144878-52-4

Basic information

• Product Name: 17-benzyloxy-1-bromoheptadecane
• Synonyms: 17-benzyloxy-1-bromoheptadecane
• CAS NO: 144878-52-4
• Molecular Weight: 425.493
• Mol File: 144878-52-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 17-benzyloxy-1-bromoheptadecane(CAS DataBase Reference)
• NIST Chemistry Reference: 17-benzyloxy-1-bromoheptadecane(144878-52-4)
• EPA Substance Registry System: 17-benzyloxy-1-bromoheptadecane(144878-52-4)

Safety Data

• Hazardous Substances Data: 144878-52-4(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 1611-56-9 1-Bromo-11-hydroxyundecane 
• 345909-09-3 15-bromo-pentadecanal 
• 338389-27-8 17-bromoheptadecan-1-ol 
• 629-03-8 1 ,6-dibromohexane 
• 144878-51-3 11-bromoundecan-1-yl benzyl ether 
• 102180-75-6 17-bromo-heptadecanoic acid ethyl ester 
• 59101-27-8 15-bromopentadecane-1-ol 
• 1027018-08-1 (E)-17-Bromo-heptadec-2-enoic acid ethyl ester 

Downstream Products

• 812653-11-5 18-[4,5-dimethoxy-1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-octadecan-1-ol 
• 812653-13-7 18-[5,6-dimethoxy-1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-octadecan-1-ol 
• 651331-75-8 18-[5-methoxy-1-(4-methoxybenzsulfonyl)-1H-indole-3-yl]-octadecane-1-ol 
• 812653-08-0 18-[6-methoxy-1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-octadecan-1-ol 
• 651331-71-4 18-[4-methoxy-1-(4-methoxybenzsulfonyl)-1H-indole-3-yl]-octadecane-1-ol 
• 812653-05-7 18-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-octadecan-1-ol 
• 144878-53-5 19-(17'-benzyloxyheptadecyl)-24-octadecyl-23-dotetraconten-19-ol 
• 144878-57-9 1-benzyloxy-18-phenyloctadecane 
• 144878-54-6 19-(17'-hydroxyheptadecyl)-24-octadecyl-23-dotetraconten-19-ol 
• 68141-06-0 18-phenyloctadecanol 

Relevant articles and documents

Effects of indole fatty alcohols on the differentiation of neural stem cell derived neurospheres

In a search for inducers of neuronal differentiation to treat neurodegenerative diseases such as Alzheimer's disease, a series of indole fatty alcohols (IFAs) were prepared, 13c (n = 18) was able to promote the differentiation of neural stem cell derived neurospheres into neurons at a concentration of 10 nM. Analysis of the expression of the Notch pathway genes in neurospheres treated during the differentiation phase with 13c (n = 18) revealed a significant decrease in the transcription of the Notch 4 receptor.

Synthesis of a Branched High Molecular Weight Hydrocarbon with a Single Hydroxy Group as Polar Stationary Phase for Gas Chromatography

The synthesis of 18,23-dioctadecyl-1-hentetracontanol (12), a high molecular weight solvent employed as a polar stationary phase for gas chromatography, having only one functional group, is described.This stationary phase allows the study of polar forces in the separation process.