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Methyl 5-bromo-2,3-dihydro-1H-indene-2-carboxylate

  • CAS No. 628732-09-2

  • Cat. No. CS-0343617
  • Purity≥95%
  • MDL No.MFCD17926572

*For research and further manufacturing use only, not for direct human use.

Methyl 5-bromo-2,3-dihydro-1H-indene-2-carboxylate|CS-0343617

Structure of 628732-09-2

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General Information

  • CAS No. 628732-09-2
  • Cat. No. CS-0343617
  • Purity ≥95%
  • MDL No. MFCD17926572
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₁BrO₂
  • Molecular Weight None
  • Synonym(s) 1H-Indene-2-carboxylic acid, 5-bromo-2,3-dihydro-, methyl ester
  • SMILES O=C(C1CC2=C(C=C(Br)C=C2)C1)OC

Description

Methyl 5-bromo-2,3-dihydro-1H-indene-2-carboxylate features a brominated indene core with a pendant methyl ester, enabling direct functionalization at the electron-deficient C5 position. This bench-stable scaffold integrates readily into transition-metal-catalyzed coupling cascades and serves as a key intermediate in synthesizing bioactive heterocycles and pharmaceutical analogs.

Application

Methyl 5-bromo-2,3-dihydro-1H-indene-2-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo substituent. The dihydroindene core provides rigidity and spatial control, while the ester functionality allows for further transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for applications in medicinal chemistry and materials science.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   26.3
  • LogP   2.3369
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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