3-(3-Chlorophenyl)propanoic acid

97 %

Reagent Code: #159935
fingerprint
CAS Number 21640-48-2

science Other reagents with same CAS 21640-48-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.62 g/mol
Formula C₉H₉ClO₂
badge Registry Numbers
MDL Number MFCD00014580
thermostat Physical Properties
Melting Point 72-76°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its aromatic and carboxylic functional groups allow for derivatization into esters, amides, or other bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the chlorophenyl moiety’s influence on lipophilicity and receptor binding. Also utilized in the preparation of specialty chemicals and agrochemicals where substituted phenylpropanoic frameworks are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿790.00
inventory 10g
10-20 days ฿1,460.00
inventory 25g
10-20 days ฿3,320.00
inventory 100g
10-20 days ฿12,070.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(3-Chlorophenyl)propanoic acid
No image available

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its aromatic and carboxylic functional groups allow for derivatization into esters, amides, or other bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the chlorophenyl moiety’s influence on lipophilicity and receptor binding. Also utilized in the preparation of specialty chemicals and agrochemica

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its aromatic and carboxylic functional groups allow for derivatization into esters, amides, or other bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the chlorophenyl moiety’s influence on lipophilicity and receptor binding. Also utilized in the preparation of specialty chemicals and agrochemicals where substituted phenylpropanoic frameworks are required.

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...