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

CAS: 3637-61-4 Cat. No.: C121238 Summenformel: C₆H₁₂O Molekulargewicht: 100.16 Beilstein Registry Number: 1919000 EG-Nummer: 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

Room temperature,Argon charged

Shipped In

Normal

Übersicht

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

Synonyme

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 |

Spezifikationen & Reinheit

≥98%

Storage

Room temperature,Argon charged

Verschickt in

Normal

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

488185384

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488185384

Kanonisches Lächeln

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

Isomere SMILES

C1CCC(C1)CO

WGK Deutschland

3

Molekulargewicht

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
    • Klasse Organooxygen compounds
      • Subclass Alcohols and polyols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Air sensitive
• Brechungsindex: 1.458
• Flammpunkt (°F): 143.6 °F
• Flammpunkt (°C): 62°C
• Siedepunkt (°C): 162-163°C
• Molekulargewicht: 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