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[ CAS No. 51707-35-8 ] {[proInfo.proName]}

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Chemical Structure| 51707-35-8
Chemical Structure| 51707-35-8
Structure of 51707-35-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 51707-35-8 ]

CAS No. :51707-35-8 MDL No. :MFCD00122691
Formula : C8H10N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 166.18 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 51707-35-8 ]

* 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 [ 51707-35-8 ]

[ 51707-35-8 ] Synthesis Path-Downstream   1~24

  • 1
  • [ 98-01-1 ]
  • [ 51707-35-8 ]
  • furfural-(2-hydroxymethyl-benzoylhydrazone) [ No CAS ]
  • 2
  • [ 620-02-0 ]
  • [ 51707-35-8 ]
  • 2-hydroxymethyl-benzoic acid-(5-methyl-furfurylidenehydrazide) [ No CAS ]
  • 3
  • [ 67-47-0 ]
  • [ 51707-35-8 ]
  • 5-hydroxymethyl-furan-2-carbaldehyde-(2-hydroxymethyl-benzoylhydrazone) [ No CAS ]
  • 4
  • [ 87-41-2 ]
  • [ 51707-35-8 ]
YieldReaction ConditionsOperation in experiment
With ethanol; hydrazine hydrate
With water; hydrazine hydrate
  • 5
  • [ 120-57-0 ]
  • [ 51707-35-8 ]
  • piperonal-(2-hydroxymethyl-benzoylhydrazone) [ No CAS ]
  • 6
  • [ 3458-28-4 ]
  • [ 51707-35-8 ]
  • 2-hydroxymethyl-benzoic acid D-mannitol-1-ylidenehydrazide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With ethanol
  • 8
  • [ 51707-35-8 ]
  • [ 108-24-7 ]
  • <i>N</i>-acetyl-<i>N</i>'-(2-hydroxymethyl-benzoyl)-hydrazine [ No CAS ]
  • 9
  • [ 51707-35-8 ]
  • [ 104-88-1 ]
  • 2-hydroxymethyl-benzoic acid-(4-chloro-benzylidenehydrazide) [ No CAS ]
  • 10
  • [ 51707-35-8 ]
  • [ 89-98-5 ]
  • 2-hydroxymethyl-benzoic acid-(3-chloro-benzylidenehydrazide) [ No CAS ]
  • 11
  • [ 51707-35-8 ]
  • [ 99-61-6 ]
  • 2-hydroxymethyl-benzoic acid-(3-nitro-benzylidenehydrazide) [ No CAS ]
  • 12
  • [ 51707-35-8 ]
  • [ 555-16-8 ]
  • 2-hydroxymethyl-benzoic acid-(4-nitro-benzylidenehydrazide) [ No CAS ]
  • 13
  • [ 51707-35-8 ]
  • [ 100-52-7 ]
  • 2-hydroxymethyl-benzoic acid benzylidenehydrazide [ No CAS ]
  • 14
  • [ 51707-35-8 ]
  • [ 123-11-5 ]
  • 2-hydroxymethyl-benzoic acid-(4-methoxy-benzylidenehydrazide) [ No CAS ]
YieldReaction ConditionsOperation in experiment
With ethanol
  • 15
  • [ 51707-35-8 ]
  • [ 587-04-2 ]
  • 2-hydroxymethyl-benzoic acid-(2-chloro-benzylidenehydrazide) [ No CAS ]
  • 16
  • [ 51707-35-8 ]
  • [ 67-64-1 ]
  • 2-hydroxymethyl-benzoic acid isopropylidenehydrazide [ No CAS ]
  • 17
  • [ 51707-35-8 ]
  • [ 119-67-5 ]
  • 2-[(2-hydroxymethyl-benzoylhydrazono)-methyl]-benzoic acid [ No CAS ]
  • 18
  • [ 51707-35-8 ]
  • [ 552-89-6 ]
  • 2-hydroxymethyl-benzoic acid-(2-nitro-benzylidenehydrazide) [ No CAS ]
  • 19
  • [ 87-41-2 ]
  • [ 64-17-5 ]
  • [ 7803-57-8 ]
  • [ 51707-35-8 ]
  • 20
  • [ 51707-35-8 ]
  • [ 302-01-2 ]
  • 21
  • [ 41150-46-3 ]
  • [ 51707-35-8 ]
YieldReaction ConditionsOperation in experiment
70% With hydrazine hydrate In methanol for 48h; Preparation of hydrazide: A typical procedure 1 General procedure: A solution of methyl 4-tert-butylbenzoate (5.15 g, 26.8 mmol) and hydrazine monohydrate (1.50 ml, 30.0 mmol) in MeOH (15 mL) was stirred for 2 d. After the removal of the solvent in vacuo, the residue was recrystallized from MeOH to give 4-tert-butylbenzohydrazide (1b) (2.94 g, 15.3 mmol, 57%) as a colorless crystal. 1 H-NMR (300 MHz, DMSO-d 6 ): δ 9.68 (s, 1H), 7.75 (d, J = 8.5 Hz, 2H), 7.45 (d, J = 8.5 Hz, 2H), 4.44 (s, 2H), 1.28 (s, 9H) ppm.
  • 22
  • [ 51707-35-8 ]
  • [ 87-41-2 ]
YieldReaction ConditionsOperation in experiment
97% With t-butyldimethylsiyl triflate; N,N-dimethyl-formamide at 20℃; for 20h;
  • 23
  • [ 69739-34-0 ]
  • [ 51707-35-8 ]
  • [ 33513-42-7 ]
  • C15H24N2O3Si [ No CAS ]
YieldReaction ConditionsOperation in experiment
63% With 1H-imidazole at 20℃; for 24h; N-Formylation of aminoalcohol: A general procedure General procedure: To a solution of 5 (1.0 mmol) in DMF (1.0 mL), TBSOTf (2.0 mmol) and imidazole (1.0 mmol) were added at room temperature. After stirring for 24 h, the volatiles were evacuated, and the residue was directly chromatographed (eluent: dichloromethane:methanol, 20:1, v/v) to obtain 6.
  • 24
  • [ 51707-35-8 ]
  • [ 18162-48-6 ]
  • [ 33513-42-7 ]
  • C15H24N2O3Si [ No CAS ]
YieldReaction ConditionsOperation in experiment
52% With 1H-imidazole at 20℃; for 24h;
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