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CS-W001157 4
Total: USD 88.00

4-Bromo-5-methyl-3-nitro-1H-pyrazole

  • CAS No. 70951-96-1

  • Cat. No. CS-0042937
  • Purity≥98%
  • MDL No.MFCD01459884
  • HazMat Fee +

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    The shipment is processed through FedEx Ground under the Limited Quantity option.

    Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

    If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

    Type
    HazMat Fee
    Excepted Quantity $0.00
    FedEx Limited Quantities Ground $0.00
    Hazmat Ground shipping $50.00+
    Inaccessible (Haz class 6.1 or 9), Domestic $68.00+
    Accessible (Haz class 3, 4, 5 or 8), Domestic $158.00+
    Inaccessible (Haz class 6.1 or 9), International $108.00+
    Accessible (Haz class 3, 4, 5 or 8), International $238.00+

    An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

    There is a HazMat shipping fee for each item that qualifies as a dangerous good. Please contact our quotation team via email to confirm the details.

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

4-Bromo-5-methyl-3-nitro-1H-pyrazole|CS-0042937

Structure of 70951-96-1

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Description

4-Bromo-5-methyl-3-nitro-1H-pyrazole features a fused heterocyclic core with complementary electron-withdrawing and donor substituents, enabling efficient functionalization in transition metal-catalyzed cross-coupling reactions. The bromine atom serves as a high-reactivity handle for palladium-mediated transformations, while the nitro group enhances electrophilicity at C3. This scaffold demonstrates stability under standard bench conditions and facilitates rapid access to complex nitrogen-containing architectures in medicinal chemistry and materials science applications.

Application

4-Bromo-5-methyl-3-nitro-1H-pyrazole serves as a versatile building block in medicinal chemistry, enabling direct access to substituted pyrazole scaffolds via palladium-catalyzed cross-coupling reactions. The bromo group facilitates efficient C–C bond formation under standard Suzuki or Stille conditions, while the nitro and methyl substituents provide orthogonal functional handles for further derivatization. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for high-throughput synthesis and API intermediate development.

General Information

  • CAS No. 70951-96-1
  • Cat. No. CS-0042937
  • Purity ≥98%
  • MDL No. MFCD01459884
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄H₄BrN₃O₂
  • Molecular Weight 206.00
  • Synonym(s) 4-broMo-5-Methyl-3-nitropyrazole
  • SMILES O=[N+](C1=NNC(C)=C1Br)[O-]

Computational Chemistry Data

  • TPSA   71.82
  • LogP   1.38882
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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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