Cas no 5949-16-6 (Cinchonine Hemisulfate Salt)

Cinchonine Hemisulfate Salt is a quinine alkaloid derivative, commonly utilized in chiral resolution and asymmetric synthesis due to its stereoselective properties. The hemisulfate form enhances solubility in aqueous and polar organic solvents, facilitating its use in catalytic and analytical applications. It serves as a versatile chiral auxiliary or ligand in enantioselective reactions, particularly in the pharmaceutical and fine chemical industries. The compound’s rigid bicyclic structure contributes to its high selectivity in binding and separating enantiomers. Its stability under standard conditions and well-characterized reactivity make it a reliable reagent for research and industrial processes requiring precise stereochemical control.
Cinchonine Hemisulfate Salt structure
Cinchonine Hemisulfate Salt structure
Product Name:Cinchonine Hemisulfate Salt
CAS No:5949-16-6
MF:C38H46N4O6S
MW:686.8600
MDL:MFCD00035639
CID:369002
PubChem ID:87565860
Update Time:2025-05-23

Cinchonine Hemisulfate Salt Chemical and Physical Properties

Names and Identifiers

    • Cinchonine sulphate
    • Cinchonine Sulfate Dihydrate
    • cinchonine hemisulfate
    • CINCHONINE HEMISULFATE CRYSTALLINE
    • Cinchonine hemisulfate salt
    • CINCHONINE SULFATE
    • CinchonineSulfateDihydrate
    • CINCHONINE SULFATE [WHO-DD]
    • (S)-Quinolin-4-yl((1S,2R,4S,5R)-5-vinylquinuclidin-2-yl)methanol hemisulfate
    • GNF-Pf-3189
    • Cinchonine sulfate, anhydrous
    • D-CINCHONINE, SULPHATE (2:1) (SALT)
    • BS-44076
    • Cinchonine sulfate [NF]
    • (S)-[(2R,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-quinolin-4-ylmethanol;sulfuric acid
    • Cinchonine hemisulfate salt, analytical standard
    • D-CINCHONINE, SULFATE (2:1) (SALT)
    • EINECS 227-708-4
    • Q27256319
    • 2-QUINUCLIDINEMETHANOL, ALPHA-(5-VINYL-2-QUINOLYL)-, SULFATE (2:1) (SALT)
    • Cinchonan-9-ol, (9S)-, sulfate (2:1) (salt)
    • CINCHONINE, SULPHATE (2:1) (SALT)
    • CHEMBL2105783
    • CINCHONINE, SULFATE (2:1) (salt)
    • UNII-342JR840KF
    • Anhydrous cinchonine sulfate
    • CINCHONAN-9-OL, (9S)-, SULPHATE (2:1) (SALT)
    • 2-QUINUCLIDINEMETHANOL, ALPHA-(5-VINYL-2-QUINOLYL)-, SULPHATE (2:1) (SALT)
    • CINCHONINUM SULPHURICUM [HPUS]
    • 2-QUINUCLIDINEMETHANOL, .ALPHA.-(5-VINYL-2-QUINOLYL)-, SULPHATE (2:1) (SALT)
    • 342JR840KF
    • (+)-CINCONINE SULFATE
    • (+)-CINCONINE SULPHATE
    • Cinchoninum sulphuricum
    • (8R,9S)-CINCHONINE, SULPHATE (2:1) (SALT)
    • WBBHOISPYYYBTC-SJFRDBBCSA-N
    • 2-QUINUCLIDINEMETHANOL, .ALPHA.-(5-VINYL-2-QUINOLYL)-, SULFATE (2:1) (SALT)
    • Cinchonine sulfate anhydrous
    • (8R,9S)-CINCHONINE, SULFATE (2:1) (SALT)
    • 5949-16-6
    • TCMDC-123933
    • Cinchonine Hemisulfate Salt
    • MDL: MFCD00035639
    • Inchi: 1S/2C19H22N2O.H2O4S/c2*1-2-13-12-21-10-8-14(13)11-18(21)19(22)16-7-9-20-17-6-4-3-5-15(16)17;1-5(2,3)4/h2*2-7,9,13-14,18-19,22H,1,8,10-12H2;(H2,1,2,3,4)/t2*13-,14+,18-,19-;/m00./s1
    • InChI Key: WBBHOISPYYYBTC-VVECRAFTSA-N
    • SMILES: S(=O)(=O)(O[H])O[H].O([H])[C@@]([H])(C1=C([H])C([H])=NC2=C([H])C([H])=C([H])C([H])=C12)[C@]1([H])C([H])([H])[C@@]2([H])C([H])([H])C([H])([H])N1C([H])([H])[C@]2([H])C([H])=C([H])[H].O([H])[C@@]([H])(C1=C([H])C([H])=NC2=C([H])C([H])=C([H])C([H])=C12)[C@]1([H])C([H])([H])[C@@]2([H])C([H])([H])C([H])([H])N1C([H])([H])[C@]2([H])C([H])=C([H])[H]

Computed Properties

  • Exact Mass: 686.31400
  • Monoisotopic Mass: 392.14059304g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 10
  • Heavy Atom Count: 49
  • Rotatable Bond Count: 6
  • Complexity: 494
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 8
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Topological Polar Surface Area: 156

Experimental Properties

  • Color/Form: Not determined
  • Melting Point: 206 C
  • PSA: 155.70000
  • LogP: 6.63300
  • Sensitiveness: Sensitive to light
  • Solubility: Not determined

Cinchonine Hemisulfate Salt Security Information

  • Symbol: GHS07
  • Prompt:warning
  • Hazard Statement: H302
  • Warning Statement: P264-P270-P301+P312+P330-P501
  • Hazardous Material transportation number:1544
  • WGK Germany:3
  • Hazard Category Code: 36/37/38
  • Safety Instruction: S26; S36
  • Regulatory Condition Code:Class Q (sugars, alkaloids, antibiotics, hormones)
  • RTECS:GD3800000
  • Hazardous Material Identification: Xi
  • HazardClass:6.1(b)
  • PackingGroup:III
  • Risk Phrases:R36/37/38
  • Packing Group:III
  • Safety Term:6.1(b)
  • Packing Group:III
  • Hazard Level:6.1(b)

Cinchonine Hemisulfate Salt Pricemore >>

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Cinchonine Hemisulfate Salt Suppliers

Amadis Chemical Company Limited
Gold Member
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(CAS:5949-16-6)Cinchonine Hemisulfate Salt
Order Number:A914312
Stock Status:in Stock
Quantity:100g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 12:51
Price ($):165.0
Tiancheng Chemical (Jiangsu) Co., Ltd
Gold Member
Audited Supplier Audited Supplier
(CAS:5949-16-6)Cinchonine Sulfate Dihydrate, ≥ 98.0%
Order Number:LE17337
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:16
Price ($):discuss personally

Additional information on Cinchonine Hemisulfate Salt

Cinchonine Hemisulfate Salt (CAS No. 5949-16-6): A Comprehensive Overview

Cinchonine Hemisulfate Salt, also known by its CAS registry number 5949-16-6, is a compound of significant interest in the fields of pharmacology, natural product chemistry, and drug discovery. This compound, a hemisulfate salt of cinchonine, has garnered attention due to its unique chemical properties and potential therapeutic applications. Recent advancements in research have shed light on its mechanisms of action, bioavailability, and potential uses in treating various diseases.

Cinchonine, the parent compound of Cinchonine Hemisulfate Salt, is a naturally occurring alkaloid found in certain species of Cinchona trees. These trees have been historically valued for their medicinal properties, particularly in the treatment of malaria. The isolation and characterization of cinchonine have opened new avenues for its use in modern medicine. The hemisulfate salt form enhances its solubility and stability, making it more amenable for pharmaceutical applications.

Recent studies have explored the antitumor activity of Cinchonine Hemisulfate Salt, revealing its potential as a chemotherapeutic agent. Researchers have demonstrated that this compound can induce apoptosis in various cancer cell lines, suggesting its role in targeting proliferative diseases. Additionally, its ability to modulate cellular signaling pathways has been extensively investigated, providing insights into its mechanism of action.

The chemical structure of Cinchonine Hemisulfate Salt comprises a quinoline skeleton with hydroxyl and methoxy groups, contributing to its unique pharmacokinetic properties. These functional groups not only influence its bioavailability but also play a crucial role in its interactions with cellular targets. Advanced computational methods, such as molecular docking studies, have been employed to elucidate the binding affinities of this compound with key proteins involved in disease pathways.

In terms of therapeutic applications, Cinchonine Hemisulfate Salt has shown promise in the treatment of infectious diseases. Its antimicrobial properties have been tested against a range of pathogens, including bacteria and fungi. Furthermore, preclinical studies have highlighted its potential as an immunomodulatory agent, capable of regulating immune responses in inflammatory conditions.

The synthesis and purification of Cinchonine Hemisulfate Salt have also been optimized using green chemistry principles. This approach not only enhances the efficiency of production but also reduces environmental impact, aligning with current trends toward sustainable drug manufacturing.

From a pharmacological standpoint, the bioavailability and pharmacokinetics of Cinchonine Hemisulfate Salt have been thoroughly examined. Studies indicate that this compound exhibits favorable absorption profiles when administered orally or via other routes, making it suitable for systemic delivery.

In conclusion, Cinchonine Hemisulfate Salt (CAS No. 5949-16-6) represents a valuable addition to the arsenal of natural product-derived compounds with diverse therapeutic potentials. Ongoing research continues to uncover new insights into its mechanisms and applications, underscoring its importance in contemporary drug discovery efforts.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:5949-16-6)Cinchonine Hemisulfate Salt
A914312
Purity:99%
Quantity:100g
Price ($):165.0
Email
Tiancheng Chemical (Jiangsu) Co., Ltd
(CAS:5949-16-6)Cinchonine Sulfate Dihydrate, ≥ 98.0%
LE17337
Purity:99%
Quantity:25KG,200KG,1000KG
Price ($):Inquiry
Email