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Chemical Structure| 135322-16-6 Chemical Structure| 135322-16-6

Structure of 135322-16-6

Chemical Structure| 135322-16-6

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Product Details of [ 135322-16-6 ]

CAS No. :135322-16-6
Formula : C7H13N3O2
M.W : 171.20
SMILES Code : O=C(C1CCN(C(N)=N)CC1)O
MDL No. :MFCD09991899
InChI Key :DCYAOXOBKROXKE-UHFFFAOYSA-N
Pubchem ID :5152314

Safety of [ 135322-16-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 135322-16-6 ]

* 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 [ 135322-16-6 ]

[ 135322-16-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 498-94-2 ]
  • [ 1184-90-3 ]
  • [ 135322-16-6 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In water; D. To a solution of 1 g of isonipecotic acid in 10 ml of water was added 1.07 g potassium carbonate and this was stirred for 15 minutes at room temperature. 0.961 g <strong>[1184-90-3]aminoiminomethanesulfonic acid</strong> was then added portionwise over 20 minutes. The solution was stirred for 2 hours at room temperature, concentrated in vacuo to one-half of the original volume and the resulting precipitate collected by filtration. The resulting solid wasrecrystallized from water to give N-amidino-4-piperidine carboxylic acid.
With potassium carbonate; In water; A. N-amidino-4-piperidine carboxylic acid was prepared essentially by the method of Miller, et al, Synthesis, 777 (1986), which is incorporated herein by reference. To a solution of 1 g of isonipecotic acid in 10 ml of water was added 1.07 g potassium carbonate and this was stirred for 15 minutes at room temperature. 0.961 g <strong>[1184-90-3]aminoiminomethanesulfonic acid</strong> was then added portionwise over 20 minutes. The solution was stirred for 2 hours at room temperature, concentrated in vacuo to one-half of the original volume and the resulting precipitate collected by filtration. The resulting solid was recrystallized from water to give N-amidino-4-piperidine carboxylic acid. This was dissolved in an aqueous solution of tetrahydrofuran.
 

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