3-bromonaphthalene-2-carboxylicacid

98%

Reagent Code: #155560
fingerprint
CAS Number 20717-80-0

science Other reagents with same CAS 20717-80-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.08 g/mol
Formula C₁₁H₇BrO₂
badge Registry Numbers
MDL Number MFCD00089977
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization in the development of complex polycyclic compounds. Commonly employed in coupling reactions to form biaryl systems, which are important in drug discovery. Also utilized in the synthesis of fluorescent dyes and organic semiconductors due to the naphthalene backbone’s electronic properties. The bromine atom facilitates cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in building molecular complexity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,810.00
inventory 250mg
10-20 days ฿11,550.00
inventory 1g
10-20 days ฿31,150.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-bromonaphthalene-2-carboxylicacid
No image available

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization in the development of complex polycyclic compounds. Commonly employed in coupling reactions to form biaryl systems, which are important in drug discovery. Also utilized in the synthesis of fluorescent dyes and organic semiconductors due to the naphthalene backbone’s electronic properties. The bromine atom facilitates cross-coupling reactions such a

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization in the development of complex polycyclic compounds. Commonly employed in coupling reactions to form biaryl systems, which are important in drug discovery. Also utilized in the synthesis of fluorescent dyes and organic semiconductors due to the naphthalene backbone’s electronic properties. The bromine atom facilitates cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in building molecular complexity.

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...