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[ CAS No. 4313-56-8 ] {[proInfo.proName]}

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Chemical Structure| 4313-56-8
Chemical Structure| 4313-56-8
Structure of 4313-56-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 4313-56-8 ]

CAS No. :4313-56-8 MDL No. :MFCD12198034
Formula : C7H15NO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 129.20 Pubchem ID :-
Synonyms :

Safety of [ 4313-56-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 4313-56-8 ]

* 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 [ 4313-56-8 ]

[ 4313-56-8 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 4313-56-8 ]
  • [ 207557-35-5 ]
  • (S)-1-[2-(1-Hydroxymethyl-cyclohexylamino)-acetyl]-pyrrolidine-2-carbonitrile [ No CAS ]
  • 2
  • [ 4313-56-8 ]
  • [ 188593-96-6 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 97 percent / MgSO4 / diethyl ether / 18 h / Ambient temperature 2: 94 percent / NaBH4 / methanol / 18 h / Ambient temperature
  • 3
  • [ 4313-56-8 ]
  • [ 13544-44-0 ]
  • (1-((2-chloro-5-iodopyrimidin-4-yl)amino)cyclohexyl)methanol [ No CAS ]
YieldReaction ConditionsOperation in experiment
1.5 g With sodium hydrogencarbonate; In N,N-dimethyl acetamide; at 80℃; for 4h; To a solution of <strong>[13544-44-0]2,4-dichloro-5-iodopyrimidine</strong> (247, 2.7 g, 9.8 mmol) in DMA (20 mL) was added (1-aminocyclohexyl)methanol (244, 1.4 g, 10.8 mmol) and NaHCO3 (5 g, 59.5 mol).The reaction was stirred at 80 C for 4 h. After cooling to room temperature, the reaction mixture was quenched with water (40 mL) and extracted with EtOAc (50 mL x 2). Thecombined organic phases were concentrated in vacuo to afford the residue, which was purified by column chromatography to afford (1-((2-chloro-5-iodopyrimidin-4- yl)amino)cyclohexyl)methanol (248, 1.5 g, 4.1 mmol). MS (ESI): m/z 368 [M + Hj
  • 4
  • [ 381-88-4 ]
  • [ 4313-56-8 ]
  • 2-ethyl-2-(trifluoromethyl)-3-oxa-1-azaspiro[4.5]decane [ No CAS ]
YieldReaction ConditionsOperation in experiment
53% With toluene-4-sulfonic acid at 120℃; for 16h; Sealed tube; Molecular sieve;
  • 5
  • [ 2955-62-6 ]
  • [ 4313-56-8 ]
  • methyl 3-(2-ethyl-3-oxa-1-azaspiro[4.5]decan-2-yl)propanoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
38% With toluene-4-sulfonic acid In toluene for 16h; Dean-Stark; Reflux;
  • 6
  • [ 4313-56-8 ]
  • [ 265664-91-3 ]
  • 2-((benzyloxy)methyl)-2-ethyl-3-oxa-1-azaspiro[4.5]decane [ No CAS ]
  • 7
  • [ 1123-86-0 ]
  • [ 4313-56-8 ]
  • 2-cyclohexyl-2-ethyl-3-oxa-1-azaspiro[4.5]decane [ No CAS ]
  • 8
  • [ 14371-10-9 ]
  • [ 2039-93-2 ]
  • [ 4313-56-8 ]
  • 3-ethyl-2,3-diphenylcyclobutane-1-carbaldehyde [ No CAS ]
  • 3-ethyl-2,3-diphenylcyclobutane-1-carbaldehyde [ No CAS ]
YieldReaction ConditionsOperation in experiment
93 % ee Stage #1: (E)-3-phenylpropenal; (1-aminocyclohexyl)methanol In dichloromethane at 20℃; for 24h; Molecular sieve; Inert atmosphere; Schlenk technique; Stage #2: 1-ethylstyrene With 2,2'-{((11bR)-4-hydroxy-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine-2,6-diyl)bis(3,1-phenylene)}bis(9H-thioxanthen-9-one) In 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran at -50℃; for 15h; Inert atmosphere; Schlenk technique; Irradiation; Overall yield = 11.9 mg; stereoselective reaction;
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