3-Amino-2-bromobenzoic acid

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Reagent Code: #137318
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CAS Number 168899-61-4

science Other reagents with same CAS 168899-61-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.032 g/mol
Formula C₇H₆BrNO₂
badge Registry Numbers
MDL Number MFCD07786957
thermostat Physical Properties
Melting Point 153 - 158 ℃
Boiling Point 367.4 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.793±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of heterocyclic compounds, particularly in the development of active ingredients for herbicides and fungicides. Also employed in the production of dyes and pigments due to its ability to undergo diazotization and coupling reactions. Its amino and carboxylic acid functional groups allow for peptide coupling and derivatization in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿920.00
inventory 5g
10-20 days ฿3,310.00
inventory 25g
10-20 days ฿12,380.00

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3-Amino-2-bromobenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of heterocyclic compounds, particularly in the development of active ingredients for herbicides and fungicides. Also employed in the production of dyes and pigments due to its ability to undergo diazotization and coupling reactions. Its amino and carboxylic acid functional groups allow for peptide coupling and derivatization in medicinal chemistry research.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of heterocyclic compounds, particularly in the development of active ingredients for herbicides and fungicides. Also employed in the production of dyes and pigments due to its ability to undergo diazotization and coupling reactions. Its amino and carboxylic acid functional groups allow for peptide coupling and derivatization in medicinal chemistry research.

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