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

CAS: 3637-61-4 Cat. No.: C121238 Formula: C₆H₁₂O Peso molecolare: 100.16 Beilstein Registry Number: 1919000 Numero 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

Room temperature,Argon charged

Shipped In

Normal

Panoramica

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

Sinonimi

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 |

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged

Spedito in

Normal

Purezza

≥98%

Nomi e identificatori

Pubchem Sid

488185384

Pubchem Sid Url

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

Sorrisi canonici

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

Isomeri SMILES

C1CCC(C1)CO

WGK Germania

3

Peso molecolare

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
    • Classe Organooxygen compounds
      • Subclass Alcohols and polyols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: 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
• Descrizione: 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

Proprietà chimiche e fisiche

• Sensibilità: Air sensitive
• Indice di rifrazione: 1.458
• Punto di infiammabilità (°F): 143.6 °F
• Punto di infiammabilità (°C): 62°C
• Punto di ebollizione (°C): 162-163°C
• Peso molecolare: 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