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[ CAS No. 825-25-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 825-25-2
Chemical Structure| 825-25-2
Structure of 825-25-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 825-25-2 ]

CAS No. :825-25-2 MDL No. :MFCD00044678
Formula : C10H14O Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 150.22 Pubchem ID :-
Synonyms :

Safety of [ 825-25-2 ]

Signal Word: Class:
Precautionary Statements: UN#:
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Application In Synthesis of [ 825-25-2 ]

* 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 [ 825-25-2 ]

[ 825-25-2 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 13388-94-8 ]
  • [ 825-25-2 ]
YieldReaction ConditionsOperation in experiment
With sodium azide; PPA
  • 2
  • [ 16424-32-1 ]
  • [ 631-61-8 ]
  • [ 1003-03-8 ]
  • [ 934-42-9 ]
  • [ 825-25-2 ]
  • [ 109645-33-2 ]
  • 3
  • [ 142-04-1 ]
  • [ 120-92-3 ]
  • 4-butyl-8-cyclopentyl-2,3-dihydro-1<i>H</i>-cyclopenta[<i>c</i>]quinoline [ No CAS ]
  • [ 20029-53-2 ]
  • [ 825-25-2 ]
  • 8-aza-7-butyltricyclo[7.4.0.02,6]trideca-1(9),2(6),7,10,12-pentaene [ No CAS ]
YieldReaction ConditionsOperation in experiment
1: 21% 2: 33% 3: 14% 4: 7% In water at 250℃; for 24h;
  • 4
  • [ 103-23-1 ]
  • [ 40566-23-2 ]
  • C15H26O3 [ No CAS ]
  • C17H30O4 [ No CAS ]
  • C18H32O5 [ No CAS ]
  • [ 120587-85-1 ]
  • [ 825-25-2 ]
YieldReaction ConditionsOperation in experiment
at 300℃; for 2.0h;Pyrolysis; Autoclave; Both PAO and DOA were heat-treated at 170, 200,and 300C, respectively, in a 500 mL stainless-steel,magnetically stirred autoclave with the stirring rate of800 r/min. After reaction for 2 h, the reacted sampleswere withdrawn at room temperature. And then, thekinematic viscosity (KV) and total acid number (TAN)of the reaction product were measured according toASTM D445 and ASTM D974 respectively. For conveniencein description, the PAO, DOA, and their oxidized oxidizedsamples under 170, 200, and 300C were abbreviatedas P0, P1, P2, P3 and D0, D1, D2, D3, separately.
  • 5
  • [ 38205-60-6 ]
  • [ 825-25-2 ]
  • (Z)-5-(1-([1,1′-bi(cyclopentylidene)]-2-ylidene)ethyl)-2,4-dimethylthiazole [ No CAS ]
  • (E)-5-(1-([1,1′-bi(cyclopentylidene)]-2-ylidene)ethyl)-2,4-dimethylthiazole [ No CAS ]
  • 6
  • [ 120-92-3 ]
  • [ 20667-16-7 ]
  • [ 6261-30-9 ]
  • [ 4884-25-7 ]
  • [ 27721-49-9 ]
  • C10H15N [ No CAS ]
  • [ 825-25-2 ]
  • [ 1003-03-8 ]
YieldReaction ConditionsOperation in experiment
1: 48.6% 2: 23.2% 3: 5% With ammonia; hydrogen In methanol at 90℃; for 4h; Autoclave;
  • 7
  • [ 110-62-3 ]
  • [ 120-92-3 ]
  • [ 34880-43-8 ]
  • [ 25564-22-1 ]
  • [ 16424-35-4 ]
  • [ 825-25-2 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In water; isopropyl alcohol; at 30℃; for 2h; General procedure: 2-Pentylidenecyclopentanone was obtained viacrotonic condensation of cyclopentanone withn valeric aldehyde. Cyclopentanone in an amount of42 g (0.5 mol), 50 mL of propan-2-ol (as a solvent),and 21.5 g (0.25 mol) of n-valeric aldehyde weresimultaneously placed into a 250-mL flask equippedwith a mechanical stirrer, a thermometer, and a refluxcondenser. A 15% aqueous sodium hydroxide solutionor a 5% piperidine solution in alcohol was added to themixture dropwise in equal portions at 20C. The reaction mixture was stirred for additional 2 h at 30C; theorganic phase was separated from the catalyst, washedto a neutral reaction, and dried over Na2SO4; and thedesired product was isolated by fractional distillationunder vacuum.
  • 8
  • [ 110-62-3 ]
  • [ 120-92-3 ]
  • [ 25564-22-1 ]
  • [ 16424-35-4 ]
  • [ 42558-01-0 ]
  • [ 825-25-2 ]
YieldReaction ConditionsOperation in experiment
With piperidine; In isopropyl alcohol; at 5℃; for 2h; General procedure: 2-Pentylidenecyclopentanone was obtained viacrotonic condensation of cyclopentanone withn valeric aldehyde. Cyclopentanone in an amount of42 g (0.5 mol), 50 mL of propan-2-ol (as a solvent),and 21.5 g (0.25 mol) of n-valeric aldehyde weresimultaneously placed into a 250-mL flask equippedwith a mechanical stirrer, a thermometer, and a refluxcondenser. A 15% aqueous sodium hydroxide solutionor a 5% piperidine solution in alcohol was added to themixture dropwise in equal portions at 20C. The reaction mixture was stirred for additional 2 h at 30C; theorganic phase was separated from the catalyst, washedto a neutral reaction, and dried over Na2SO4; and thedesired product was isolated by fractional distillationunder vacuum.
  • 9
  • [ 110-62-3 ]
  • [ 120-92-3 ]
  • [ 25564-22-1 ]
  • [ 16424-35-4 ]
  • [ 825-25-2 ]
YieldReaction ConditionsOperation in experiment
With sodium hydroxide; In water; isopropyl alcohol; at 30℃; for 2h; General procedure: 2-Pentylidenecyclopentanone was obtained viacrotonic condensation of cyclopentanone withn valeric aldehyde. Cyclopentanone in an amount of42 g (0.5 mol), 50 mL of propan-2-ol (as a solvent),and 21.5 g (0.25 mol) of n-valeric aldehyde weresimultaneously placed into a 250-mL flask equippedwith a mechanical stirrer, a thermometer, and a refluxcondenser. A 15% aqueous sodium hydroxide solutionor a 5% piperidine solution in alcohol was added to themixture dropwise in equal portions at 20C. The reaction mixture was stirred for additional 2 h at 30C; theorganic phase was separated from the catalyst, washedto a neutral reaction, and dried over Na2SO4; and thedesired product was isolated by fractional distillationunder vacuum.
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