876322-73-5

Basic information

• Product Name: Benzaldehyde, 4-aMino-2-(trifluoroMethyl)-
• Synonyms: Benzaldehyde, 4-aMino-2-(trifluoroMethyl)-
• CAS NO: 876322-73-5
• Molecular Formula: C₈H₆F₃NO
• Molecular Weight: 189.1345496
• Mol File: 876322-73-5.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: Benzaldehyde, 4-aMino-2-(trifluoroMethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4-aMino-2-(trifluoroMethyl)-(876322-73-5)
• EPA Substance Registry System: Benzaldehyde, 4-aMino-2-(trifluoroMethyl)-(876322-73-5)

Safety Data

• Hazardous Substances Data: 876322-73-5(Hazardous Substances Data)

Usage

General Description

Benzaldehyde, 4-amino-2-(trifluoromethyl)- is a chemical compound with the molecular formula C8H7F3N. It is a white to light yellow crystalline solid with a faint odor, and it is primarily used in the synthesis of pharmaceuticals and agrochemicals. Benzaldehyde, 4-amino-2-(trifluoromethyl)- is also used as a building block for various organic reactions and serves as an intermediate in the production of dyes, perfumes, and flavoring agents. Additionally, Benzaldehyde, 4-amino-2-(trifluoromethyl)- is a versatile reagent in organic chemistry and can undergo various chemical transformations to yield a wide range of functionalized compounds. Furthermore, this chemical has been studied for its potential biological and pharmacological activities, making it an interesting target for further research and development.

Upstream product

• 98-16-8 3-trifluoromethylaniline 
• 109-94-4 formic acid ethyl ester 
• 50551-17-2 4-nitro-2-(trifluoromethyl)benzaldehyde 
• 320-37-6 4-nitro-2-(trifluoromethyl)benzoic acid 
• 859027-06-8 (4-nitro-2-(trifluoromethyl)phenyl)methanol 
• 654-70-6 4-amino-2-trifluoromethylbenzonitrile 

Downstream Products

• 654-70-6 4-amino-2-trifluoromethylbenzonitrile 
• 694499-26-8 4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylaniline 
• 1186206-79-0 ALW-II-41-27 
• 872332-67-7 3-amino-N-(4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)-4-methylbenzamide 
• 872332-66-6 N-(4-((4-ethylpiperazin-1-yl)methyl)-3-(trifluoromethyl)phenyl)-4-methyl-3-nitrobenzamide 
• 630125-91-6 4-(4-ethylpiperazin-1-ylmethyl)-3-trifluoromethylphenylamine 
• 943319-70-8 ponatinib 
• 900254-46-8 (4-amino-2-(trifluoromethyl)phenyl)methanol 

Relevant articles and documents

A Putative Single-Photon Emission CT Imaging Tracer for Erythropoietin-Producing Hepatocellular A2 Receptor

Erythropoietin-producing hepatocellular (Eph) receptors are receptor tyrosine kinases involved in cell-cell contact. The EphA2 receptor is associated with cancer proliferation and migration. Therefore, EphA2 receptor imaging has the potential for cancer d

Highly chemoselective intermolecular cross-benzoin reactions using an: Ad hoc designed novel N-heterocyclic carbene catalyst

The design of a novel N-heterocyclic carbene catalyst incorporating a bulky yet highly electron-deficient N-aryl substituent has allowed the development of an efficient protocol for the first highly chemoselective intermolecular benzoin condensations between two non-identical aromatic aldehydes.

Syntheses of a triad of Flt3 kinase inhibitors: From bench to pilot plant

We have designed and developed an alternative synthesis for the manufacturing of a triad of Flt3 kinase inhibitors (AST487, ATH686, and AUZ454) to support clinical assessments of patients with Flt3-dependent tumor diseases. The new synthesis is convergent