N’-Acetyl-2-Bromoacetohydrazide

95%

Reagent Code: #220020
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CAS Number 1342263-70-0

science Other reagents with same CAS 1342263-70-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.01 g/mol
Formula C₄H₇BrN₂O₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It serves in the development of pharmaceuticals due to its ability to participate in cyclization reactions, forming nitrogen- and oxygen-containing rings. Commonly employed in the synthesis of bioactive molecules, including potential antimicrobial and antitumor agents. Its bromo functionality allows for further derivatization through nucleophilic substitution, making it valuable in medicinal chemistry research. Also utilized in the creation of specialized agrochemicals and functional materials where controlled reactivity is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,780.00
N’-Acetyl-2-Bromoacetohydrazide
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Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It serves in the development of pharmaceuticals due to its ability to participate in cyclization reactions, forming nitrogen- and oxygen-containing rings. Commonly employed in the synthesis of bioactive molecules, including potential antimicrobial and antitumor agents. Its bromo functionality allows for further derivatization through nucleophilic substitution, making it valuable in medicinal chemistry

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It serves in the development of pharmaceuticals due to its ability to participate in cyclization reactions, forming nitrogen- and oxygen-containing rings. Commonly employed in the synthesis of bioactive molecules, including potential antimicrobial and antitumor agents. Its bromo functionality allows for further derivatization through nucleophilic substitution, making it valuable in medicinal chemistry research. Also utilized in the creation of specialized agrochemicals and functional materials where controlled reactivity is required.

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