Cyclopentanemethanol - ≥98% , CAS No.3637-61-4

CAS: 3637-61-4 Cat. No.: C121238 Peso molecular: 100.16 Beilstein Registry Number: 1919000 Número EC: 222-861-3

GRADE & PURITY ≥98%

Synonyms

W-106621 | AKOS009157998 | DTXSID70189896 | F0001-1040 | UNII-4LG8NG324P | SCHEMBL5625 | cyclopentyl methanol | EN300-49287 | C2658 | D-fructose-6-P | 3,4,5-TRIMETHOXY PHENOL | EINECS 222-861-3 | Malvinidin | Cyclopentanemethanol | cyclo-pentanemethanol |

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

Application

Cyclopentanemethanol was used to study catalytic reduction of 6-bromo-1-hexene by nickel (I) salen electrogenerated at a glassy carbon electrode in acetonitrile containing tetramethylammonium tetrafluoroborate by cyclic voltammetry and controlled-potential electrolysis.

Specifications

Sinónimos

W-106621 | AKOS009157998 | DTXSID70189896 | F0001-1040 | UNII-4LG8NG324P | SCHEMBL5625 | cyclopentyl methanol | EN300-49287 | C2658 | D-fructose-6-P | 3, 4, 5-TRIMETHOXY PHENOL | EINECS 222-861-3 | Malvinidin | Cyclopentanemethanol | cyclo-pentanemethanol |

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488185384
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185384
• Sonrisas canónicas: C1CCC(C1)CO
• IUPAC Name: cyclopentylmethanol
• InChIKey: ISQVBYGGNVVVHB-UHFFFAOYSA-N
• INCHI: 1S/C6H12O/c7-5-6-3-1-2-4-6/h6-7H,1-5H2
• Isómeros SMILES: C1CCC(C1)CO
• WGK Alemania: 3
• Peso molecular: 100.16
• Beilstein: 1919000
• Reaxy-Rn: 1919000
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1919000&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Alcohols and polyols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Alcohols and polyols
• Intermediate Tree Nodes: Not available
• Direct Parent: Primary alcohols
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic homomonocyclic compounds
• Substituents: Hydrocarbon derivative - Primary alcohol - Aliphatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as primary alcohols. These are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl).
• 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

Propiedades químicas y físicas

• Sensibilidad: Air sensitive
• Índice de refracción: 1.458
• Punto de inflamación (°F): 143.6 °F
• Punto de inflamación (°C): 62°C
• Punto de ebullición (°C): 162-163°C
• Peso molecular: 100.160 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 100.089 Da
• Monoisotopic Mass: 100.089 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 46.100
• 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

Referencias

1. Luyao Guo, Xiaoyan Liu, Ziang Zhao, Ronghe Lin, Yu Meng, Xinzheng Ma, Yihui Li, Xiaoling Mou, Li Yan, Hejun Zhu, Yunjie Ding.  (2023)  Nanostructured PtBi Alloy Enables Direct Oxidation of Linear α-Alcohols to Fatty Acids.  ACS Catalysis,      [PMID:] [10.1021/acscatal.3c03458]