25996-10-5

Basic information

• Product Name: 2,6-Octadiene, 1-bromo-3,7-dimethyl-, (2Z)-
• CAS NO: 25996-10-5
• Molecular Formula: C10H17Br
• Molecular Weight: 217.149
• Mol File: 25996-10-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,6-Octadiene, 1-bromo-3,7-dimethyl-, (2Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Octadiene, 1-bromo-3,7-dimethyl-, (2Z)-(25996-10-5)
• EPA Substance Registry System: 2,6-Octadiene, 1-bromo-3,7-dimethyl-, (2Z)-(25996-10-5)

Safety Data

• Hazardous Substances Data: 25996-10-5(Hazardous Substances Data)

Upstream product

• 115-95-7 linalool acetate 
• 78-70-6 3,7-dimethylocta-1,6-dien-3-ol 

Downstream Products

• 107259-60-9 catechol mononeryl ether 
• 51116-98-4 6-((Z)-3,7-Dimethyl-octa-2,6-dienyloxy)-3-formyl-2-hydroxy-4-methoxy-benzoic acid methyl ester 
• 27644-06-0 2,6-dimethyl-1-phenyl-2-vinylhept-5-en-1-ol 
• 796965-82-7 Z-(4S,5R,2'S)-3,4-dimethyl-5-phenyl-1-(2'-benzyloxy-5',9'-dimethyldeca-4',8'-dienoyl)-imidazolidin-2-one 
• 833480-04-9 (Z)-4,8-dimethylnona-3,7-dienal diphenyl dithioacetal 
• 16106-95-9 (2Z,6Z)-farnesol 
• 19954-66-6 ethyl 3,7,11-trimethyl-2ξ,6Z,10-dodecatrienoate 
• 586-62-9 Terpinolene 
• 5989-27-5 D-limonene 
• 5989-54-8 (-)-(S)-limonene 
• 138-86-3 limonene. 
• 111-02-4 2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene 
• 77547-18-3 (3E,7E)-(1S,11S)-10-Benzenesulfonyl-4,8,12,15,15-pentamethyl-bicyclo[9.3.1]pentadeca-3,7,12-triene 
• 67779-95-7 (2E,6E,12Z)-14-Benzenesulfonyl-9-isopropenyl-2,6,12-trimethyl-tetradeca-2,6,12-trienoic acid methyl ester 

Relevant articles and documents

Synthesis and antimycobacterial activity of agelasine E and analogs

Agelasine E, previously isolated from the marine sponge Agelas nakamurai, has been synthesized for the first time, together with analogs with various terpenoid side chains. Treatment of N6-methoxy-9-methyl-9H-purin-6- amine with allylic bromides gave the desired 7,9-dialkylpurinium salts together with minor amounts of the N6-alkylated isomer. The N 6-methoxy group was finally removed reductively. 1H- 15N HMBC and 1H-15N HSQC NMR spectroscopy gave additional information on tautomerism and charge delocalization in the purine derivatives studied. The heterocyclic products were screened for activity against Mycobacterium tuberculosis and agelasine analogs carrying a relatively long terpenoid substituent in the purine 7-position and a methoxy group at N-6 were potent inhibitors of bacterial growth. Since agelasine analogs with the geranylgeranyl chain at N-7 exhibited antimicrobial activity, several strategies for synthesis of geometrically pure (2E,6E,10E)-geranylgeranyl bromide from geranyllinalool were evaluated. The Royal Society of Chemistry 2005.