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Cat. No.: HY-Y1863

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3-Chlorobenzaldehyde

Name: 3-Chlorobenzaldehyde
Brand: MedChemExpress
SKU: HY-Y1863
Price: 26.00 USD
Availability: InStock
Rating: 5 (1 reviews)

(Synonyms: m-Chlorobenzenecarboxaldehyde)

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3-Chlorobenzaldehyde (m-Chlorobenzenecarboxaldehyde) is a substrate of rat liver microsomal aldehyde dehydrogenase (mALDH) and undergoes mALDH-mediated dehydrogenation to generate the corresponding carboxylic acid. 3-Chlorobenzaldehyde is a chlorine-substituted aromatic benzaldehyde organic synthesis building block and can serve as an intermediate for research related to organic synthesis.

For research use only. We do not sell to patients.

Purity : 98.71%
CAS No.: 587-04-2
Formula: C₇H₅ClO
Molecular Weight:140.57

Storage:

4°C, stored under nitrogen

* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

3-Chlorobenzaldehyde Chemical Structure

CAS No.: 587-04-2

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- IC₅₀ & Target
- In Vitro
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
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Biological Activity

Description

IC₅₀ & Target

IZKF2

In Vitro

3-Chlorobenzaldehyde is a synthetic precursor of monoaromatic ring-substituted aromatic aldehydes and can react with cyclohexanone selenosemicarbazone in an ethanol system, but the desired selenosemicarbazone product cannot be obtained^[1].
3-Chlorobenzaldehyde reacts with 4-bromoacetophenone (HY-20436) to synthesize chalcone JA2, and the resulting JA2 possesses antioxidant and α-glucosidase inhibitory activities^[2].
3-Chlorobenzaldehyde (compound 9) is a substrate of purified rat liver mALDH, with a K_m of 968 µM and a V_max of 20.3 nmol/min (µg/protein)^[3].
3-Chlorobenzaldehyde can react as a precursor to yield Schiff base derivatives^[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

CAS No. 587-04-2
Appearance <9°C Solid,>12°C Liquid
Molecular Weight 140.57
Formula C₇H₅ClO
Color Colorless to light yellow
SMILES

O=CC1=CC(Cl)=CC=C1
Synonyms

m-Chlorobenzenecarboxaldehyde
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

4°C, stored under nitrogen

* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (271 KB)
SDS (394 KB)
- English - EN (394 KB)
- Français - FR (394 KB)
- Deutsch - DE (394 KB)
- Norwegian - NO (394 KB)
- Español - ES (394 KB)
- Swedish - SV (394 KB)
- Italian - IT (394 KB)
- Korean - KR (394 KB)
- Portuguese - PT (394 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Malhi R, et al. Synthesis, characterization and antitubercular activities of heterocyclic selenosemicarbazones. Bioorganic chemistry. 2022 Sep;126:105907.

[2]. Uddin J, et al. Chalcones: The flavonoid derivatives synthesis, characterization, their antioxidant and in vitro/in vivo antidiabetic potentials. Heliyon. 2023 Nov 1;9(11).

[3]. Martini R, et al. Rat hepatic microsomal aldehyde dehydrogenase. Identification of 3- and 4-substituted aromatic aldehydes as substrates of the enzyme. Chemical research in toxicology. 1996;9(1):268-76.

[4]. Karatas H, et al. Alzheimer’s Disease Drug Design by Synthesis, Characterization, Enzyme Inhibition, In Silico, SAR Analysis and MM-GBSA Analysis of Schiff Bases Derivatives: H. Karatas et al. Korean Journal of Chemical Engineering. 2025 Jul;42(8):1793-811.

Calculators

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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