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AC69536

953411-10-4 | 7-Bromo-1h-indazol-5-amine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $18.00 $13.00 -   +
250mg 95% in stock $21.00 $15.00 -   +
1g 95% in stock $22.00 $16.00 -   +

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*All prices are in USD.

Description
Catalog Number: AC69536
Chemical Name: 7-Bromo-1h-indazol-5-amine
CAS Number: 953411-10-4
Molecular Formula: C7H6BrN3
Molecular Weight: 212.0466
MDL Number: MFCD08275114
SMILES: Nc1cc(Br)c2c(c1)cn[nH]2

 

Upstream Synthesis Route
  • The upstream synthesis route for 7-Bromo-1H-indazol-5-amine can be outlined as follows:
    
    1. Start with a readily available starting material such as o-phenylenediamine and react it with a suitable diazo compound to synthesize an indazole scaffold through a Diazo-transfer reaction or Fisher Indole Synthesis.
    
    2. Once the indazole core is synthesized, brominate at the 7-position using N-bromosuccinimide (NBS) in the presence of a radical starter such as azobisisobutyronitrile (AIBN) under appropriate conditions to obtain 7-bromoindazole.
    
    3. The last step involves the introduction of the amine group at the 5-position which can be achieved via nucleophilic substitution of an appropriate leaving group (possibly a nitro or halide group) at the 5-position with an amine source under suitable reaction conditions.
    
    Each step in this synthesis requires careful control of reaction conditions including temperature, pH, and use of protective groups if necessary to ensure the correct regiochemistry and to protect the functional groups that are sensitive or not involved in the current reaction step. The overall yield and purity of 7-Bromo-1H-indazol-5-amine are dependent on the efficiency of each of these steps and the purification methods employed.
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