(5-(Methylsulfonyl)pyridin-2-yl)methanamine hydrochloride

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Reagent Code: #209060
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CAS Number 848141-14-0

science Other reagents with same CAS 848141-14-0

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Weight 222.69 g/mol
Formula C₇H₁₁ClN₂O₂S
badge Registry Numbers
MDL Number MFCD26395890
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the sulfone and amine functionalities, which improve solubility and pharmacokinetic properties. Also utilized in research settings for generating analogs in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,800.00
inventory 250mg
10-20 days ฿13,600.00
inventory 1g
10-20 days ฿30,600.00

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(5-(Methylsulfonyl)pyridin-2-yl)methanamine hydrochloride
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the sulfone and amine functionalities, which improve solubility and pharmacokinetic properties. Also utilized in research settings for generating analogs in structure-activity relationship
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Commonly employed in medicinal chemistry for constructing bioactive molecules due to the sulfone and amine functionalities, which improve solubility and pharmacokinetic properties. Also utilized in research settings for generating analogs in structure-activity relationship (SAR) studies.
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