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CS-W001157 4
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1H-Benzo[d]imidazole-2-carbaldehyde

  • CAS No. 3314-30-5

  • Cat. No. CS-W004873
  • Purity≥95%
  • MDL No.MFCD00228045
  • HazMat Fee +

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    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.

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

1H-Benzo[d]imidazole-2-carbaldehyde|CS-W004873

Structure of 3314-30-5

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Description

1H-Benzo[d]imidazole-2-carbaldehyde features a rigid heteroaromatic core with a reactive aldehyde group at the 2-position, enabling direct incorporation into diverse molecular architectures. This bench-stable compound serves as a key scaffold for synthesizing bioactive imidazoles, ligands, and functional materials through efficient condensation or coupling reactions under standard conditions.

Application

1H-Benzo[d]imidazole-2-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its aldehyde functionality facilitates nucleophilic addition, reductive amination, and Ugi-type coupling reactions with high reliability. The molecule exhibits excellent bench stability and compatibility with common functional groups, supporting straightforward purification and integration into multi-step synthetic sequences.

General Information

  • CAS No. 3314-30-5
  • Cat. No. CS-W004873
  • Purity ≥95%
  • MDL No. MFCD00228045
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₆N₂O
  • Molecular Weight 146.15
  • Synonym(s) 1H-Benzimidazole-2-carboxaldehyde
  • SMILES O=CC1=NC2=CC=CC=C2N1

Computational Chemistry Data

  • TPSA   45.75
  • LogP   1.3754
  • H_Acceptors   2
  • 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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