(S)-Methyl 6-(1-aminoethyl)nicotinate hydrochloride

95%

Reagent Code: #233207
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CAS Number 1236349-85-1

science Other reagents with same CAS 1236349-85-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.66 g/mol
Formula C₉H₁₃ClN₂O₂
badge Registry Numbers
MDL Number MFCD28405344
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used in the synthesis of varenicline, a medication for smoking cessation. It serves as a key chiral intermediate in pharmaceutical manufacturing, enabling the production of the active ingredient with high enantiomeric purity. The compound's structure allows for selective chemical transformations critical to forming varenicline’s bicyclic framework. Its hydrochloride salt form improves stability and handling during synthesis. Widely utilized in multi-step routes to ensure yield efficiency and stereochemical control.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,490.00
inventory 250mg
10-20 days ฿22,020.00

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(S)-Methyl 6-(1-aminoethyl)nicotinate hydrochloride
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Used in the synthesis of varenicline, a medication for smoking cessation. It serves as a key chiral intermediate in pharmaceutical manufacturing, enabling the production of the active ingredient with high enantiomeric purity. The compound's structure allows for selective chemical transformations critical to forming varenicline’s bicyclic framework. Its hydrochloride salt form improves stability and handling during synthesis. Widely utilized in multi-step routes to ensure yield efficiency and stereochemic

Used in the synthesis of varenicline, a medication for smoking cessation. It serves as a key chiral intermediate in pharmaceutical manufacturing, enabling the production of the active ingredient with high enantiomeric purity. The compound's structure allows for selective chemical transformations critical to forming varenicline’s bicyclic framework. Its hydrochloride salt form improves stability and handling during synthesis. Widely utilized in multi-step routes to ensure yield efficiency and stereochemical control.

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