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CS-W001157 4
Total: USD 88.00

(R)-1-(2-Bromophenyl)ethanol

  • CAS No. 76116-20-6

  • Cat. No. CS-W015573
  • Purity≥98%
  • MDL No.MFCD00216591

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

(R)-1-(2-Bromophenyl)ethanol|CS-W015573

Structure of 76116-20-6

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General Information

  • CAS No. 76116-20-6
  • Cat. No. CS-W015573
  • Purity ≥98%
  • MDL No. MFCD00216591
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₉BrO
  • Molecular Weight 201.06
  • Synonym(s) (R)-2-bromo-alpha-methylbenzyl alcohol
  • SMILES C[C@@H](O)C1=CC=CC=C1Br

Description

(R)-1-(2-Bromophenyl)ethanol is a chiral building block featuring a stereodefined hydroxyl group adjacent to a brominated aromatic ring. This configuration enables selective transformations in asymmetric synthesis, particularly in the construction of enantiopure pharmaceutical intermediates. The molecule exhibits stability under standard handling conditions and integrates readily into transition metal-catalyzed coupling processes.

Application

(R)-1-(2-Bromophenyl)ethanol serves as a chiral building block for asymmetric synthesis, enabling stereoselective transformations in medicinal chemistry and catalytic processes. Its bench-stable nature and well-defined stereochemistry facilitate reliable use in cross-coupling reactions, nucleophilic additions, and the construction of bioactive heterocycles. The bromo group provides a versatile handle for further functionalization via Pd-catalyzed coupling protocols.

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-P405-P501

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Computational Chemistry Data

  • TPSA   20.23
  • LogP   2.5024
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   1

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