Basic information Safety Supplier Related

5-(Z-AMINO)-1-PENTANOL

Basic information Safety Supplier Related

5-(Z-AMINO)-1-PENTANOL Basic information

Product Name:
5-(Z-AMINO)-1-PENTANOL
Synonyms:
  • N-CARBOBENZOXY-5-AMINO-1-PENTANOL
  • Z-APE(5)-OL
  • Z-NH-(CH2)5-OH
  • BENZYL N-(5-HYDROXYPENTYL)CARBAMATE
  • 5-(Z-AMINO)-1-PENTANOL
  • 5-[(Benzyloxycarbonyl)amino]-1-pentanol
  • 5-Amino-N-benzyloxycarbonylpentanol
  • N-(5-Hydroxypentyl)-carbamic Acid Phenylmethyl Ester
CAS:
87905-98-4
MF:
C13H19NO3
MW:
237.29
Product Categories:
  • Aromatics Compounds
  • Aromatics
Mol File:
87905-98-4.mol
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5-(Z-AMINO)-1-PENTANOL Chemical Properties

Melting point:
43-47 °C
Boiling point:
408.2±38.0 °C(Predicted)
Density 
1.105±0.06 g/cm3(Predicted)
storage temp. 
Refrigerator
solubility 
Dichloromethane (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form 
Solid
pka
12.68±0.46(Predicted)
color 
White to Pale Gray to Pale Beige
BRN 
4353228
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3

MSDS

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5-(Z-AMINO)-1-PENTANOL Usage And Synthesis

Description

Benzyl (5-hydroxypentyl)carbamate is a linker capable of repairing damaged DNA by binding to the 5'-hydroxyl group on the sugar backbone. It can also bind to DNA ligands and can inhibit cell proliferation in resistant cell lines. However, benzyl (5-hydroxypentyl)carbamate is toxic to cells and can also cause DNA damage and strand breakage.

Chemical Properties

White Solid

Uses

Benzyl (5-hydroxypentyl)carbamate is a linker capable of repairing damaged DNA by binding to the 5'-hydroxyl group on the sugar backbone. Benzyl (5-hydroxypentyl)carbamate can also bind to DNA ligands and can inhibit cell proliferation in resistant cell lines. However, Benzyl (5-hydroxypentyl)carbamate is toxic to cells and can also cause DNA damage and strand breakage.

Synthesis

2508-29-4

501-53-1

87905-98-4

To a stirred mixture of 5-amino-1-pentanol (48.5 mmol, 5.0 g) and sodium bicarbonate (145.4 mmol, 12.2 g) in water (26 mL) was slowly added a solution of benzyl chloroformate (63.1 mmol, 9.0 mL) in THF (26 mL) dropwise at 0-5 °C. After the dropwise addition was completed, the reaction mixture was stirred at room temperature overnight. After completion of the reaction, the organic layer was separated by diluting the reaction mixture with EtOAc and water. The organic layer was washed with brine (2 x 30 mL), dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to remove the solvent. The crude product was dispersed with a minimal amount of cyclohexane and the resulting solid was filtered and dried under vacuum to give 5-(Cbz-amino)-1-pentanol as a white solid (8.2 g, 71%).1H NMR (400 MHz, CDCl3) δ 7.35 (m, 5H), 5.09 (s, 2H), 4.8 (brs, 1H), 3.65 (m, 2H), and 3.20 (m, 2H), 1.50-1.58 (m, 6H), 1.39 (m, 2H).

References

[1] Journal of the American Chemical Society, 2006, vol. 128, # 12, p. 4058 - 4073
[2] Chemical Communications, 2010, vol. 46, # 48, p. 9119 - 9121
[3] Chemistry - A European Journal, 2010, vol. 16, # 6, p. 1754 - 1760
[4] European Journal of Organic Chemistry, 2011, # 12, p. 2346 - 2353
[5] Journal of Medicinal Chemistry, 2002, vol. 45, # 23, p. 5098 - 5111

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