento

Protected from light,Room temperature,Argon charged

Enviado em

Normal

Pureza

≥98 atom% D,≥98%

Nomes e identificadores

• Pubchem Sid: 488198325
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488198325
• Sorrisos canónicos: C1CCC(=O)CC1
• IUPAC Name: 2,2,6,6-tetradeuteriocyclohexan-1-one
• InChIKey: JHIVVAPYMSGYDF-CQOLUAMGSA-N
• INCHI: 1S/C6H10O/c7-6-4-2-1-3-5-6/h1-5H2/i4D2,5D2
• SMILES isoméricas: [2H]C1(CCCC(C1=O)([2H])[2H])[2H]
• Número UN: 1915
• Grupo de embalagem: III
• Peso molecular: 102.17
• Reaxy-Rn: 385735
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=385735&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbonyl compounds
        • Level5 Ketones
          • Level6 Cyclic ketones

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Ketones
• Direct Parent: Cyclic ketones
• Alternative Parents: Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Cyclic ketone - Organic oxide - Hydrocarbon derivative - Aliphatic homomonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as cyclic ketones. These are organic compounds containing a ketone that is conjugated to a cyclic moiety.
• 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

Propriedades químicas e físicas

• Sensibilidade: Moisture sensitive；Light sensitive
• Índice de refração: n20D1.45 (lit.)
• Ponto de ebulição (°C): 153° C (lit.)
• Ponto de fusão (°C): -47° C (lit.)
• Peso molecular: 102.170 g/mol
• XLogP3: 0.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 102.098 Da
• Monoisotopic Mass: 102.098 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 68.200
• Isotope Atom Count: 4
• 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

Referências

1. Liu Xiang, Zhu Yu-Quan, Li Jing, Wang Ye, Shi Qiujin, Li An-Zhen, Ji Kaiyue, Wang Xi, Zhao Xikang, Zheng Jinyu, Duan Haohong.  (2024)  Electrosynthesis of adipic acid with high faradaic efficiency within a wide potential window.  Nature Communications,  15  (1): (1-16).  [PMID:39227577] [10.1038/s41467-024-51951-0]