82827-57-4

Basic information

• Product Name: 2-benzylphenyl-32-bromopropylether
• Synonyms: 2-benzylphenyl-32-bromopropylether
• CAS NO: 82827-57-4
• Molecular Weight: 305.214
• Mol File: 82827-57-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-benzylphenyl-32-bromopropylether(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzylphenyl-32-bromopropylether(82827-57-4)
• EPA Substance Registry System: 2-benzylphenyl-32-bromopropylether(82827-57-4)

Safety Data

• Hazardous Substances Data: 82827-57-4(Hazardous Substances Data)

Upstream product

• 7563-58-8 Natrium-(2-benzyl-phenolat) 
• 109-64-8 1,3-dibromo-propane 
• 28994-41-4 o-Benzylphenol 
• 627-18-9 1-bromo-3-propanol 

Downstream Products

• 62232-68-2 2-(3-methylaminopropoxy) diphenylmethane hydrochloride 
• 112757-09-2 3-(2-benzylphenoxy)-N-methylpropan-1-amine 
• 785727-41-5 3-(2-benzylphenoxy)-N,N-dimethylpropan-1-amine 

Relevant articles and documents

Dopamine/serotonin receptor ligands. 9.1 oxygen-containing midsized heterocyclic ring systems and nonrigidized analogues. A step toward dopamine D5 receptor selectivity

Eleven-membered heterocycles (dibenz[g,j]-1-oxa-4-azacycloundecenes) and open-chain analogues were synthesized and investigated for affinities to human dopamine receptor subtypes. The moderately rigidized rings displayed nanomolar and subnanomolar Ki values at D1-like receptors with a significant D1 to D2 and a slight D5 to D 1 selectivity. The open-chain analogues showed lower affinities but significant D1 to D2 selectivities. Compound 3 (K i(D5) = 0.57 nmol) showed antagonistic or inverse agonistic binding characteristics in a functional Ca assay.

Phenoxypropylamines: A New Series of Squalene Synthase Inhibitors

-