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Chemical Structure| 15594-90-8 Chemical Structure| 15594-90-8
Chemical Structure| 15594-90-8

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Heneicosanol is a long-chain primary fatty alcohol that is henicosane in which a hydrogen attached to one of the terminal carbons is replaced by a hydroxy group. It could be isolated from Senecio coluhuapiensis. It presented activity against Staphylococcus aureus (ATCC 29213) and Pseudomonas aeruginosa (ATCC 27853) as well as against Candida albicans (NIM 982879) and C. krusei (ATCC 6258), Botrytis cinerea.

Synonyms: Heneicosyl alcohol

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

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Product Details of Heneicosanol

CAS No. :15594-90-8
Formula : C21H44O
M.W : 312.57
SMILES Code : CCCCCCCCCCCCCCCCCCCCCO
Synonyms :
Heneicosyl alcohol
English Name :Heneicosanol
MDL No. :MFCD00062834
InChI Key :FIPPFBHCBUDBRR-UHFFFAOYSA-N
Pubchem ID :85014

Safety of Heneicosanol

Application In Synthesis of Heneicosanol

* 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 [ 15594-90-8 ]

[ 15594-90-8 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 4276-50-0 ]
  • [ 415974-43-5 ]
  • [ 15594-90-8 ]
YieldReaction ConditionsOperation in experiment
at 150℃; und Erwaermen des Reaktionsprodukts mit aethanol.Kalilauge;
  • 2
  • [ 15594-90-8 ]
  • [ 62127-52-0 ]
YieldReaction ConditionsOperation in experiment
With phosphorus; iodine at 180℃;
  • 3
  • [ 6064-90-0 ]
  • [ 15594-90-8 ]
YieldReaction ConditionsOperation in experiment
With lithium aluminium tetrahydride; diethyl ether
With lithium aluminium tetrahydride In tetrahydrofuran for 1h; Heating;
YieldReaction ConditionsOperation in experiment
With ethanol; sodium
  • 5
  • [ 15594-90-8 ]
  • [ 51227-32-8 ]
YieldReaction ConditionsOperation in experiment
92% With 4 A molecular sieve; pyridinium chlorochromate In dichloromethane at 20℃; for 3h;
  • 6
  • [ 15594-90-8 ]
  • [ 55194-22-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1.1: 92 percent / PCC; molecular sieves 4 Angstroem / CH2Cl2 / 3 h / 20 °C 2.1: Mg / tetrahydrofuran 2.2: 48 percent / tetrahydrofuran / 2 h / 20 °C 3.1: 810 mg / pyridine / CH2Cl2 / 8 h / 20 °C 4.1: Super-hydride / tetrahydrofuran / 12 h / 20 °C 4.2: 370 mg / MCPBA / hexane / 12 h / 20 °C
 

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