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CS-W001157 4
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3-Bromo-5-chloro-2-hydroxybenzaldehyde

  • CAS No. 19652-32-5

  • Cat. No. CS-W010326
  • Purity≥98%
  • MDL No.MFCD00051690
  • 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.

3-Bromo-5-chloro-2-hydroxybenzaldehyde|CS-W010326

Structure of 19652-32-5

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Description

N-Fmoc-L-alanine is potentially useful for proteomics studies and solid phase peptide synthesis techniques. Alanine is one of the simplest amino acids - a methyl group as the side chain. This small side chain confers a high degree of flexibility when incorporated into a polypeptide chain. The Fmoc group is typically removed with a base such as pyridine - an orthogonal de-protection strategy to the acid labilie Boc group.

Application

3-Bromo-5-chloro-2-hydroxybenzaldehyde serves as a versatile building block for the synthesis of substituted benzene derivatives and heterocyclic scaffolds. Its strategic placement of bromo, chloro, and hydroxy groups enables selective functionalization via cross-coupling, electrophilic substitution, or protection strategies. The aldehyde functionality facilitates condensation reactions, while the phenolic hydroxyl group offers opportunities for derivatization or metal coordination. Bench-stable and compatible with standard purification methods, it supports efficient workflow integration in medicinal chemistry and materials science applications.

General Information

  • CAS No. 19652-32-5
  • Cat. No. CS-W010326
  • Purity ≥98%
  • MDL No. MFCD00051690
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄BrClO₂
  • Molecular Weight 235.46
  • Synonym(s) 3-Bromo-5-chlorosalicylaldehyde; 3-Bromo-5-chloro-2-hydroxybenzaldehyde
  • SMILES O=CC1=CC(Cl)=CC(Br)=C1O

Computational Chemistry Data

  • TPSA   37.3
  • LogP   2.6206
  • 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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