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Chemical Structure| 29704-38-9 Chemical Structure| 29704-38-9

Structure of 29704-38-9

Chemical Structure| 29704-38-9

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Product Details of [ 29704-38-9 ]

CAS No. :29704-38-9
Formula : C12H15NO4
M.W : 237.25
SMILES Code : O=C(OC(C)(C)C)CC1=CC=C([N+]([O-])=O)C=C1
MDL No. :MFCD24943244
Boiling Point : No data available
InChI Key :DQXJXWHNSVKMAT-UHFFFAOYSA-N
Pubchem ID :349070

Safety of [ 29704-38-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P210-P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501

Application In Synthesis of [ 29704-38-9 ]

* 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 [ 29704-38-9 ]

[ 29704-38-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 29704-38-9 ]
  • [ 174579-31-8 ]
YieldReaction ConditionsOperation in experiment
51% With palladium 10% on activated carbon; hydrogen; In methanol; for 3h; Compound 2- (4-nitrophenyl) t-butyl acetate 55b (5 g, 21 mmol) was dissolved in methanol (30 mL),Then 10% palladium on carbon (1 g) was added and stirred for 3 hours under a hydrogen atmosphere.After the reaction was completed, the filtrate was filtered, and the solvent was removed under reduced pressure.The target product tert-butyl 2- (4-aminophenyl) acetate 55c (2.25 g, yellow oil) was obtained in a yield of 51%.
 

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