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Chemical Structure| 101327-84-8 Chemical Structure| 101327-84-8

Structure of 1-Nitro-2-naphthaldehyde
CAS No.: 101327-84-8

Chemical Structure| 101327-84-8

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Product Details of [ 101327-84-8 ]

CAS No. :101327-84-8
Formula : C11H7NO3
M.W : 201.18
SMILES Code : O=CC1=CC=C2C=CC=CC2=C1[N+]([O-])=O
MDL No. :MFCD03427164
InChI Key :XQIMHJNMEFIADP-UHFFFAOYSA-N
Pubchem ID :4576022

Safety of [ 101327-84-8 ]

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

Application In Synthesis of [ 101327-84-8 ]

* 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 [ 101327-84-8 ]

[ 101327-84-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 101327-84-8 ]
  • [ 78364-55-3 ]
  • 6-fluoro-2-(2-(1-nitronaphthalen-2-ylmethylene)hydrazino)benzothiazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% With acetic acid; In ethanol; at 80℃; for 0.166667h;Microwave irradiation; General procedure: A mixture of compound 2 (0.0549 g, 0.0003 mol), the appropriate aromatic aldehyde (0.00033 mol) and glacial acetic acid (0.1 mL) in ethanol (5 mL) was heated under microwave (20 W) at 80 °C for 10 min. On cooling, the precipitated solid was collected by filtration, washed with water, dried and crystallized to give compounds 3-29.
  • 2
  • [ 22600-30-2 ]
  • [ 101327-84-8 ]
  • methyl 9-hydroxy-7-oxo-7,9-dihydrobenzo[h]pyrrolo[2,1-b]quinazoline-9-carboxylate [ No CAS ]
  • 3
  • [ 22600-30-2 ]
  • [ 101327-84-8 ]
  • C17H12N2O5 [ No CAS ]
 

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