(S)-3-Amino-piperidine-2,6-dione hydrochloride

98%

Reagent Code: #236008
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CAS Number 25181-50-4

science Other reagents with same CAS 25181-50-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.59 g/mol
Formula C₅H₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD15474943
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in the synthesis of pharmaceutical agents, particularly as an intermediate in the production of immunomodulatory drugs. It plays a key role in the development of compounds that target cytokine modulation and angiogenesis inhibition. Commonly utilized in the preparation of analogs related to thalidomide and lenalidomide, it contributes to treatments for hematological cancers such as multiple myeloma and myelodysplastic syndromes. Its chiral structure makes it valuable for creating enantiomerically pure drugs with improved efficacy and reduced side effects. Also employed in research settings for exploring new therapeutic agents in oncology and inflammatory diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿400.00
inventory 250mg
10-20 days ฿530.00
inventory 1g
10-20 days ฿710.00
inventory 25g
10-20 days ฿7,510.00
inventory 100g
10-20 days ฿26,090.00
inventory 5g
10-20 days ฿2,220.00

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(S)-3-Amino-piperidine-2,6-dione hydrochloride
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Used primarily in the synthesis of pharmaceutical agents, particularly as an intermediate in the production of immunomodulatory drugs. It plays a key role in the development of compounds that target cytokine modulation and angiogenesis inhibition. Commonly utilized in the preparation of analogs related to thalidomide and lenalidomide, it contributes to treatments for hematological cancers such as multiple myeloma and myelodysplastic syndromes. Its chiral structure makes it valuable for creating enantiome

Used primarily in the synthesis of pharmaceutical agents, particularly as an intermediate in the production of immunomodulatory drugs. It plays a key role in the development of compounds that target cytokine modulation and angiogenesis inhibition. Commonly utilized in the preparation of analogs related to thalidomide and lenalidomide, it contributes to treatments for hematological cancers such as multiple myeloma and myelodysplastic syndromes. Its chiral structure makes it valuable for creating enantiomerically pure drugs with improved efficacy and reduced side effects. Also employed in research settings for exploring new therapeutic agents in oncology and inflammatory diseases.

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