4,5-Dichloro-N1-isobutylbenzene-1,2-diamine hydrochloride

98%

Reagent Code: #169119
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CAS Number 957035-41-5

science Other reagents with same CAS 957035-41-5

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Weight 269.60 g/mol
Formula C₁₀H₁₅Cl₃N₂
badge Registry Numbers
MDL Number MFCD09475890
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Storage Room temperature

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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures when reacted with carbonyl compounds. Commonly employed in the preparation of imidazoles and other nitrogen-containing rings that exhibit biological activity. Also utilized in research settings for structure-activity relationship (SAR) studies targeting inflammatory and neurodegenerative diseases. Its chloro and amine functionalities allow for selective modifications, enabling fine-tuning of molecular properties in drug design.

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inventory 100mg
10-20 days ฿13,440.00

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4,5-Dichloro-N1-isobutylbenzene-1,2-diamine hydrochloride
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures when reacted with carbonyl compounds. Commonly employed in the preparation of imidazoles and other nitrogen-containing rings that exhibit biological activity. Also utilized in research settings for structure-activity relationship (SAR) studies targeting

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures when reacted with carbonyl compounds. Commonly employed in the preparation of imidazoles and other nitrogen-containing rings that exhibit biological activity. Also utilized in research settings for structure-activity relationship (SAR) studies targeting inflammatory and neurodegenerative diseases. Its chloro and amine functionalities allow for selective modifications, enabling fine-tuning of molecular properties in drug design.

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