3,4-Dichloro-2-hydroxybenzaldehyde

95%

Reagent Code: #177215
fingerprint
CAS Number 23602-61-1

science Other reagents with same CAS 23602-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.01 g/mol
Formula C₇H₄Cl₂O₂
badge Registry Numbers
MDL Number MFCD13192524
inventory_2 Storage & Handling
Storage 2-8°C, inert atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain antimicrobial and antifungal agents. It serves as a building block in organic reactions due to the presence of both aldehyde and hydroxyl functional groups, enabling Schiff base formation and ring substitution reactions. Commonly employed in the development of dyes and fragrances where chlorinated aromatic aldehydes contribute to stability and specific olfactory properties. Also utilized in research for designing novel bioactive molecules and coordination compounds with metal ions for catalytic or medicinal applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿30,070.00
inventory 250mg
10-20 days ฿48,570.00
inventory 1g
10-20 days ฿73,940.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3,4-Dichloro-2-hydroxybenzaldehyde
No image available

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain antimicrobial and antifungal agents. It serves as a building block in organic reactions due to the presence of both aldehyde and hydroxyl functional groups, enabling Schiff base formation and ring substitution reactions. Commonly employed in the development of dyes and fragrances where chlorinated aromatic aldehydes contribute to stability and specific olfactory properties. Also utiliz

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain antimicrobial and antifungal agents. It serves as a building block in organic reactions due to the presence of both aldehyde and hydroxyl functional groups, enabling Schiff base formation and ring substitution reactions. Commonly employed in the development of dyes and fragrances where chlorinated aromatic aldehydes contribute to stability and specific olfactory properties. Also utilized in research for designing novel bioactive molecules and coordination compounds with metal ions for catalytic or medicinal applications.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...