3400-45-1

  • Product Name:Cyclopentanecarboxylic acid
  • Molecular Formula:C6H10O2
  • Purity:99%
  • Molecular Weight:114.144
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Product Details

Factory Sells Best Quality Cyclopentanecarboxylic acid 3400-45-1 with steady supply

  • Molecular Formula:C6H10O2
  • Molecular Weight:114.144
  • Appearance/Colour:clear colorless to yellow liquid 
  • Vapor Pressure:0.0626mmHg at 25°C 
  • Melting Point:3-5 °C(lit.) 
  • Refractive Index:n20/D 1.453(lit.)  
  • Boiling Point:213.832 °C at 760 mmHg 
  • PKA:4.99(at 25℃) 
  • Flash Point:96.251 °C 
  • PSA:37.30000 
  • Density:1.13 g/cm3 
  • LogP:1.26120 

Cyclopentanecarboxylic acid(Cas 3400-45-1) Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 37, p. 3381, 1972 DOI: 10.1021/jo00986a054Synthetic Communications, 20, p. 1353, 1990 DOI: 10.1080/00397919008052848

Purification Methods

If it is discoloured shake it with saturated aqueous NaCl, extract it with Et2O, dry the extract (MgSO4), filter, evaporate and distil the residue preferably under a vacuum. The lachrymatory acid chloride has M 114.1, m 4o and b 216o/atm, d4 1.091, nD 1.4620. [Beilstein 9 H 6, 9 IV 11.]

InChI:InChI=1/C6H10O2/c7-6(8)5-3-1-2-4-5/h5H,1-4H2,(H,7,8)/p-1

3400-45-1 Relevant articles

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Edwards,Lesage

, p. 2071 (1959)

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Loftfield

, p. 632 (1950)

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Transformation of Thioacids into Carboxylic Acids via a Visible-Light-Promoted Atomic Substitution Process

Fu, Qiang,Liang, Fu-Shun,Lou, Da-Wei,Pan, Gao-Feng,Wang, Rui,Wu, Min,Xie, Kai-Jun

supporting information, p. 2020 - 2024 (2022/03/31)

A visible-light-promoted atomic substitu...

Gram-scale synthesis of carboxylic acids via catalytic acceptorless dehydrogenative coupling of alcohols and hydroxides at an ultralow Ru loading

Chen, Cheng,Cheng, Hua,Verpoort, Francis,Wang, Zhi-Qin,Wu, Zhe,Yuan, Ye,Zheng, Zhong-Hui

, (2021/12/13)

Acceptorless dehydrogenative coupling (A...

Time-Dependent Self-Assembly of Copper(II) Coordination Polymers and Tetranuclear Rings: Catalysts for Oxidative Functionalization of Saturated Hydrocarbons

Costa, Ines F. M.,Kirillova, Marina V.,André, Vania,Fernandes, Tiago A.,Kirillov, Alexander M.

supporting information, p. 14491 - 14503 (2021/07/19)

This study describes a time-dependent se...

Mild oxidative functionalization of cycloalkanes catalyzed by novel dicopper(II) cores

Trusau, Kiryl I.,Kirillova, Marina V.,André, Vania,Usevich, Andrew I.,Kirillov, Alexander M.

, (2021/02/09)

The search for new transition metal base...

3400-45-1 Process route

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cyclohexanone

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cyclopentanecarboxylic acid

cyclohexane-1,2-dione
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cyclohexane-1,2-dione

cyclohexanone-2-ol
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cyclohexanone-2-ol

Conditions
Conditions Yield
With manganese(IV) oxide; perchloric acid; tris(2,2’-bipyridine)ruthenium(II); for 0.333333h; Product distribution; Thermodynamic data; Rate constant; in prsence and absence of air; ΔH(act.), ΔG(act.), ΔS(act.);
cyclohexanone
108-94-1,11119-77-0,9003-41-2,9075-99-4

cyclohexanone

hexahydro-2H-oxepin-2-one
502-44-3,24980-41-4,80137-66-2

hexahydro-2H-oxepin-2-one

Adipic acid
124-04-9

Adipic acid

6-Hydroxyhexanoic acid
1191-25-9

6-Hydroxyhexanoic acid

cyclopentanecarboxylic acid
3400-45-1

cyclopentanecarboxylic acid

Conditions
Conditions Yield
With tert.-butylhydroperoxide; 2-methyl-1,3,2-benzothiaselenazole 1,1-dioxide; In tert-butyl alcohol; at 65 ℃; for 15h; Further Variations:; Reagents; Product distribution;

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