What is the 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE?

3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is , while it's Molecular Formula is C6H8 O2. Used in Food and Beverage Industry: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is used as a flavoring substance for its aromatic properties, enhancing the taste and aroma of various food and beverage products. Used in Fragrance and Perfume Industry: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is used as a key ingredient in the production of fragrances and perfumes, contributing to their unique and appealing scents. Used in Cosmetics Industry: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is utilized in the formulation of cosmetics due to its aromatic properties, adding a pleasant scent and enhancing the sensory experience of the products. Used in Pharmaceutical Industry: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE has potential applications in the pharmaceutical field, serving as an intermediate for the synthesis of other organic compounds with therapeutic properties. Used in Chemical Research: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is employed in chemical research for its unique chemical structure and potential to contribute to the development of new compounds and materials.

What is the CAS number for 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE?

The CAS number of 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is 5870-63-3.

What is 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE (5870-63-3) used for?

3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE, also known as 3-Methyl-3-hydroxy-cyclopent-2-en-1-one, is a chemical compound characterized by the molecular formula C6H8O2. It is a pale yellow liquid that exhibits a floral, herbal, and sweet odor, making it a versatile ingredient in various industries.

What is the 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE?

3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is , while it's Molecular Formula is C6H8 O2. Used in Food and Beverage Industry: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is used as a flavoring substance for its aromatic properties, enhancing the taste and aroma of various food and beverage products. Used in Fragrance and Perfume Industry: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is used as a key ingredient in the production of fragrances and perfumes, contributing to their unique and appealing scents. Used in Cosmetics Industry: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is utilized in the formulation of cosmetics due to its aromatic properties, adding a pleasant scent and enhancing the sensory experience of the products. Used in Pharmaceutical Industry: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE has potential applications in the pharmaceutical field, serving as an intermediate for the synthesis of other organic compounds with therapeutic properties. Used in Chemical Research: 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is employed in chemical research for its unique chemical structure and potential to contribute to the development of new compounds and materials.

What is the CAS number for 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE?

The CAS number of 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE is 5870-63-3.

What is 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE (5870-63-3) used for?

3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE, also known as 3-Methyl-3-hydroxy-cyclopent-2-en-1-one, is a chemical compound characterized by the molecular formula C6H8O2. It is a pale yellow liquid that exhibits a floral, herbal, and sweet odor, making it a versatile ingredient in various industries.

Reputable factory supply 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE 5870-63-3 in stock with high standard

3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE

CAS No.: 5870-63-3
Purity: 99%

Reputable factory supply 3-HYDROXY-2-METHYL-CYCLOPENT-2-ENONE 5870-63-3 in stock with high standard

Molecular Formula: C6H8 O2
Molecular Weight: 112.128
Melting Point: 213-215 °C(Solv: ethanol (64-17-5))
Boiling Point: 212.2°Cat760mmHg
PKA: 4.82±0.30(Predicted)
Flash Point: 84.4°C
PSA： 37.30000
Density: 1.225g/cm³
LogP: 1.18130

5870-63-3 Relevant articles

Conversion of cycloalk-2-enones into 2-methylcycloalkane-1,3-diones - Assessment of various Tamao-Fleming procedures and mechanistic insight into the use of the Me3SiMe2Si unit

Yu, Guojun,Clive, Derrick L. J.

, p. 1653 - 1664 (2016/02/10)

Conjugate addition of Me3SiMe2SiLi to cy...

Reactions of 1,2-bis(trimethylsilyloxy)cycloalkenes with the diethyl acetals of aldehydes

Gao, Fuye,Burnell, D. Jean

, p. 356 - 359 (2007/10/03)

Lewis acid-mediated reactions of 1,2-bis...

5870-63-3 Process route

: 54972-03-1
2-methylcyclopentane-1,3-dione ethylene glycol monoacetal

: 5870-63-3
3-hydroxy-2-methyl-2-cyclopenten-1-one

Conditions

Conditions	Yield
With hydrogenchloride; In tetrahydrofuran; water; for 10h;	71%

: 930-30-3
cyclopent-2-enone

: 5870-63-3
3-hydroxy-2-methyl-2-cyclopenten-1-one

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1.1: N,N,N,N,N,N-hexamethylphosphoric triamide; methyllithium / diethyl ether / 0.5 h / 0 °C / Inert atmosphere 1.2: 1 h / -78 °C / Inert atmosphere 1.3: 3 h / -78 - 20 °C / Inert atmosphere 2.1: toluene-4-sulfonic acid / benzene / 6 h / Reflux; Dean-Stark 3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.33 h / Inert atmosphere 3.2: 20 h 4.1: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / dichloromethane / 0.5 h / Molecular sieve; Inert atmosphere 5.1: hydrogenchloride / tetrahydrofuran; water / 10 h With hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; tetrapropylammonium perruthennate; tetrabutyl ammonium fluoride; methyllithium; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; In tetrahydrofuran; diethyl ether; dichloromethane; water; benzene; 3.2: \|Tamao-Kumada Oxidation;

Yield

Multi-step reaction with 5 steps

1.1: N,N,N,N,N,N-hexamethylphosphoric triamide; methyllithium / diethyl ether / 0.5 h / 0 °C / Inert atmosphere

1.2: 1 h / -78 °C / Inert atmosphere

1.3: 3 h / -78 - 20 °C / Inert atmosphere

2.1: toluene-4-sulfonic acid / benzene / 6 h / Reflux; Dean-Stark

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.33 h / Inert atmosphere

3.2: 20 h

4.1: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / dichloromethane / 0.5 h / Molecular sieve; Inert atmosphere

5.1: hydrogenchloride / tetrahydrofuran; water / 10 h

With hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; tetrapropylammonium perruthennate; tetrabutyl ammonium fluoride; methyllithium; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; In tetrahydrofuran; diethyl ether; dichloromethane; water; benzene; 3.2: |Tamao-Kumada Oxidation;