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Chemical Structure| 557-61-9 Chemical Structure| 557-61-9
Chemical Structure| 557-61-9

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1-Octacosanol is a straight-chain aliphatic 28-carbon fatty alcohol with physiological functions such as cholesterol reduction, anti-fatigue, and enhanced endurance, commonly used in health foods and nutritional supplements.

Synonyms: Montanyl Alcohol; Octacosyl alcohol; NSC 57768

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of 1-Octacosanol

CAS No. :557-61-9
Formula : C28H58O
M.W : 410.76
SMILES Code : CCCCCCCCCCCCCCCCCCCCCCCCCCCCO
Synonyms :
Montanyl Alcohol; Octacosyl alcohol; NSC 57768
English Name :Octacosan-1-ol
MDL No. :MFCD00044770
InChI Key :CNNRPFQICPFDPO-UHFFFAOYSA-N
Pubchem ID :68406

Safety of 1-Octacosanol

Application In Synthesis of 1-Octacosanol

* 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 [ 557-61-9 ]

[ 557-61-9 ] Synthesis Path-Downstream   1~14

  • 4
  • [ 557-61-9 ]
  • [ 145205-03-4 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With dicyclohexyl-carbodiimide In pyridine at 50 - 55℃;
  • 5
  • [ 557-61-9 ]
  • [ 16331-21-8 ]
YieldReaction ConditionsOperation in experiment
100% With N-Bromosuccinimide; triphenylphosphine In dichloromethane at 0 - 25℃; for 1h; 1.1 Octacosane-1-bromide Added PPh3 (3.83 g, 14.61 mmol) to a DCM solution (50 mL) of octacosan-1-ol (5 g, 12.17 mmol). Then, add Nbromosuccinimide(2.60 g, 14.61 mmo) to the mixture at 0°C. Stir the mixture at 25°C for 1 h. Add a saturated Na2SO3solution (50 mL), and extract the aqueous phase with DCM (50 mL x 3). Wash the combined organic phases with saturatedbrine (100 mL), dry with anhydrous Na2SO4, filter, and concentrate under reduced pressure. Purify the crude product bysilica gel flash column chromatography (eluent: petroleum ether) to obtain ctacosane-1-bromide (5.77 g, 12.18 mmol, yield100.00%), which is a white solid. 1H NMR (400 MHz, CDCl3) δ = 3.42 (t, J = 7.6 Hz, 2H), 1.95 - 1.80 (m, 2H), 1.44 (s, 2H), 1.30 - 1.24 (m, 48H), 0.89(t, J = 6.8 Hz, 3H).
With sulfuric acid; hydrogen bromide at 90 - 110℃;
  • 6
  • [ 55682-92-3 ]
  • [ 557-61-9 ]
YieldReaction ConditionsOperation in experiment
With lithium aluminium tetrahydride In tetrahydrofuran for 1h; Heating;
  • 7
  • [ CAS Unavailable ]
  • [ 557-61-9 ]
YieldReaction ConditionsOperation in experiment
With lithium aluminium tetrahydride In tetrahydrofuran Heating; Yield given;
  • 8
  • [ 148172-69-4 ]
  • [ 557-61-9 ]
YieldReaction ConditionsOperation in experiment
With hydrogen In ethanol
  • 9
  • [ 102607-46-5 ]
  • [ 557-61-9 ]
  • [ 25522-33-2 ]
YieldReaction ConditionsOperation in experiment
1: 8 mg 2: 50 mg With potassium hydroxide In chloroform for 1h; Heating;
  • 10
  • [ 87538-97-4 ]
  • [ 557-61-9 ]
  • [ 506-50-3 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide In ethanol for 5h; Heating;
  • 11
  • [ 557-61-9 ]
  • [ 63029-02-7 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With pyridine In tetrachloromethane Ambient temperature;
  • 12
  • [ 557-61-9 ]
  • [ 112-67-4 ]
  • [ 78509-52-1 ]
YieldReaction ConditionsOperation in experiment
With pyridine In tetrachloromethane Ambient temperature;
  • 13
  • [ CAS Unavailable ]
  • [ 557-61-9 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride In methanol for 5h; Heating;
  • 14
  • [ 180465-33-2 ]
  • [ 557-61-9 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride In methanol for 5h; Heating;
Multi-step reaction with 2 steps 1: KOH / methanol / 5 h / Heating 2: HCl / methanol / 5 h / Heating
 

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