3-Methyl-2-cyclopentenone

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Products Intro: Product Name:3-methylcyclopent-2-en-1-one
CAS:2758-18-1
Purity:98% GC Package:25kg|50kg Remarks:3-Methylcyclopent-2-en-1-one 3-Methylcyclopent3-methylcyclopent-2-en-1-one-2-en-1-one, 98%
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CAS:2758-18-1
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CAS:2758-18-1
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Products Intro: Product Name:3-Methyl-2-cyclopenten-1-one
CAS:2758-18-1
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Products Intro: Product Name:3-Methyl-2-cyclopenten-1-one
CAS:2758-18-1
Purity:99% Package:1KG;30.00;USD|10KG;20.00;USD|100KG;10.00;USD

3-Methyl-2-cyclopentenone manufacturers

3-Methyl-2-cyclopentenone Basic information
Product Name:3-Methyl-2-cyclopentenone
Synonyms:3-METHYL-2-CYCLOPENTEN-1-ONE FOR SYNTHES;3-methyl-2-cyclopenten-1-on;3-Methyl-cyclopent-2-enone;3-Methyl-2-cyclopentenone 97%;3-Methyl-2-cyclopenten-1-one, 97%+;3-Methyl-2-cyclopenten-1-one, GC 98%;3-Methyl-2-cyclopenten-1-one, stabilised;3-Methyl-2-cyclopenten-1-one, stabilized, 98% 10GR
CAS:2758-18-1
MF:C6H8O
MW:96.13
EINECS:220-421-5
Product Categories:C3 to C6;Carbonyl Compounds;ketone;Ketones;Building Blocks;C3 to C6;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Pyridines
Mol File:2758-18-1.mol
3-Methyl-2-cyclopentenone Structure
3-Methyl-2-cyclopentenone Chemical Properties
Melting point 3-5 °C (lit.)
Boiling point 74 °C/15 mmHg (lit.)
density 0.980 g/mL at 20 °C 0.971 g/mL at 25 °C (lit.)
FEMA 3435 | 1-METHYL-1-CYCLOPENTEN-3-ONE
refractive index n20/D 1.488(lit.)
Fp 150 °F
storage temp. 2-8°C
solubility Soluble in DMSO
form Liquid
color Clear light yellow to yellow-brown
Odorat 1.00 % in dipropylene glycol. sweet fruity fatty
PH4.9 (10g/l, H2O, 20℃)
Odor Typefruity
biological sourcesynthetic
Water Solubility miscible
JECFA Number1105
BRN 1280476
Major Applicationflavors and fragrances
InChI1S/C6H8O/c1-5-2-3-6(7)4-5/h4H,2-3H2,1H3
InChIKeyCHCCBPDEADMNCI-UHFFFAOYSA-N
SMILESCC1=CC(=O)CC1
LogP0.54
CAS DataBase Reference2758-18-1(CAS DataBase Reference)
NIST Chemistry Reference2-Cyclopenten-1-one, 3-methyl-(2758-18-1)
EPA Substance Registry System3-Methyl-2-cyclopenten-1-one (2758-18-1)
Safety Information
Risk Statements 36/38
Safety Statements 24/25
RIDADR 1224
WGK Germany 3
TSCA TSCA listed
HazardClass CBL
PackingGroup III
HS Code 29142900
Storage Class10 - Combustible liquids
MSDS Information
ProviderLanguage
3-Methyl-2-cyclopenten-1-one English
SigmaAldrich English
ACROS English
ALFA English
3-Methyl-2-cyclopentenone Usage And Synthesis
DescriptionMay be prepared by dehydrohalogenation of 2-chloro-l-methylcyclopentan-3-one.
Chemical Propertiesclear light yellow to yellow-brownish liquid
Chemical Properties1-Methyl-1-cyclopenten-3-one has a sweet-floral, warm-spicy and diffusive yet quite tenacious odor.
OccurrenceReported found in roasted onion, cooked pork, black tea, soybean and dried bonito
Uses3-Methyl-2-cyclopentenone was used in the synthesis of 2-hydroxy-3-methyl-2-cyclopentenone.
UsesIt is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals.
Application 3-Methyl-2-cyclopentenone is used as an important intermediate in the production of various natural products and petrol additives[1].
DefinitionChEBI: 3-Methyl-2-cyclopenten-1-one is a cyclic ketone.
PreparationBy dehydrohalogenation of 2-chloro-1-methyl-cyclopentan-3-one.
Synthesis Reference(s)Journal of the American Chemical Society, 101, p. 494, 1979 DOI: 10.1021/ja00496a044
The Journal of Organic Chemistry, 55, p. 371, 1990
General Description3-Methyl-2-cyclopenten-1-one is a component of smoke flavoring.
Synthesis3-Methyl-2-cyclopentenone (MCP) can be selectively synthesised via 2,5-hexanedione (HD) using a heterogeneous catalyst as a support. In a heterogeneous catalytic system, Bell et al. found that a Mg-Al-Ox catalyst, prepared by calcining MgAl hydrotalcite at 700 °C, achieved both a yield and selectivity of 98% when converting HD to MCP in a formaldehyde/water two-phase medium. In addition, the use of simple alumina-based solid acid catalysts, such as γ-Al?O? and AlOOH, can achieve a selectivity of over 71% in the conversion of HD to MCP[1].
synthesis of 3-Methyl-2-cyclopentenone
References[1] Shun Nishimura, Kohki E., Shintaro Ohmatsu. (2019). Selective synthesis of 3-methyl-2-cyclopentenone via intramolecular aldol condensation of 2,5-hexanedione with γ-Al2O3/AlOOH nanocomposite catalyst. Fuel Processing Technology, 196, Article 106185. https://doi.org/10.1016/j.fuproc.2019.106185
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