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2-(4-isobutylphenyl)propionaldehyde

CAS No.
51407-46-6
Chemical Name:
2-(4-isobutylphenyl)propionaldehyde
Synonyms
Ibuprofen Aldehyde;Ibuprofen Impurity 75;2-(4-Isobutylphenyl)propanal;2-(4-isobutylphenyl)propionaldehyde;p-(2-Methylpropyl)hydratropaldehyde;2-[4-(2-Methylpropyl)phenyl]propanal;α-Methyl-4-isobutylbenzeneacetaldehyde;(2RS)-2-[4-(2-Methylpropyl)phenyl]propan-1-al;A-METHYL-4-(2-METHYLPROPYL)BENZENEACETALDEHYDE;α-Methyl-4-(2-methylpropyl)benzeneacetaldehyde
CBNumber:
CB1902754
Molecular Formula:
C13H18O
Molecular Weight:
190.28
MDL Number:
MFCD01940896
MOL File:
51407-46-6.mol
MSDS File:
SDS
Last updated:2023-10-21 13:33:47

2-(4-isobutylphenyl)propionaldehyde Properties

Boiling point 64-65 °C(Press: 0.2 Torr)
Density 0.937±0.06 g/cm3(Predicted)
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility Chloroform (Slightly), Methanol (Slightly)
form Oil
color Colourless
Stability Hygroscopic
FDA UNII ALC8A4Q82T

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H319-H315
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501

2-(4-isobutylphenyl)propionaldehyde price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC I780360 2-(4-Isobutylphenyl)propanal 51407-46-6 25mg $310 2021-12-16 Buy
American Custom Chemicals Corporation CHM0308024 2-(4-ISOBUTYLPHENYL)PROPIONALDEHYDE 95.00% 51407-46-6 5MG $502.52 2021-12-16 Buy
Product number Packaging Price Buy
I780360 25mg $310 Buy
CHM0308024 5MG $502.52 Buy

2-(4-isobutylphenyl)propionaldehyde Chemical Properties,Uses,Production

Uses

2-(4-Isobutylphenyl)propanal is an impurity of the drug Ibuprofen (I140000), a selective cyclooxygenase inhibitor that also inhibits PGH synthase-1 and PGH synthase-2 with comparable potency.

Production Methods

Numerous methods are known for the synthesis of 2-(4-isobutylphenyl)propionaldehyde. It can be prepared by reaction of p-isobutylacetophenone with methyl chloroacetate using sodium methoxide as catalyst, followed by reaction of the glycidic ester with BF3 to give 2- hydroxy-3-(4-isobutylphenyl)-3-butenoic acid methyl ester, which is subsequently treated with mineral acid Avariant of the process is the hydrolysis of the intermediately formed glycidic ester with alkali to give the corresponding salt of glycidic acid, which is then decarboxylated. In addition, 2-(4-isobutylphenyl)propanal is formed by isomerization of 2-(4-isobutylphenyl)- 2-methyloxirane on Al2O3-SiO2 or anhydrous ZnCl2, by reaction of 1-(4-isobutylphenyl)- 1-chloroethane with dimethylformamide in the presence of Li or Na in tetrahydrofuran, and in good yields by Rh- or Co-catalyzed hydroformylation of p-isobutylstyrene.
2-(4-isobutylphenyl)propionaldehyde

2-(4-isobutylphenyl)propionaldehyde Preparation Products And Raw materials

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A-METHYL-4-(2-METHYLPROPYL)BENZENEACETALDEHYDE 2-(4-Isobutylphenyl)propanal 2-[4-(2-Methylpropyl)phenyl]propanal p-(2-Methylpropyl)hydratropaldehyde α-Methyl-4-isobutylbenzeneacetaldehyde alpha-Methyl-4-(2-Methylpropyl)benzeneacetaldehyde 2-(4-isobutylphenyl)propionaldehyde α-Methyl-4-(2-methylpropyl)benzeneacetaldehyde Ibuprofen Aldehyde Benzeneacetaldehyde, α-methyl-4-(2-methylpropyl)- Ibuprofen Impurity 75 (2RS)-2-[4-(2-Methylpropyl)phenyl]propan-1-al 51407-46-6