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(2S)-N~1~,N~1~-diethyl-3-(1H-indol-3-yl)propane-1,2-diamine is a chiral diamine compound characterized by its specific three-dimensional arrangement of atoms, indicated by the (2S) configuration. It features two amino groups and an indole ring, a bicyclic heterocyclic structure prevalent in natural products and pharmaceuticals. (2S)-N~1~,N~1~-diethyl-3-(1H-indol-3-yl)propane-1,2-diamine's structure suggests its potential use in medicinal chemistry, particularly for the development of drugs that target specific biological pathways or receptors. Its chiral nature is also significant for its biological activity and potential therapeutic effects.

53708-57-9

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53708-57-9 Usage

Uses

Used in Medicinal Chemistry:
(2S)-N~1~,N~1~-diethyl-3-(1H-indol-3-yl)propane-1,2-diamine is used as a building block or intermediate in the synthesis of pharmaceuticals for its potential to target specific biological pathways or receptors. Its unique structure and chirality may contribute to the development of new drugs with enhanced efficacy and selectivity.
Used in Drug Development:
In the pharmaceutical industry, (2S)-N~1~,N~1~-diethyl-3-(1H-indol-3-yl)propane-1,2-diamine is utilized as a key component in the design and development of innovative drugs. Its presence in natural products and its compatibility with biological systems make it a promising candidate for creating therapeutic agents with improved pharmacological properties.
Used in Chiral Compound Research:
(2S)-N~1~,N~1~-diethyl-3-(1H-indol-3-yl)propane-1,2-diamine is employed in research settings to study the effects of chirality on biological activity. Understanding how the (2S) configuration influences the compound's interaction with biological targets can lead to the discovery of more effective and safer medications.
Used in Natural Product Synthesis:
Given its presence in natural products, (2S)-N~1~,N~1~-diethyl-3-(1H-indol-3-yl)propane-1,2-diamine is used in the synthesis of complex natural compounds. Its structural features facilitate the creation of novel bioactive molecules with potential applications in various therapeutic areas.

Check Digit Verification of cas no

The CAS Registry Mumber 53708-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,0 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53708-57:
(7*5)+(6*3)+(5*7)+(4*0)+(3*8)+(2*5)+(1*7)=129
129 % 10 = 9
So 53708-57-9 is a valid CAS Registry Number.

53708-57-9Relevant academic research and scientific papers

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