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Chemical Structure| 128740-03-4 Chemical Structure| 128740-03-4

Structure of 128740-03-4

Chemical Structure| 128740-03-4

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Product Details of [ 128740-03-4 ]

CAS No. :128740-03-4
Formula : C8H13NO3
M.W : 171.19
SMILES Code : O=C(OCC)N(CC=C)CC=O
MDL No. :MFCD09953121
InChI Key :IQQODTFRDRREIO-UHFFFAOYSA-N
Pubchem ID :11084330

Safety of [ 128740-03-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P261-P280-P305+P351+P338-P304+P340-P405-P501

Application In Synthesis of [ 128740-03-4 ]

* 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 [ 128740-03-4 ]

[ 128740-03-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 600-21-5 ]
  • [ 128740-03-4 ]
  • [ 132414-87-0 ]
YieldReaction ConditionsOperation in experiment
In toluene; a) Ethyl 2,3-dimethyl-2,7-diazabicyclo[3.3.0]octane-7-carboxylate STR33 17.2 g (0.1 mol) of ethyl N-allyl-N-(2-oxoethyl) -carbamate are heated under reflux overnight with 10.5 g (0.1 mol) of <strong>[600-21-5]N-methylalanine</strong> in 300 ml of toluene. The mixture is concentrated and the residue is distilled. Yield: 11.3 g (53.2% of theory). Boiling point: 81 C./0.25 mbar.
 

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Technical Information

• Acyl Group Substitution • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bouveault-Blanc Reduction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Catalytic Hydrogenation • Chan-Lam Coupling Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Ester Cleavage • Fischer Indole Synthesis • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Heat of Combustion • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Julia-Kocienski Olefination • Knoevenagel Condensation • Lawesson's Reagent • Leuckart-Wallach Reaction • Mannich 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 Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions with Organometallic Reagents • Reformatsky Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • Stetter Reaction • Stobbe Condensation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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