Ethyl 4-(1-Hydrazinylethyl)Benzoate Benzenesulfonate

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Reagent Code: #185503
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CAS Number 1415565-11-5

science Other reagents with same CAS 1415565-11-5

blur_circular Chemical Specifications

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Weight 366.43 g/mol
Formula C₁₇H₂₂N₂O₅S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of hydrazine-based pharmaceuticals and bioactive compounds. Its hydrazine functionality allows for coupling reactions in the development of heterocyclic systems, which are common in medicinal chemistry. Commonly employed in research settings for modifying ester and sulfonate-containing molecules to enhance solubility or reactivity. Also utilized in the synthesis of selective enzyme inhibitors and antimicrobial agents due to its ability to form stable derivatives with carbonyl and carboxyl groups.

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inventory 100mg
10-20 days ฿9,750.00

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Ethyl 4-(1-Hydrazinylethyl)Benzoate Benzenesulfonate
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Used as an intermediate in organic synthesis, particularly in the preparation of hydrazine-based pharmaceuticals and bioactive compounds. Its hydrazine functionality allows for coupling reactions in the development of heterocyclic systems, which are common in medicinal chemistry. Commonly employed in research settings for modifying ester and sulfonate-containing molecules to enhance solubility or reactivity. Also utilized in the synthesis of selective enzyme inhibitors and antimicrobial agents due to its

Used as an intermediate in organic synthesis, particularly in the preparation of hydrazine-based pharmaceuticals and bioactive compounds. Its hydrazine functionality allows for coupling reactions in the development of heterocyclic systems, which are common in medicinal chemistry. Commonly employed in research settings for modifying ester and sulfonate-containing molecules to enhance solubility or reactivity. Also utilized in the synthesis of selective enzyme inhibitors and antimicrobial agents due to its ability to form stable derivatives with carbonyl and carboxyl groups.

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