31084-55-6

Basic information

• Product Name: Benzenamine, N-butyl-3-methoxy-
• CAS NO: 31084-55-6
• Molecular Formula: C11H17NO
• Molecular Weight: 179.262
• Mol File: 31084-55-6.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-butyl-3-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-butyl-3-methoxy-(31084-55-6)
• EPA Substance Registry System: Benzenamine, N-butyl-3-methoxy-(31084-55-6)

Safety Data

• Hazardous Substances Data: 31084-55-6(Hazardous Substances Data)

Upstream product

• 542-69-8 1-iodo-butane 
• 536-90-3 m-Anisidine 
• 109-74-0 propyl cyanide 
• 123-72-8 butyraldehyde 
• 555-03-3 3-nitroanisole 
• 109-65-9 1-bromo-butane 
• 2398-37-0 3-methoxyphenyl bromide 
• 109-73-9 N-butylamine 
• 10174-66-0 N¹,N³-dibutylmalonamide 
• 766-85-8 3-methoxy-1-iodobenzene 
• 132118-40-2 N-(3-methoxyphenyl)butyramide 

Downstream Products

• 536-90-3 m-Anisidine 
• 123-72-8 butyraldehyde 
• 75813-77-3 N-(4-Acetoxy-3-methoxyphenyl)acetamide 
• 588-16-9 m-methoxyacetanilide 
• 1307740-94-8 2-(4-butylamino-2-methoxyphenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol 
• 1307741-63-4 2-bromo-N-butyl-N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-3-methoxyphenyl]-5-methoxybenzamide 
• 1307741-11-2 2-(2-benzyloxy-1,1,1,3,3,3-hexafluoropropan-2-yl)-5-butyl-1-methoxyphenanthridin-6(5H)-one 
• 1307741-10-1 N-butyl-N-[4-(2-benzyloxy-1,1,1,3,3,3-hexafluoropropan-2-yl)-3-methoxyphenyl]-2-iodobenzamide 
• 1307741-03-2 N-butyl-N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-3-methoxyphenyl]-2-iodo-benzamide 

Relevant articles and documents

Precise Labeling and Tracking of Lipid Droplets in Adipocytes Using a Luminescent ZnSalen Complex

Designing two-photon probes for precise labeling of lipid droplets (LDs) and monitoring LD dynamics in adipocytes is of great significance to understand LD homeostasis. We herein report that a luminescent metal complex LD-TPZn can specifically image LDs in adipose cells and tissue using one- or two-photon fluorescence microscopy. Importantly, LD-TPZn exhibited higher specificity to LDs than the commercial dyes Nile Red and Bodipy 493/503, probably due to different cellular uptake pathways, that is, clathrin-mediated endocytosis and non-selectively passive diffusion, respectively. More importantly, LD-TPZn can be applied as a two-photon LD probe to image adipose tissue, one of the most challengeable tissues for traditional one-photon fluorescence microscope imaging due to the strong light scattering. Most importantly, LD-TPZn can be used to monitor LD growth during adipogenesis of preadipocytes, which is highly desirable to unravel the relationship between LD homeostasis and metabolic diseases.

A recyclable Cu-catalyzed C-N coupling reaction in water and its application to synthesis of imidazo[1,2-a]quinoxaline

Polystyrene-supported pyrrole-2-carbohydrazide (PSP) was synthesized and combined with CuI to make up a recyclable heterogeneous catalytic system for Ullmann-type C-N coupling reaction in water. In which, a variety of functionalized aryl halides animated efficiently with anilines, benzylamine, aliphatic amines, and imidazole. its preliminary application resulted in a more practical synthesis of imidazo[1,2-a]quinoxaline.

SUBSTITUTED SULFONAMIDES USEFUL AS ANTIAPOPTOTIC BCL INHIBITORS

Disclosed are compounds of Formula (I), or a pharmaceutically acceptable salt thereof, wherein: W and Q and G are defined herein. Also disclosed are methods of using such compounds as inhibitors of Bcl-2 family antiapoptotic proteins for the treatment of cancer; and pharmaceutical compositions comprising such compounds.