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CS-W001157 4
Total: USD 88.00

1-Bromo-4-cyclopropyl-2-methoxybenzene

  • CAS No. 1353855-71-6

  • Cat. No. CS-0375868
  • Purity≥95%
  • MDL No.None

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

1-Bromo-4-cyclopropyl-2-methoxybenzene|CS-0375868

Structure of 1353855-71-6

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General Information

  • CAS No. 1353855-71-6
  • Cat. No. CS-0375868
  • Purity ≥95%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₁BrO
  • Molecular Weight 227.10
  • Synonym(s) Benzene, 1-bromo-4-cyclopropyl-2-methoxy-
  • SMILES COC1=CC(C2CC2)=CC=C1Br

Description

1-Bromo-4-cyclopropyl-2-methoxybenzene features a cyclopropyl group that imparts unique steric and electronic properties, enhancing its utility in cross-coupling reactions. The methoxy substituent stabilizes electron density at the ortho position, while the bromine serves as a reactive handle for palladium-catalyzed transformations. This compound demonstrates robust stability under standard bench conditions, facilitating efficient integration into synthetic sequences requiring precise functional group placement.

Application

1-Bromo-4-cyclopropyl-2-methoxybenzene serves as a versatile aryl halide building block for palladium-catalyzed cross-coupling reactions, enabling efficient access to biaryl scaffolds. The cyclopropyl group enhances metabolic stability, while the methoxy functionality provides orthogonal reactivity and mild directing effects. Bench-stable and compatible with standard Suzuki, Stille, and Negishi protocols, it facilitates streamlined synthesis of complex functionalized aromatics relevant to 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 : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501

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Computational Chemistry Data

  • TPSA   9.23
  • LogP   3.3351
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   2

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