CAS 13372-80-0

4-(1-Methylethyl)benzaldehyde oxime

Description:

4-(1-Methylethyl)benzaldehyde oxime, also known by its CAS number 13372-80-0, is an organic compound characterized by the presence of both an aromatic ring and an oxime functional group. This compound features a benzaldehyde moiety substituted with an isopropyl group at the para position relative to the aldehyde. The oxime functional group, which is derived from the reaction of the aldehyde with hydroxylamine, imparts unique reactivity and properties to the molecule. Typically, oximes exhibit moderate polarity due to the presence of the hydroxyl and nitrogen functionalities, which can engage in hydrogen bonding. This compound may be utilized in various chemical syntheses and applications, including as an intermediate in the production of pharmaceuticals or agrochemicals. Its physical properties, such as boiling point, melting point, and solubility, can vary based on the specific conditions and purity of the sample. Safety data should be consulted to ensure proper handling, as with all chemical substances.

Formula: C₁₀H₁₃NO

InChI: InChI=1S/C10H13NO/c1-8(2)10-5-3-9(4-6-10)7-11-12/h3-8,12H,1-2H3

InChI key: InChIKey=NVKXBDITZDURNJ-UHFFFAOYSA-N

SMILES: C(C)(C)C1=CC=C(C=NO)C=C1

Synonyms:

• 4-(1-Methylethyl)Benzaldehyde Oxime
• 4-Isopropylbenzaldehyde oxime
• 4-Isopropylbenzaldoxime
• Ai3-07311
• Benzaldehyde, 4-(1-methylethyl)-, oxime
• Benzaldehyde, p-isopropyl-, oxime
• Cuminaldoxime
• NSC 69956

N-{[4-(Propan-2-yl)phenyl]methylidene}hydroxylamine

CAS: 13372-80-0

N-{[4-(Propan-2-yl)phenyl]methylidene}hydroxylamine is a tartrate reagent that is used in the asymmetric synthesis of chiral compounds. It has been shown to be effective in the synthesis of enantiomerically pure amines, ketones, and alcohols. This reagent has been shown to catalyze reactions with high enantioselectivities and tolerates a wide range of functional groups. The tartrate anion is formed stoichiometrically by the reaction of two equivalents of tartaric acid with one equivalent of a base such as dicyclohexyl or dimethylzinc. The glyoxal group may be converted to a dioxane by heating with ethylene glycol at 160 °C for 30 minutes. The acid ester may be hydrolyzed by heating with water at 100 °C for 2 hours.

Formula: C₁₀H₁₃NO

Purity: Min. 95%

Molecular weight: 163.22 g/mol

Ref: 3D-NAA37280