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Type HazMat fee for 500 gram (Estimated)
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Chemical Structure| 42287-37-6 Chemical Structure| 42287-37-6

Structure of 42287-37-6

Chemical Structure| 42287-37-6

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Product Details of [ 42287-37-6 ]

CAS No. :42287-37-6
Formula : C4H12N2O
M.W : 104.15
SMILES Code : CC(O)(C)CNN
MDL No. :MFCD12764863

Safety of [ 42287-37-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H315-H319
Precautionary Statements:P501-P270-P264-P280-P337+P313-P301+P310+P330
Class:6.1
UN#:2810
Packing Group:

Application In Synthesis of [ 42287-37-6 ]

* 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 [ 42287-37-6 ]

[ 42287-37-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 558-42-9 ]
  • [ 42287-37-6 ]
YieldReaction ConditionsOperation in experiment
1.98 g With hydrazine hydrate; In ethanol;Reflux; A mixture of 1a (20.0 g, 400.0 mmol) and 1b (2.17 g, 20.0 mmol) in ethanol (50 mL) was refluxed overnight, then evaporated under high vacuum. The residue was dissolved in ethanol and the resulting solid was filtered off. The filtrate was concentrated to give crude 1c (1.98 g, 95percent) which was used directly for the next step.
With hydrazine hydrate; sodium hydroxide; at 95℃; Step 1: Intermediate 48-b To a mixture of sodium hydroxide (7.37 g, 184.0 mmol) and hydrazine monohydrate (46.10 g, 921.0 mmol) heated to 95°C, was added l-chloro-2- methylpropan-2-ol (20.00 g, 184.0 mmol). The reaction was stirred overnight at 95 °C and then cooled to room temperature. Volatiles were removed under reduced pressure. THF (40 mL) and diethyl ether (40 mL) were added to the residue; a precipitate formed which was removed by filtration. The filtrate was concentrated under reduced pressure to provide intermediate 48-b as a colorless oil.
  • 2
  • [ 558-42-9 ]
  • [ 302-01-2 ]
  • [ 42287-37-6 ]
YieldReaction ConditionsOperation in experiment
In ethanol;Reflux; Step 1 : A mixture of 5b and 5a in ethanol (50mL) was refluxed overnight, evaporated under high vacuum. The residue was re-dissolved in ethanol and the resulting precipitate was filtered off. The filtrate was concentrated and dried to give crude 5c. The procedure from 5c to 5d was similar to that of Example 1 (1.84g, 61percent from 5a).
 

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