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Chemical Structure| 127510-98-9 Chemical Structure| 127510-98-9

Structure of 127510-98-9

Chemical Structure| 127510-98-9
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Product Details of [ 127510-98-9 ]

CAS No. :127510-98-9
Formula : C10H9NO2
M.W : 175.18
SMILES Code : O=C(C1C(C#N)=CC=CC=1C)OC
MDL No. :MFCD18399109
InChI Key :OVCFEGUYKGFRQT-UHFFFAOYSA-N
Pubchem ID :10058030

Safety of [ 127510-98-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 127510-98-9 ]

* 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 [ 127510-98-9 ]

[ 127510-98-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 127510-98-9 ]
  • [ 1022980-69-3 ]
YieldReaction ConditionsOperation in experiment
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In chloroform; for 18.0h;Heating / reflux; EXAMPLE 6C methyl 2-bromomethyl-6-cyanobenzoate To a solution of EXAMPLE 6B (2.37 g) in chloroform (30 mL) was added N-bromosuccinimide (2.41 g) and AIBN (4 mg), and the mixture was heated at reflux for 18 hours. After cooling, the solvent was removed, and the concentrate was partitioned between ethyl acetate and water. The extract was washed with brine and concentrated, and the concentrate was purified by flash chromatography on silica gel with 20% ethyl acetate in hexanes.
 

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