1462-96-0

  • Product Name1-Ethylcyclopentanol
  • Molecular FormulaC7H14O
  • Molecular Weight114.19
  • Purity99%
  • AppearanceLight yellow liquid
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Product Details

Quick Details

  • CasNo: 1462-96-0
  • Molecular Formula: C7H14O
  • Appearance: Light yellow liquid
  • Purity: 99%

High Purity 1-Ethylcyclopentanol 1462-96-0 Liquid

  • Molecular Formula:C7H14O
  • Molecular Weight:114.188
  • Appearance/Colour:Light yellow liquid 
  • Vapor Pressure:0.73mmHg at 25°C 
  • Melting Point:-10°C(lit.) 
  • Refractive Index:1.463 
  • Boiling Point:154 °C at 760 mmHg 
  • PKA:15.38±0.20(Predicted) 
  • Flash Point:56.2 °C 
  • PSA:20.23000 
  • Density:0.938 g/cm3 
  • LogP:1.70150 

1462-96-0 Usage

1-Ethylcyclopentanol (1-ECP) is a cyclic alcohol that is widely used in the synthesis of organic compounds.

Isomeric SMILES: CCC1(CCCC1)O  
InChIKey: LPCWIFPJLFCXRS-UHFFFAOYSA-N  
InChI: InChI=1S/C7H14O/c1-2-7(8)5-3-4-6-7/h8H,2-6H2,1H3  

1462-96-0 Relevant articles

Oxidative cleavage of tertiary cyclic alcohols by Pb(OAc)4-KSCN system

S. S. Spektor, N. I. Kapustina, E. P. Kaplan & G. I. Nikishin

Bulletin of the Academy of Sciences of the USSR, Division of chemical science volume 28, pages1066–1068 (1979)

Oxidation of 1-Ethylcyclopentanol with LTA. A mixture of 0.01 mole of 1-ethylcyclopentanol, … We obtained 9 mmoles of 1-ethylcyclopentanol and 0.5 mmole of ethyl butyl ketone. Infrared …

Carbon Dioxide as a Directing Group for C-H Functionalization Reactions Involving Lewis Basic Amines, Alcohols, Thiols, and Phosphines for the Synthesis of Compounds

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Paragraph 0092-0094; 0100, (2019/07/03)

Methods of synthesizing compounds using CO2 as a directing group for C—H functionalization, and compounds made thereby, are described.

Diester acid protection structure monomer and preparation method thereof

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Paragraph 0086-0092, (2020/01/03)

The invention relates to the field of optical materials and in particular to a diester acid protection structure monomer and a preparation method thereof. Due to a diester long side chain, the photoresist has a better film-forming property; due to the fact that small-size and high-acid-sensitivity groups hung outside can improve the deprotection reaction efficiency in the photoetching process, the quality of a photoetched product is improved; and in addition, the diester acid protection structure monomer prepared through the process method has high yield and purity, and the performance of the photoresist is further guaranteed.

Transaminase Triggered Aza-Michael Approach for the Enantioselective Synthesis of Piperidine Scaffolds

Ryan, James,?iau?iulis, Mindaugas,Gomm, Andrew,Maciá, Beatriz,O’Reilly, Elaine,Caprio, Vittorio

supporting information, p. 15798 - 15800 (2016/12/22)

The expanding “toolbox” of biocatalysts opens new opportunities to redesign synthetic strategies to target molecules by incorporating a key enzymatic step into the synthesis. Significantly, we show that the reversible enzymatic process can power the shuttling of amine functionality across a molecular framework, providing access to the desired aza-Michael products.

1462-96-0 Process route

1-cyclopentylethan-1-amine
38118-79-5,150852-72-5

1-cyclopentylethan-1-amine

cis-nitrous acid
7782-77-6

cis-nitrous acid

1-ethylcyclopentanol
1462-96-0

1-ethylcyclopentanol

1-cyclopentylethan-1-ol
52829-98-8

1-cyclopentylethan-1-ol

(+/-)-trans-2-methylcyclohexanol
7443-52-9

(+/-)-trans-2-methylcyclohexanol

Conditions
Conditions Yield
 
 
1-ethynylcyclopentanol
17356-19-3

1-ethynylcyclopentanol

1-ethylcyclopentanol
1462-96-0

1-ethylcyclopentanol

Conditions
Conditions Yield
With magnesium; palladium on activated charcoal; In methanol; Ambient temperature;
90%
With 5%-palladium/activated carbon; hydrogen; In methanol; at 80 ℃; under 22502.3 Torr; Autoclave;
 

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