887604-02-6

Basic information

• Product Name: (((13-bromotridecyl)oxy)methyl)benzene
• Synonyms: (((13-bromotridecyl)oxy)methyl)benzene
• CAS NO: 887604-02-6
• Molecular Weight: 369.385
• Mol File: 887604-02-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (((13-bromotridecyl)oxy)methyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (((13-bromotridecyl)oxy)methyl)benzene(887604-02-6)
• EPA Substance Registry System: (((13-bromotridecyl)oxy)methyl)benzene(887604-02-6)

Safety Data

• Hazardous Substances Data: 887604-02-6(Hazardous Substances Data)

Upstream product

• 505-52-2 brassylic acid 
• 13362-52-2 1,13-tridecanediol 
• 116754-58-6 13-bromo-1-tridecylalcohol 
• 100-39-0 benzyl bromide 

Downstream Products

• 1350292-76-0 1,1'-di-O-benzyl-3,3'-O-((16,19-methylidene)tetratriacontane-1,34-diyl)-di-sn-glycerol 
• 812653-06-8 14-[6-methoxy-1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-tetradecan-1-ol 
• 651331-69-0 14-[4-methoxy-1-(4-methoxybenzsulfonyl)-1H-indole-3-yl]-tetradecane-1-ol 
• 651331-73-6 14-[5-methoxy-1-(4-methoxybenzsulfonyl)-1H-indole-3-yl]-tetradecane-1-ol 
• 411218-11-6 14-[1-(4-methoxy-benzenesulfonyl)-1H-indol-3-yl]-tetradecan-1-ol 
• 887604-20-8 1-(15-Benzyloxy-pentadec-1-ynyl)-2,3,4,5-tetramethoxy-benzene 
• 887604-15-1 1-(15-Benzyloxy-pentadec-1-ynyl)-2,4,5-trimethoxy-benzene 
• 887604-10-6 2-(15-Benzyloxy-pentadec-1-ynyl)-1,4-dimethoxy-benzene 

Relevant articles and documents

Systematic synthesis of novel phosphoglycolipid analogues as potential agonists of GPR55

Rhodopsin-like G protein-coupled receptor (GPCR) GPR55 is attracting attention as a pharmaceutical target, because of its relationship with various physiological and pathological events. Although GPR55 was initially deorphanized as a cannabinoid receptor,

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.