96154-40-4

Basic information

• Product Name: Benzene, [[(3,7-dimethyl-6-octenyl)oxy]methyl]-
• CAS NO: 96154-40-4
• Molecular Formula: C17H26O
• Molecular Weight: 246.393
• Mol File: 96154-40-4.mol

Chemical Properties

• CAS DataBase Reference: Benzene, [[(3,7-dimethyl-6-octenyl)oxy]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [[(3,7-dimethyl-6-octenyl)oxy]methyl]-(96154-40-4)
• EPA Substance Registry System: Benzene, [[(3,7-dimethyl-6-octenyl)oxy]methyl]-(96154-40-4)

Safety Data

• Hazardous Substances Data: 96154-40-4(Hazardous Substances Data)

Upstream product

• 106-22-9 Citronellol 
• 100-39-0 benzyl bromide 
• 100-44-7 benzyl chloride 
• 7540-51-4 (S)-3,7-dimethyl-6-octen-1-ol 

Downstream Products

• 106-22-9 Citronellol 
• 67245-14-1 2,6-dimethyl-2,3-epoxy-8-(benzyloxy)octane 
• 123300-77-6 (E)-8-hydroxy-3,7-dimethyl-6-octenyl benzyl ether 
• 139372-97-7 (E)-8-Benzyloxy-2,6-dimethyl-oct-2-enal 
• 138604-47-4 (S)-6-benzyloxy-4-methylhexanal 
• 83541-13-3 (R)-(+)-6-(benzyloxy)-4-methylhexanal 
• 87359-89-5 4-methyl-6-(benzyloxy)-1-hexanal 
• 689221-14-5 benzyl 3,7-dimethyl-7-fluoroctyl ether 
• 106-21-8 tetrahydrogeraniol 
• 128386-36-7 (E)-chloro-3,7-dimethyl-6-octenyl benzyl ether 
• 102745-42-6 (4R)-methyl-6-(benzyloxy)hexanoic acid 
• 1088706-44-8 C₂₅H₃₂N₂O₃ 
• 1088706-46-0 C₃₁H₃₇NO 
• 123300-83-4 ((E)-8-Ethoxy-3,7-dimethyl-oct-6-enyloxymethyl)-benzene 

Relevant articles and documents

Boron trifluoride-mediated alkylation of diphenylphosphine with tert-alkyl fluoride

(Chemical Equation Presented) Treatment of tertiary alkyl fluoride with diphenylphosphine in the presence of a stoichiometric amount of boron trifluoride etherate yields the corresponding tert-alkyldiphenylphosphine despite the coexistence of the strong L

Enzymatic synthesis of β-mannosyl phosphates on solid support

Synthetic bifunctional analogues 4a,b and 14 of dolichol phosphate 1 were attached to solid support and were shown to be substrates for Dol-P-Man synthase.

Products Active on Mosquitoes: Part III - Synthesis of Biologically Active 3,7-Dimethyl-6-octene-1,8-diol Diethers

Mixed diethers (IIIa-s) have been prepared from 8-hydroxy-monoethers (IIa-g) which in turn have been obtained from citronellyl ethers (Ia-g) by selenium oxidation.Most of the diethers are oviposition deterrent, while some of them also show inhibition towards the development of mosquitoes.

Synthesis of Both 2,3-erythro- and 2,3-threo-Isomers of Aplidiasphingosine, a Marine Terpenoid

Both 2,3-erythro- and 2,3-threo-isomers of aplidiasphingosine were synthesized.By examining their 13C NMR spectra, 2,3-threo- and 13,14-erythro-relative configurations are proposed for aplidiasphingosine.

Synthesis of the Proposed Penultimate Biosynthetic Triene Intermediate of Monensin A

A convergent chiral synthesis of the putative biosynthetic triene precursor, 2b, has been accomplished.Our strategy entails the successive assembly of three key chiral synthons, prepared by enzymatic and microbial techniques.