4-Bromo-3-methylbenzoic acid

98%

Reagent Code: #143439
label
Alias 4-Bromotoluene acid 3-methyl-4-bromobenzoic acid
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CAS Number 7697-28-1

science Other reagents with same CAS 7697-28-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.04 g/mol
Formula C₈H₇BrO₂
badge Registry Numbers
EC Number 231-713-7
MDL Number MFCD00039526
thermostat Physical Properties
Melting Point 212-216 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its functional groups allow for further chemical modifications, making it valuable in creating active ingredients in drug development. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex aromatic structures. Also utilized in the preparation of liquid crystals and organic electronic materials due to its stable aromatic backbone and substituent positioning.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿144.00
5g
10-20 days ฿270.00
25g
10-20 days ฿700.00
100g
10-20 days ฿2,510.00
4-Bromo-3-methylbenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its functional groups allow for further chemical modifications, making it valuable in creating active ingredients in drug development. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex aromatic structures. Also utilized in the preparation of liquid crystals and organic electronic materials due to its stable aromatic backbone and substituent positioning.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its functional groups allow for further chemical modifications, making it valuable in creating active ingredients in drug development. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build complex aromatic structures. Also utilized in the preparation of liquid crystals and organic electronic materials due to its stable aromatic backbone and substituent positioning.

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