3714-77-0

Basic information

• Product Name: BENZALDEHYDE, 2,6-DICHLORO-, OXIME, (Z)-
• Synonyms: BENZALDEHYDE, 2,6-DICHLORO-, OXIME, (Z)-;(Z)-2,6-Dichlorobenzaldehyde oxime
• CAS NO: 3714-77-0
• Molecular Formula: C₇H₅Cl₂NO
• Molecular Weight: 190.0267
• Mol File: 3714-77-0.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: BENZALDEHYDE, 2,6-DICHLORO-, OXIME, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: BENZALDEHYDE, 2,6-DICHLORO-, OXIME, (Z)-(3714-77-0)
• EPA Substance Registry System: BENZALDEHYDE, 2,6-DICHLORO-, OXIME, (Z)-(3714-77-0)

Safety Data

• Hazardous Substances Data: 3714-77-0(Hazardous Substances Data)

Upstream product

• 83-38-5 2,6-dichlorobenzaldehyde 

Downstream Products

• 6579-27-7 2,6-Dichloro-N-hydroxybenzenecarboximidoyl chloride 
• 774605-35-5 ethyl 3-(2,6-dichlorophenyl)-5-(propan-2-yl)-1,2-oxazole-4-carboxylate 
• 946426-89-7 4-(hydroxymethyl)-5-cyclopropyl-3-(2,6-dichlorophenyl)isoxazole 

Relevant articles and documents

HETEROCYCLIC FXR MODULATORS

The present technology is directed to compounds of formula (I), compositions, and methods related to modulation of FXR. In particular, the present compounds and compositions may be used to treat FXR-mediated disorders and conditions, including, e.g., liver disease, hyperlipidemia, hypercholesteremia, obesity, metabolic syndrome, cardiovascular disease, gastrointestinal disease, and atherosclerosis, and renal disease.

Titanium oxide (TiO2) catalysed one-step Beckmann rearrangement of aldehydes and ketones in solvent free conditions

In the presence of titanium oxide (TiO2) and without any additional organic solvents, Beckmann rearrangement of several ketones and aldehydes was performed in good yield.

One-step Beckmann rearrangement from carbonyl compounds and hydroxylamine hydrochloride in Al2O3/CH3SO3H (AMA) as a new reagent

A facile and efficient synthetic procedure, for one-step Beckmann rearrangement of aldehydes and ketones with hydroxylamine hydrochloride and Al2O3/CH3SO3H (AMA) has been developed; cyclohexanone has been converted into ε-caprolactam in a quantitative yield.