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CS-W001157 4
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Methyl 4-bromo-2-nitrobenzoate

  • CAS No. 158580-57-5

  • Cat. No. CS-W022847
  • Purity≥98%
  • MDL No.MFCD10699645

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

Methyl 4-bromo-2-nitrobenzoate|CS-W022847

Structure of 158580-57-5

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General Information

  • CAS No. 158580-57-5
  • Cat. No. CS-W022847
  • Purity ≥98%
  • MDL No. MFCD10699645
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₆BrNO₄
  • Molecular Weight 260.04
  • Synonym(s) Benzoic acid, 4-bromo-2-nitro-, methyl ester
  • SMILES O=C(OC)C1=CC=C(Br)C=C1[N+]([O-])=O

Description

Methyl 4-bromo-2-nitrobenzoate features a bromine atom at the para position relative to the ester group and a nitro substituent at the ortho position, creating a highly electron-deficient aromatic scaffold. This combination enables selective cross-coupling reactions under palladium catalysis, delivering complex substituted benzoates with high regiocontrol. The molecule exhibits excellent stability under standard bench conditions and integrates seamlessly into synthetic sequences requiring orthogonal functionalization.

Application

Methyl 4-bromo-2-nitrobenzoate serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo group. The nitro functionality provides a handle for selective reduction and subsequent functionalization, while the ester group offers compatibility with standard deprotection and transformation protocols. Its bench-stable nature and predictable reactivity make it well-suited for multi-step synthesis of heterocyclic scaffolds and pharmaceutical intermediates.

Safety Information

Download SDS
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   69.44
  • LogP   2.1439
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   2

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