Cyclopentanecarboxaldehyde - ≥98%, contains 0.1% hydroquinone as stabilizer , CAS No.872-53-7

CAS: 872-53-7 Cat. No.: C122650 Summenformel: C₅H₉CHO Molekulargewicht: 98.14 EG-Nummer: 212-829-7

GRADE & PURITY ≥98%, contains 0.1% hydroquinone as stabilizer

Synonyms

Cyclopentanecarbaldehyde, 0.1% hydroquinone as stabilizer | cyclopentanecaboxaldehyde | C3019 | Formylcyclopentane | Cyclopentanecarbaldehyde | EN300-57255 | Cyclopentanecarboxaldehyde (25ppm 1,4-Benzoquinone as stabiliser) | BBL100156 | Cyclopentanealdeh

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Übersicht

Cyclopentanecarboxaldehyde can be prepared from cyclohexene, via copper-catalyzed oxidation with persulfate. It can also be synthesized from mercuric sulfate and cyclohexene.

Cyclopentanecarboxaldehyde may be used in the synthesis of:

· D,L-trans-2-cyclopentylmethylene-1-nitroso-1-(2-hydroxycyclohexyl)hydrazine

· ethyl 5-cyclopentyl-5-hydroxy-2-pentenoate

· ethyl 3-cyclo entyl-3-hydroxy-2-vinylpropanoate

Specifications

Synonyme

Cyclopentanecarbaldehyde, 0.1% hydroquinone as stabilizer | cyclopentanecaboxaldehyde | C3019 | Formylcyclopentane | Cyclopentanecarbaldehyde | EN300-57255 | Cyclopentanecarboxaldehyde (25ppm 1,4-Benzoquinone as stabiliser) | BBL100156 | Cyclopentanealdeh

Spezifikationen & Reinheit

≥98%, contains 0.1% hydroquinone as stabilizer

Storage

Store at 2-8°C,Argon charged

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥98%

Namen und Kennungen

• Pubchem Sid: 508814744
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508814744
• Kanonisches Lächeln: C1CCC(C1)C=O
• IUPAC Name: cyclopentanecarbaldehyde
• InChIKey: VELDYOPRLMJFIK-UHFFFAOYSA-N
• INCHI: 1S/C6H10O/c7-5-6-3-1-2-4-6/h5-6H,1-4H2
• Isomere SMILES: C1CCC(C1)C=O
• WGK Deutschland: 3
• UN-Nummer: 1989
• Molekulargewicht: 98.14
• Reaxy-Rn: 1560515
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1560515&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organic oxides

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organic oxides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic oxides
• Alternative Parents: Hydrocarbon derivatives Aldehydes
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - Aliphatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as organic oxides. These are organic compounds containing an oxide 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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in water and ethanol
• Empfindlichkeit: Heat sensitive; Air sensitive
• Brechungsindex: 1.443
• Flammpunkt (°F): 82.4 °F
• Flammpunkt (°C): 28 °C
• Siedepunkt (°C): 140-141°C
• Molekulargewicht: 98.140 g/mol
• XLogP3: 1.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 98.0732 Da
• Monoisotopic Mass: 98.0732 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 62.600
• 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

Referenzen

1. Jing Zhang, Xun Kuang, Linyu Zhu, Xintong Xiao, Zhongyue Zhou, Fei Qi.  (2024)  Sustainable production of cyclohexanones through hydrodeoxygenation of lignin-derived phenolics over PdFe/HZSM-5 catalysts.  FUEL,      [PMID:] [10.1016/j.fuel.2024.133863]

2. Yingxuan Zhao, Chenyang Shen, Qing Liu, Siyuan Zhao, Ruiyao Zhao, Xiangke Guo, Nianhua Xue, Luming Peng, Xuefeng Guo, Yan Zhu, Weiping Ding.  (2026)  Electrocatalytic oxidation or amidation of olefins by asymmetric electrolytes steering carbocation pathways.  GREEN CHEMISTRY,      [PMID:] [10.1039/D5GC07050C]