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Chemical Structure| 7560-50-1 Chemical Structure| 7560-50-1

Structure of 7560-50-1

Chemical Structure| 7560-50-1

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Product Details of [ 7560-50-1 ]

CAS No. :7560-50-1
Formula : C11H10O3
M.W : 190.20
SMILES Code : O=C(OC)/C=C/C1=CC=C(C=O)C=C1
MDL No. :MFCD00157179
InChI Key :KVXMLLMZXPRPNG-VOTSOKGWSA-N
Pubchem ID :11008713

Safety of [ 7560-50-1 ]

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

Application In Synthesis of [ 7560-50-1 ]

* 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 [ 7560-50-1 ]

[ 7560-50-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 21109-25-1 ]
  • [ 7560-50-1 ]
  • (2E)-3-[4-[[(1H-indol-2-ylmethyl)amino]methyl]phenyl]-2-propenoic acid methyl ester [ No CAS ]
  • 2
  • [ 7560-50-1 ]
  • [ 22259-53-6 ]
  • (2E)-3-(4-[[(1H-indol-3-ylmethyl)amino]methyl]phenyl)propenoic acid methyl ester [ No CAS ]
 

Historical Records

Technical Information

• Acyl Group Substitution • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blanc Chloromethylation • Bouveault-Blanc Reduction • Bucherer-Bergs Reaction • Catalytic Hydrogenation • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Ester Cleavage • Fischer Indole Synthesis • Friedel-Crafts Reaction • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Julia-Kocienski Olefination • Knoevenagel Condensation • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions with Organometallic Reagents • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Stetter Reaction • Stobbe Condensation • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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