(2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde

Basic Information

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CAS Number

4501-58-0

Molecular Formula

C10H16O

Molecular Weight

152.24 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Aldehydes

Basic Physical Properties

Refractive Index

1.47

SMILES

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CC1=CC[C@H](CC=O)C1(C)C

InChI

InChI=1S/C10H16O/c1-8-4-5-9(6-7-11)10(8,2)3/h4,7,9H,5-6H2,1-3H3/t9-/m1/s1

InChIKey

OGCGGWYLHSJRFY-SECBINFHSA-N

LogP

2.567800000000001

Topological Polar Surface Area

17.07 Å²

Hydrogen Bond Donor/Acceptor

0 / 1

Synonyms & References

English

Campholenic Aldehyde
Trimethyl cyclopentenyl acetaldehyde
Aromavert
2,2,3-trimethyl-1-acetaldehyde-3-cyclopentene
(2,2,3-Trimethyl-cyclopent-3-enyl)-acetaldehyde
C10H16O
(+/-)-2,2,3-trimethyl-cyclopent-3-ene-1-acetaldehyde
(R)-alpha-campholenaldehyde
(R)-Campholenaldehyde
2-(2,2,3-trimethylcyclopent-3-en-1-yl)-acetaldehyde
2-(2,2,3-trimethylcyclopent-3-enyl)acetaldehyde
2,2,3-trimethyl-3-cyclopenten-1-acetaldehyde
Alphaampholenic Aldehyde
CAMPHOLENALDEHYD P
campholene aldehyde
CAMPHOLENIALDEHYDE
2,2,3-Trimethylcyclopent-3-en-1-yl-acetaldehyde

MDL Number

MFCD00274368

Customs Code

2912299000

FAQ

What are the physical and chemical properties of (2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde (CAS: 4501-58-0)?

(2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde is a colorless liquid with a molecular weight of approximately 128.21 g/mol. It has a specific gravity of 0.875 and is slightly soluble in water. It is susceptible to oxidation and has a moderate reactivity. This compound is prone to form peroxides over time, which are potential explosion hazards.

How is (2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde (CAS: 4501-58-0) typically synthesized?

(2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde can be synthesized through the oxidation of the corresponding cyclopentene. Common methods include catalytic oxidation using copper salts or potassium permanganate. The reaction is typically carried out in an acidic medium, and the yield is around 70-80% depending on the reaction conditions.

What industries use (2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde (CAS: 4501-58-0)?

(2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde is used primarily in the pharmaceutical industry for the synthesis of various organic compounds. It also finds applications in the polymer industry as a monomer, in the production of sensors, and as a precursor in semiconductor manufacturing processes.

What precautions should be taken when handling (2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde (CAS: 4501-58-0)?

When handling (2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde, it is essential to wear appropriate personal protective equipment (PPE) such as gloves, safety goggles, and a lab coat. The compound should be stored in a cool, dry area away from oxidizing agents. Spills should be cleaned up using appropriate methods, and the area should be well-ventilated. Always refer to the Safety Data Sheet (SDS) for additional safety information.