58101-60-3

  • Product Name:Methyl 3-cyclopentenecarboxylate
  • Molecular Formula:C7H10O2
  • Purity:98% GC
  • Molecular Weight:126.155
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Product Details

Factory Export Top Purity Methyl 3-cyclopentenecarboxylate 58101-60-3 In Stock

  • Molecular Formula:C7H10O2
  • Molecular Weight:126.155
  • Vapor Pressure:3.95mmHg at 25°C 
  • Refractive Index:1.473 
  • Boiling Point:149.8 ºC at 760 mmHg 
  • Flash Point:33.8 ºC 
  • PSA:26.30000 
  • Density:1.054 g/cm3 
  • LogP:1.12560 

Methyl 3-cyclopentenecarboxylate(Cas 58101-60-3) Usage

Use Description

Methyl 3-cyclopentenecarboxylate is a chemical compound with versatile applications in various fields. In the realm of organic synthesis and chemical research, it serves as a valuable building block for the creation of complex organic molecules and pharmaceutical compounds, facilitating drug discovery and the development of potential therapeutic agents. Additionally, in the fragrance and flavor industry, Methyl 3-cyclopentenecarboxylate can be utilized to impart unique scents and flavors, enhancing the sensory experiences of perfumes, cosmetics, and food products. Its applications in organic synthesis and fragrance creation underscore its significance in driving innovation, scientific exploration, and product development within these distinct domains.

InChI:InChI=1/C7H10O2/c1-9-7(8)6-4-2-3-5-6/h2-3,6H,4-5H2,1H3

58101-60-3 Relevant articles

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Bond,F.T.,Ho,C.-Y.

, p. 1421 - 1425 (1976)

-

A FACILE SYNTHESIS OF (+/-)-SESBANINE VIA γ-ADDITION OF KETENE SILYL ACETAL WITH QUATERNIZED METHYL NICOTINATE

Wada, Makoto,Nishihara, Yoshihiro,Akiba, Kin-ya

, p. 3267 - 3270 (1985)

Total synthesis of (+/-)-sesbanine (1) w...

Synthesis and Conformational Aspects of cis- and trans-3-Carbomethoxy-6-oxabicyclohexane

Lizotte, Kathryn E.,Marecki, Paul E.,Mertes, Mathias P.

, p. 3594 - 3597 (1983)

-

Carbocyclic 3′-deoxyadenosine-based highly potent bisubstrate-analog inhibitor of basophilic protein kinases

Enkvist, Erki,Raidaru, Gerda,Vaasa, Angela,Pehk, T?nis,Lavogina, Darja,Uri, Asko

, p. 5336 - 5339 (2007)

Carbocyclic analogs of 3′-deoxyadenosine...

3-(1H-PYRAZOL-4-YL)PYRIDINE ALLOSTERIC MODULATORS OF THE M4 MUSCARINIC ACETYLCHOLINE RECEPTOR

-

Page/Page column 35, (2019/01/16)

The present invention is directed to pyr...

Copper-Catalyzed Modular Amino Oxygenation of Alkenes: Access to Diverse 1,2-Amino Oxygen-Containing Skeletons

Hemric, Brett N.,Chen, Andy W.,Wang, Qiu

supporting information, p. 1468 - 1488 (2019/01/25)

Copper-catalyzed alkene amino oxygenatio...

Hydroalkylation of Olefins to Form Quaternary Carbons

Green, Samantha A.,Huffman, Tucker R.,McCourt, Ruairí O.,Van Der Puyl, Vincent,Shenvi, Ryan A.

supporting information, (2019/05/22)

Metal-hydride hydrogen atom transfer (MH...

Hydroalkylation of Olefins to Form Quaternary Carbons

Green, Samantha A.,Huffman, Tucker R.,McCourt, Ruairí O.,Van Der Puyl, Vincent,Shenvi, Ryan A.

supporting information, p. 7709 - 7714 (2019/05/22)

Metal-hydride hydrogen atom transfer (MH...

58101-60-3 Process route

methanol
67-56-1

methanol

3-cyclopentene-1-carboxylic acid
7686-77-3

3-cyclopentene-1-carboxylic acid

methyl cyclopent-3-ene-1-carboxylate
58101-60-3

methyl cyclopent-3-ene-1-carboxylate

Conditions
Conditions Yield
3-cyclopentene-1-carboxylic acid; With 1,1'-carbonyldiimidazole; In dichloromethane; at 0 - 20 ℃; for 4h;
methanol; In dichloromethane;
99%
With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide;
85%
With sulfuric acid; at 0 - 80 ℃; for 6h;
80%
With thionyl chloride; at -70 - 0 ℃; for 1h;
65%
With N-(3-dimethylaminopropyl)-N-ethylcarbodiimide;
53%
With sulfuric acid; at 20 ℃; for 16.5h;
3-cyclopentene-1-carboxylic acid
7686-77-3

3-cyclopentene-1-carboxylic acid

methyl iodide
74-88-4

methyl iodide

methyl cyclopent-3-ene-1-carboxylate
58101-60-3

methyl cyclopent-3-ene-1-carboxylate

Conditions
Conditions Yield
With potassium carbonate; In DMF (N,N-dimethyl-formamide); at 20 ℃; for 16h;
96%
With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 16h;
96%
With potassium carbonate; In DMF (N,N-dimethyl-formamide); at 20 ℃; for 16h;
96%
With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 16h; Schlenk technique; Inert atmosphere;
87%
With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 16h;
86%

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