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Chemical Structure| 4048-33-3 Chemical Structure| 4048-33-3
Chemical Structure| 4048-33-3

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6-Amino-1-hexanol is a hexanol derivative with an amino group, used in the preparation of specialty chemicals and as a building block.

4.5 *For Research Use Only !

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Product Details of 6-Amino-1-hexanol

CAS No. :4048-33-3
Formula : C6H15NO
M.W : 117.19
SMILES Code : OCCCCCCN
MDL No. :MFCD00008241
InChI Key :SUTWPJHCRAITLU-UHFFFAOYSA-N
Pubchem ID :19960

Safety of 6-Amino-1-hexanol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 6-Amino-1-hexanol

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 4048-33-3 ]

[ 4048-33-3 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 1194-21-4 ]
  • [ 4048-33-3 ]
  • 2-Amino-6-(6-hydroxy-hexylamino)-3H-pyrimidin-4-one [ No CAS ]
  • 2
  • [ 4048-33-3 ]
  • [ 1655-06-7 ]
  • (1S,2S)-2-Hydroxy-cyclohexanecarboxylic acid 6-[((1S,2S)-2-hydroxy-cyclohexanecarbonyl)-amino]-hexyl ester [ No CAS ]
  • 3
  • [ 4048-33-3 ]
  • [ 28920-43-6 ]
  • [ 127903-20-2 ]
YieldReaction ConditionsOperation in experiment
98% With sodium carbonate; In 1,4-dioxane; at 0 - 25℃; for 12h; 1) Dissolve 5.3 g of fluorenyl methoxycarbonyl chloride in 40 mL of 1,4-dioxane, Add 2g of 6-amino-1-hexanol at 0C, Fully dissolve, then slowly add 20mL of 10% Na2CO3 solution, Reaction at 25 for 12h, The product was extracted with methanol-dichloromethane (methanol, dichloromethane volume ratio 1:19), Combine the organic phases, spin dry the solvent on a rotary evaporator, Use a mixed solvent (consisting of dichloromethane, ethyl acetate and petroleum ether in a volume ratio of 1:3:6) Obtained (yield: 98%);
97% With sodium carbonate; In 1,4-dioxane; water; at 0 - 20℃; for 1h; Fmoc-6-aminohexanol (3). 6-Amino-hexan-1-ol (1.5 g, 12 mmol) was added to a vigorously stirred solution of Na2CO3 in H2O at 0 C. Dioxane (30 mL) was added, providing an opaque mixture. A solution of FmocCl, in dioxane (36 mL) was added dropwise at 0 C. The mixture was then allowed to warm to room temperature and was stirred for 1 hour. AcOEt (300 mL) was added, followed by HCl 0.1M (200 mL). The organic layer was washed with H2O (200 mL) and brine (50 mL), then dried over Na2SO4, filtered and concentrated. The crude product was purified by flash chromatography (CH2Cl2/MeOH, 97:3 to 90:10) to afford 3 as a white solid (3.95 g, 97%).
  • 6
  • [ 4048-33-3 ]
  • [ 117-78-2 ]
  • 9,10-dioxo-9,10-dihydro-anthracene-2-carboxylic acid (6-hydroxy-hexyl)-amide [ No CAS ]
  • 7
  • [ 4048-33-3 ]
  • [ 78078-92-9 ]
  • [ 1234567-23-7 ]
  • 8
  • [ 4048-33-3 ]
  • [ 5780-66-5 ]
  • C11H17N3O [ No CAS ]
  • 9
  • [ 4048-33-3 ]
  • [ 4506-66-5 ]
  • N<SUP>1</SUP>,N<SUP>2</SUP>,N<SUP>4</SUP>,N<SUP>5</SUP>-tetrakis (6-hydrohexyl)-2,5-diamino-1,4-benzoquinonediimine [ No CAS ]
 

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