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CS-W001157 4
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7-Bromo-2,2-dimethyl-3H-chromen-4-one

  • CAS No. 130200-01-0

  • Cat. No. CS-0061116
  • Purity≥98%
  • MDL No.None

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

7-Bromo-2,2-dimethyl-3H-chromen-4-one|CS-0061116

Structure of 130200-01-0

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General Information

  • CAS No. 130200-01-0
  • Cat. No. CS-0061116
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₁BrO₂
  • Molecular Weight 255.11
  • Synonym(s) 7-BROMO-2,3-DIHYDRO-2,2-DIMETHYLCHROMEN-4-ONE
  • SMILES CC1(C)CC(=O)C2=C(C=C(C=C2)Br)O1

Description

7-Bromo-2,2-dimethyl-3H-chromen-4-one features a brominated coumarin core with a sterically shielded dimethyl-substituted C2 position, enhancing stability and modulating electronic properties. This scaffold integrates readily into synthetic routes for bioactive molecules, leveraging its electron-deficient benzene ring and reactive carbonyl group for efficient coupling reactions under standard conditions.

Application

7-Bromo-2,2-dimethyl-3H-chromen-4-one serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted coumarin scaffolds. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the 2,2-dimethyl substitution enhances bench stability and simplifies purification. The molecule functions effectively in heterocyclic synthesis and as a key intermediate in the development of bioactive compounds requiring a sterically protected chromenone core.

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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   26.3
  • LogP   3.1929
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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