111-24-0 | 1,5-Dibromopentane

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$13.00	$9.00
25g	98%	in stock	$15.00	$11.00
100g	98%	in stock	$21.00	$15.00
500g	98%	in stock	$26.00	$18.00

Description

• Catalog Number: AB43197
• Chemical Name: 1,5-Dibromopentane
• CAS Number: 111-24-0
• Molecular Formula: C5H10Br2
• Molecular Weight: 229.9409
• MDL Number: MFCD00000268
• SMILES: BrCCCCCBr
• NSC Number: 5373

Computed Properties

• Complexity: 25.3
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Rotatable Bond Count: 4
• XLogP3: 2.8

Literature

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  PloS one 20120101

• Growth of a tropical marine yeast Yarrowia lipolytica NCIM 3589 on bromoalkanes: relevance of cell size and cell surface properties.

  Yeast (Chichester, England) 20111001

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  Acta crystallographica. Section E, Structure reports online 20110701

• 3-(Piperidin-1-ium-1-yl)-6-azoniaspiro-[5.5]undecane dibromide monohydrate.

  Acta crystallographica. Section E, Structure reports online 20110601

• 2-(5-Bromo-pent-yl)-4-chloro-5-[2-(4-meth-oxy-phen-yl)ethyl-amino]-pyridazin-3(2H)-one.

  Acta crystallographica. Section E, Structure reports online 20100901

• Design of group IIA secreted/synovial phospholipase A(2) inhibitors: an oxadiazolone derivative suppresses chondrocyte prostaglandin E(2) secretion.

  PloS one 20100101

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  Acta crystallographica. Section E, Structure reports online 20091201

• Synthesis and evaluation of 1-(1-(Benzo[b]thiophen-2-yl)cyclohexyl)piperidine (BTCP) analogues as inhibitors of trypanothione reductase.

  ChemMedChem 20090803

• Expeditious and convenient synthesis of pregnanes and its glycosides as potential anti-dyslipidemic and anti-oxidant agents.

  Bioorganic & medicinal chemistry 20070701

• Effect of alterations of key active site residues in O6-alkylguanine-DNA Alkyltransferase on its ability to modulate the genotoxicity of 1,2-dibromoethane.

  Chemical research in toxicology 20070101

• Synthesis and biological properties of 2-hydroxy-1-(1-phenyltetralyl)piperidine and some of its intermediates as derivatives of phencyclidine.

  Arzneimittel-Forschung 20050101

• Novel spirocyclic pyrrolidones as P2/P1 mimetics in potent inhibitors of HIV-1 protease.

  Bioorganic & medicinal chemistry letters 20021202