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[ CAS No. 62214-39-5 ]

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2D
Chemical Structure| 62214-39-5
Chemical Structure| 62214-39-5
Structure of 62214-39-5 *Storage: {[proInfo.prStorage]}

Quality Control of [ 62214-39-5 ]

Related Doc. of [ 62214-39-5 ]

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Alternatived Products of [ 62214-39-5 ]
Alternatived Products of [ 62214-39-5 ]

Product Details of [ 62214-39-5 ]

CAS No. :62214-39-5MDL No. :MFCD00145261
Formula : C4H8O2 Boiling Point : -
Linear Structure Formula :-InChI Key :-
M.W :88.11Pubchem ID :-
Synonyms :

Computed Properties of [ 62214-39-5 ]

TPSA : - H-Bond Acceptor Count : -
XLogP3 : - H-Bond Donor Count : -
SP3 : - Rotatable Bond Count : -

Safety of [ 62214-39-5 ]

Signal Word:WarningClass:
Precautionary Statements:P261-P305+P351+P338UN#:
Hazard Statements:H315-H319-H335Packing Group:
GHS Pictogram:

Application In Synthesis of [ 62214-39-5 ]

  • Downstream synthetic route of [ 62214-39-5 ]

[ 62214-39-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 106-99-0 ]
  • [ 62214-39-5 ]
  • [ 86106-09-4 ]
  • [ 5077-67-8 ]
  • 2
  • [ 62214-39-5 ]
  • [ 52642-66-7 ]
  • [ 5077-67-8 ]
  • 3
  • [ 62214-39-5 ]
  • [ 73522-17-5 ]
YieldReaction ConditionsOperation in experiment
68% In palladium-carbon; ethanol; a. Preparation of (2S)-1,2,-butanediol A solution of (2S)-3-butene-1,2-diol which was purchased from Eastman Kodak, (3 g, 0.034 mmoles) in 40 mL of ethanol was hydrogenated in the presence of 300 mg of 10% Pd/C overnight. The so-formed reaction mixture was filtered through celite. The so-formed filter cake was washed with ethanol and the combined filtrates were evaporated to provide 2.08 g (68% yield) of the title compound.
68% In palladium-carbon; ethanol; EXAMPLE 23 STR51 a. Preparation of (2S)-1,2-butanediol A solution of (2S)-3-butene-1,2-diol which was purchased from Eastman Kodak, (3 g, 0.034mmoles) in 40 mL of ethanol was hydrogenated in the presence of 300 mg of 10% Pd/C overnight. The so-formed reaction mixture was filtered through celite. The so-formed filter cake was washed with ethanol and the combined filtrates were evaporated to provide 2.08 g (68% yield) of the title compound.
  • 4
  • [ 62214-39-5 ]
  • [ 584-03-2 ]
YieldReaction ConditionsOperation in experiment
68% In palladium-carbon; ethanol 30.a a. a. Preparation of (2S)-1,2,butanediol A solution of (2S)-3-butene-1,2-diol which was purchased from Eastman Kodak, (3 g, 0.034 mmoles) in 40 mL of ethanol was hydrogenated in the presence of 300 mg of 10% Pd/C overnight. The so-formed reaction mixture was filtered through celite. The so-formed filter cake was washed with ethanol and the combined filtrates were evaporated to provide 2.08 g (68% yield) of the title compound.
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