Cas no 1213035-71-2 ((S)-1-(2-Chloro-pyridin-4-YL)-propylamine)

(S)-1-(2-Chloro-pyridin-4-YL)-propylamine is a chiral amine derivative featuring a 2-chloropyridyl substituent, offering utility as a versatile intermediate in pharmaceutical and agrochemical synthesis. Its stereospecific (S)-configuration ensures high enantiopurity, making it valuable for asymmetric synthesis and chiral catalyst development. The presence of the chloro-pyridinyl group enhances reactivity in cross-coupling reactions, while the propylamine backbone provides flexibility for further functionalization. This compound is particularly useful in the preparation of biologically active molecules, including ligands and active pharmaceutical ingredients (APIs). Its stability under standard storage conditions and compatibility with common organic solvents further underscore its practicality in industrial and research applications.
(S)-1-(2-Chloro-pyridin-4-YL)-propylamine structure
1213035-71-2 structure
Product Name:(S)-1-(2-Chloro-pyridin-4-YL)-propylamine
CAS No:1213035-71-2
MF:C8H11ClN2
MW:170.639340639114
MDL:MFCD09256921
CID:4773565
Update Time:2026-02-26

(S)-1-(2-Chloro-pyridin-4-YL)-propylamine Chemical and Physical Properties

Names and Identifiers

    • (S)-1-(2-CHLORO-PYRIDIN-4-YL)-PROPYLAMINE
    • SB31803
    • (S)-1-(2-Chloropyridin-4-yl)propan-1-amine
    • (1S)-1-(2-chloropyridin-4-yl)propan-1-amine
    • (S)-1-(2-Chloro-pyridin-4-YL)-propylamine
    • MDL： MFCD09256921
    • Inchi： 1S/C8H11ClN2/c1-2-7(10)6-3-4-11-8(9)5-6/h3-5,7H,2,10H2,1H3/t7-/m0/s1
    • InChI Key： NAEAXIYCMLCDSF-ZETCQYMHSA-N
    • SMILES： ClC1C=C(C=CN=1)[C@H](CC)N

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 119
  • XLogP3: 1.6
  • Topological Polar Surface Area: 38.9

(S)-1-(2-Chloro-pyridin-4-YL)-propylamine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd.
69R0703-5g
(S)-1-(2-Chloro-pyridin-4-yl)-propylamine
 1213035-71-2 96%
5g
 40960.45CNY 2021-05-07
JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd.
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 1213035-71-2 96%
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eNovation Chemicals LLC
Y1293101-1g
(S)-1-(2-Chloro-pyridin-4-yl)-propylamine
 1213035-71-2 95%
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eNovation Chemicals LLC
Y1293101-5g
(S)-1-(2-Chloro-pyridin-4-yl)-propylamine
 1213035-71-2 95%
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 $5550 2023-05-18
JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd.
69R0703-5g
(S)-1-(2-Chloro-pyridin-4-yl)-propylamine
 1213035-71-2 96%
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JIE DA WEI （ SHANG HAI ） YI YAO KE JI FA ZHAN Co., Ltd.
69R0703-1g
(S)-1-(2-Chloro-pyridin-4-yl)-propylamine
 1213035-71-2 96%
1g
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SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1944964-1g
(s)-1-(2-Chloropyridin-4-yl)propan-1-amine
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(S)-1-(2-Chloro-pyridin-4-YL)-propylamine Related Literature

Additional information on (S)-1-(2-Chloro-pyridin-4-YL)-propylamine

Comprehensive Overview of (S)-1-(2-Chloro-pyridin-4-YL)-propylamine (CAS No. 1213035-71-2)

(S)-1-(2-Chloro-pyridin-4-YL)-propylamine (CAS No. 1213035-71-2) is a chiral amine derivative with significant applications in pharmaceutical research and organic synthesis. This compound, characterized by its 2-chloropyridine moiety and propylamine chain, has garnered attention due to its potential as a building block for bioactive molecules. Its stereospecificity and structural versatility make it a valuable intermediate in the development of enantioselective catalysts and therapeutic agents.

In recent years, the demand for chiral amines like (S)-1-(2-Chloro-pyridin-4-YL)-propylamine has surged, driven by advancements in asymmetric synthesis and drug discovery. Researchers are particularly interested in its role in designing kinase inhibitors and neuroactive compounds, aligning with trends in personalized medicine. The compound's CAS No. 1213035-71-2 is frequently searched in academic databases, reflecting its relevance in medicinal chemistry and process optimization.

The synthesis of (S)-1-(2-Chloro-pyridin-4-YL)-propylamine typically involves enantioselective reduction or resolution techniques, with yields optimized through green chemistry principles. Its pyridine core offers stability and reactivity, enabling derivatization for diverse applications. Analytical methods such as HPLC and chiral chromatography are essential for verifying its enantiomeric purity, a critical parameter for regulatory compliance.

From an industrial perspective, scalability and cost-efficiency are key considerations for CAS No. 1213035-71-2. Innovations in continuous flow chemistry and biocatalysis have been explored to address these challenges. Environmental sustainability is another hotspot, with studies focusing on solvent-free reactions and catalytic recycling to minimize waste.

In summary, (S)-1-(2-Chloro-pyridin-4-YL)-propylamine exemplifies the intersection of chiral technology and drug development. Its CAS No. 1213035-71-2 serves as a gateway for researchers exploring novel synthetic routes and therapeutic candidates, ensuring its enduring relevance in scientific literature and industrial applications.

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