ChemicalBook--->CAS DataBase List--->4395-92-0

4395-92-0

4395-92-0 Structure

4395-92-0 Structure
IdentificationBack Directory
[Name]

4-isopropylphenylacetaldehyde
[CAS]

4395-92-0
[Synonyms]

CORTEXAL
CUMINICACETALDEHYDE
p-Cymene-7-carboxyaldehyde
ISOPROPYLPHENYLACETALDEHYDE
4-Isopropylphenylacetaldehyd
4-isopropylphenylacetaldehyde
2-(4-propan-2-ylphenyl)ethanal
P-ISOPROPYL PHENYLACETALDEHYDE
PARA-ISOPROPYLPHENYLACETALDEHYDE
2-(4-isopropylphenyl)acetaldehyde
2-(4-propan-2-ylphenyl)acetaldehyde
2-[4-(1-methylethyl)phenyl]-ethanal
4-(1-Methylethyl)benzeneacetaldehyde
Benzeneacetaldehyde, 4-(1-methylethyl)-
Benzeneacetaldehyde, 4-(1-methylethyl)- (9CI)
[EINECS(EC#)]

224-522-5
[Molecular Formula]

C11H14O
[MDL Number]

MFCD00217008
[MOL File]

4395-92-0.mol
[Molecular Weight]

162.23
Chemical PropertiesBack Directory
[Boiling point ]

248.94°C (rough estimate)
[density ]

0.9411 (rough estimate)
[FEMA ]

2954 | P-ISOPROPYL PHENYLACETALDEHYDE
[refractive index ]

1.5400 (estimate)
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[form ]

solid
[Odor]

at 10.00 % in dipropylene glycol. earthy fern aldehydic cumin green cortex
[Odor Type]

green
[JECFA Number]

1024
[Cosmetics Ingredients Functions]

PERFUMING
[InChI]

1S/C11H14O/c1-9(2)11-5-3-10(4-6-11)7-8-12/h3-6,8-9H,7H2,1-2H3
[InChIKey]

FSKGFRBHGXIDSA-UHFFFAOYSA-N
[SMILES]

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

3.12
[EPA Substance Registry System]

Benzeneacetaldehyde, 4-(1-methylethyl)- (4395-92-0)
Safety DataBack Directory
[WGK Germany ]

WGK 2
[TSCA ]

TSCA listed
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Description]

p-Isopropylphenylacetaldehyde has a characteristic bark odor and a citrus, bittersweet, fruity flavor. May be synthesized from cumyl magnesium chloride and ethyl formate or triethyl s-formate followed by acid hydrolysis of the acetal.
[Chemical Properties]

p-Isopropylphenylacetaldehyde has a characteristic bark odor and a citrus, bittersweet, fruity flavor.
[Preparation]

From cumyl magnesium chloride and ethyl formate or triethyl σ-formate followed by acid hydrolysis of the acetal.
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