(S)-Methyl hexahydropyridazine-3-carboxylate hydrochloride

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Reagent Code: #236951
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CAS Number 380223-17-6

science Other reagents with same CAS 380223-17-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.63 g/mol
Formula C₆H₁₃ClN₂O₂
badge Registry Numbers
MDL Number MFCD33019683
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports the formation of nitrogen-containing heterocycles, which are common in medicinal chemistry. The compound is valuable in asymmetric synthesis due to its stereochemical purity, enabling the production of enantiomerically enriched intermediates. It has been employed in research toward central nervous system agents and enzyme inhibitors. Its hydrochloride salt form enhances stability and solubility, facilitating handling in synthetic routes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,190.00
250mg
10-20 days ฿2,530.00
500mg
10-20 days ฿4,370.00
1g
10-20 days ฿7,410.00
5g
10-20 days ฿25,920.00
25g
10-20 days ฿100,390.00
(S)-Methyl hexahydropyridazine-3-carboxylate hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports the formation of nitrogen-containing heterocycles, which are common in medicinal chemistry. The compound is valuable in asymmetric synthesis due to its stereochemical purity, enabling the production of enantiomerically enriched intermediates. It has been employed in research toward central nervous system agents and enzyme inhibitors. Its h

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports the formation of nitrogen-containing heterocycles, which are common in medicinal chemistry. The compound is valuable in asymmetric synthesis due to its stereochemical purity, enabling the production of enantiomerically enriched intermediates. It has been employed in research toward central nervous system agents and enzyme inhibitors. Its hydrochloride salt form enhances stability and solubility, facilitating handling in synthetic routes.

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