29585-02-2

Basic information

• Product Name: 2-Pentanone, 1-bromo-4-methyl-
• CAS NO: 29585-02-2
• Molecular Formula: C6H11BrO
• Molecular Weight: 179.057
• Mol File: 29585-02-2.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 2-Pentanone, 1-bromo-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pentanone, 1-bromo-4-methyl-(29585-02-2)
• EPA Substance Registry System: 2-Pentanone, 1-bromo-4-methyl-(29585-02-2)

Safety Data

• Hazardous Substances Data: 29585-02-2(Hazardous Substances Data)

Upstream product

• 7732-18-5 water 
• 7726-95-6 bromine 
• 108-10-1 4-methyl-2-pentanone 

Downstream Products

• 1616877-54-3 4-methyl-1-(2-(methylthio)phenoxy)pentan-2-one 
• 27653-95-8 4-methyl-1-(triphenylphosphaneylidene)pentan-2-one 
• 1384267-67-7 4-methyl-1-(2,5-dimethyl-4-bromophenoxy)pentan-2-one 
• 1384267-45-1 C₁₈H₂₈F₂N₂O 
• 1384267-59-7 methyl N-{4-(2,2-difluoro-4-methylpentyloxy)-2,5-dimethylphenyl}formimidate 
• 1384267-69-9 2,2-difluoro-4-methyl-1-(4-amino-2,5-dimethylphenoxy)pentane 
• 1384267-68-8 2,2-difluoro-4-methyl-1-(2,5-dimethyl-4-bromophenoxy)pentane 
• 1373121-57-3 C₁₄H₁₉BrN₂O₂ 
• 1373121-38-0 C₂₂H₂₄N₂O₃ 
• 1260157-86-5 C₂₅H₄₁IO₆ 
• 1048660-74-7 N-(4-methylpentan-2-one)-3-(benzyloxy)-2-methylpyridinate bromide 
• 69798-59-0 1-acetoxy-4-methyl-1-phenylthio-2-pentanone 
• 69798-67-0 1-Chlor-4-methyl-1-phenylthio-2-pentanon 

Relevant articles and documents

Photochemical α-bromination of ketones using N-bromosuccinimide: a simple, mild and efficient method

Aromatic and aliphatic carbonyl compounds undergo facile bromination with N-bromosuccinimide under UV-vis irradiation to give the corresponding α-brominated ketones in good yields, at low temperatures (30 °C), without any catalyst, catalyst support or radical initiator and within a short time.

Discovery of imidazo[2,1- b ]thiazole HCV NS4B inhibitors exhibiting synergistic effect with other direct-acting antiviral agents

The design, synthesis, and SAR studies of novel inhibitors of HCV NS4B based on the imidazo[2,1-b]thiazole scaffold were described. Optimization of potency with respect to genotype 1b resulted in the discovery of two potent leads 26f (EC50 = 16

Highly specific and broadly potent inhibitors of mammalian secreted phospholipases A2

We report a series of inhibitors of secreted phospholipases A2 (sPLA2s) based on substituted indoles, 6,7-benzoindoles, and indolizines derived from LY315920, a well-known indole-based sPLA2 inhibitor. Using the human group X sPLA2 crystal structure, we prepared a highly potent and selective indole-based inhibitor of this enzyme. Also, we report human and mouse group IIA and IIE specific inhibitors and a substituted 6,7-benzoindole that inhibits nearly all human and mouse sPLA 2s in the low nanomolar range.