2'-Bromoacetanilide

≥98%

Reagent Code: #146831
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CAS Number 614-76-6

science Other reagents with same CAS 614-76-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.06 g/mol
Formula C₈H₈BrNO
badge Registry Numbers
MDL Number MFCD00099252
thermostat Physical Properties
Melting Point 102°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the formation of more complex aniline derivatives through substitution or coupling reactions. Commonly employed in the development of active pharmaceutical ingredients where bromine acts as a leaving group for nucleophilic attack. Also utilized in research settings for the synthesis of dyes and functionalized aromatic compounds. Its acetyl-protected amine group enhances stability during reaction sequences, allowing selective transformations on the aromatic ring.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿480.00
inventory 25g
10-20 days ฿1,760.00

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2'-Bromoacetanilide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the formation of more complex aniline derivatives through substitution or coupling reactions. Commonly employed in the development of active pharmaceutical ingredients where bromine acts as a leaving group for nucleophilic attack. Also utilized in research settings for the synthesis of dyes and functionalized aromatic compounds. Its acetyl-protected amine gr

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the formation of more complex aniline derivatives through substitution or coupling reactions. Commonly employed in the development of active pharmaceutical ingredients where bromine acts as a leaving group for nucleophilic attack. Also utilized in research settings for the synthesis of dyes and functionalized aromatic compounds. Its acetyl-protected amine group enhances stability during reaction sequences, allowing selective transformations on the aromatic ring.

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