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Chemical Structure| 617-79-8 Chemical Structure| 617-79-8

Structure of 617-79-8

Chemical Structure| 617-79-8

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Product Details of [ 617-79-8 ]

CAS No. :617-79-8
Formula : C6H15N
M.W : 101.19
SMILES Code : CCC(CN)CC
MDL No. :MFCD00040755
InChI Key :MGWAGIQQTULHGU-UHFFFAOYSA-N
Pubchem ID :12049

Safety of [ 617-79-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H314-H331
Precautionary Statements:P210-P235-P240-P241-P242-P243-P260-P264-P270-P271-P280-P301+P312-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P311-P312-P321-P322-P330-P363-P370+P378-P403+P233-P403+P235-P405-P501
Class:3(6.1,8)
UN#:3286
Packing Group:

Application In Synthesis of [ 617-79-8 ]

* 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 [ 617-79-8 ]

[ 617-79-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 617-79-8 ]
  • [ 1187487-23-5 ]
  • [ 125238-99-5 ]
  • [ 1185654-07-2 ]
YieldReaction ConditionsOperation in experiment
46% Example 33 - Synthesis of Compound 28 (S)-9-fluorenylmethyl 10-(2-ethylbutyl)-2,2- dimethyl-18-phenyl-4,9,13,16-tetraoxo-3,17-dioxa-5,10,15-triazaoctadecan-8- ylcarbamate28(lSr)-9-fluorenylmethyl 10-(2-ethylbutyl)-2,2-dimethyl-18-phenyl- 4,9,13,16-tetraoxo-3,17-dioxa-5,10,15-triazaoctadecan-8- ylcarbamateTo 2-ethylbutylamine (0.15 g, 1.48 mmol) in DCM (10 mL) was added the alpha,beta- unsaturated ketone 15 (1.47 mmol) in DCM (30 mL). After stirring at room temperature for 15 mins, Fmoc-diaminobutyric acid(Boc)-OH (0.95 g, 2.16 mmol) and DIC (0.34 mL, 2.19 mmol) were added. The reaction was stirred at room temperature overnight. The DCM was removed by rotary evaporation and the residue was subjected to column chromatography on silica gel using petroleum spirit:EtOAc (1 :1 to 0:1 ), providing Compound 28 (0.5 g, 46percent).
46% To 2-ethylbutylamine (0.15 g, 1.48 mmol) in DCM (10 mL) was added the alpha,beta-unsaturated ketone 15 (1.47 mmol) in DCM (30 mL).After stirring at room temperature for 15 mins, Fmoc-diaminobutyric acid(Boc)-OH (0.95 g, 2.16 mmol) and DIC (0.34 mL, 2.19 mmol) were added.The reaction was stirred at room temperature overnight.The DCM was removed by rotary evaporation and the residue was subjected to column chromatography on silica gel using petroleum spirit:EtOAc (1:1 to 0:1), providing Compound 28 (0.5 g, 46percent).
  • 2
  • [ 617-79-8 ]
  • [ 2799-07-7 ]
  • [ 81-30-1 ]
  • [ 1283599-73-4 ]
  • 3
  • [ 617-79-8 ]
  • [ 35344-95-7 ]
  • C10H17N3 [ No CAS ]
 

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