3-Bromo-5-chloro-N,N-dimethylaniline

95%

Reagent Code: #215280
fingerprint
CAS Number 1369856-72-3

science Other reagents with same CAS 1369856-72-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.52 g/mol
Formula C₈H₉BrClN
badge Registry Numbers
MDL Number MFCD29092535
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of dyes and pigments. It serves as a building block in the development of functional materials, including photochromic and electroactive compounds. Commonly employed in organic synthesis for introducing dimethylamino and halogen functionalities into larger molecules, especially in the creation of advanced intermediates for drug discovery. Its reactivity makes it valuable in cross-coupling reactions, such as Suzuki and Ullmann reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the manufacture of specialty polymers and in research laboratories for designing novel aromatic amines with tailored electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿45,000.00
3-Bromo-5-chloro-N,N-dimethylaniline
No image available

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of dyes and pigments. It serves as a building block in the development of functional materials, including photochromic and electroactive compounds. Commonly employed in organic synthesis for introducing dimethylamino and halogen functionalities into larger molecules, especially in the creation of advanced intermediates for drug discovery. Its reactivity makes it valuable in cross-coupling reactio

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of dyes and pigments. It serves as a building block in the development of functional materials, including photochromic and electroactive compounds. Commonly employed in organic synthesis for introducing dimethylamino and halogen functionalities into larger molecules, especially in the creation of advanced intermediates for drug discovery. Its reactivity makes it valuable in cross-coupling reactions, such as Suzuki and Ullmann reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the manufacture of specialty polymers and in research laboratories for designing novel aromatic amines with tailored electronic properties.

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...