(S)-4-(Pyrrolidin-3-yl)thiomorpholine dihydrochloride

95%

Reagent Code: #233508
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CAS Number 1821826-02-1

science Other reagents with same CAS 1821826-02-1

blur_circular Chemical Specifications

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Weight 245.21 g/mol
Formula C₈H₁₈Cl₂N₂S
badge Registry Numbers
MDL Number MFCD28023892
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used in pharmaceutical research as a chiral building block for synthesizing biologically active compounds. Its structure supports the development of enzyme inhibitors and receptor modulators, particularly in neuroscience and metabolic disease therapies. The compound's stereochemistry makes it valuable in creating selective drug candidates. It is also employed in the synthesis of novel thiomorpholine-based derivatives with potential antimicrobial and anticancer properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid, functionalized ring system.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,250.00
inventory 250mg
10-20 days ฿8,920.00
inventory 1g
10-20 days ฿24,070.00

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(S)-4-(Pyrrolidin-3-yl)thiomorpholine dihydrochloride
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Used in pharmaceutical research as a chiral building block for synthesizing biologically active compounds. Its structure supports the development of enzyme inhibitors and receptor modulators, particularly in neuroscience and metabolic disease therapies. The compound's stereochemistry makes it valuable in creating selective drug candidates. It is also employed in the synthesis of novel thiomorpholine-based derivatives with potential antimicrobial and anticancer properties. Commonly utilized in medicinal c

Used in pharmaceutical research as a chiral building block for synthesizing biologically active compounds. Its structure supports the development of enzyme inhibitors and receptor modulators, particularly in neuroscience and metabolic disease therapies. The compound's stereochemistry makes it valuable in creating selective drug candidates. It is also employed in the synthesis of novel thiomorpholine-based derivatives with potential antimicrobial and anticancer properties. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid, functionalized ring system.

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