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Ozanimod hydrochloride

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Company Name: Shijiazhuang Dingmin Pharmaceutical Sciences Co., Ltd.
Tel: +86-0311-67591193 +8613931880626
Email: sales02@dingminpharma.com
Products Intro: Product Name:Ozanimod Hcl
CAS:1618636-37-5
Purity:99.5%+ Package:100g;1kg;10kg
Company Name: Hebei Dangtong Import and export Co LTD
Tel: +86-86-4001020630 +8619831957301
Email: admin@hbdangtong.com
Products Intro: Product Name:Ozanimod hydrochloride
CAS:1618636-37-5
Purity:99% Package:1kg;16500USD|5kg;15000USD|10kg;14000USD
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Products Intro: Product Name:Ozanimod hydrochloride
CAS:1618636-37-5
Purity:99.81% Package:1mg;61USD|5mg;142USD|10mg;213USD
Company Name: Guangzhou TongYi biochemistry technology Co.,LTD
Tel: +8613073028829
Email: tongyibiochem@163.com
Products Intro: Product Name:Ozanimod Hydrochloride
CAS:1618636-37-5
Purity:99% Package:1g,10g,100g,500g,1kg,25kg,100kg,500kg
Company Name: Senova Technology Co. Ltd.
Tel: +86-0755-86703119 +8618503098836
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Products Intro: Product Name:(S)-4-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-N-(2-hydroxyethyl)-2,3-dihydro-1H-inden-1-aminium chloride
CAS:1618636-37-5
Purity:0.99 Package:25kg

Ozanimod hydrochloride manufacturers

  • Ozanimod hydrochloride
  • Ozanimod hydrochloride pictures
  • $16500.00 / 1kg
  • 2026-02-25
  • CAS:1618636-37-5
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 100KG

Related articles

  • Synthesis of Ozanimod Hydrochloride
  • Ozanimod Hydrochloride is prepared from the eastern fragment joined to the western fragment to form a central oxadiazole ring ....
  • Dec 28,2023
Ozanimod hydrochloride Basic information
Product Name:Ozanimod hydrochloride
Synonyms:Ozanimod hydrochloride;Ozanimod hydrochloride Impurity 1;(S)-4-(5-(3-cyano-4-isopropoxyphenyl)-1,2,4-oxadiazol-3-yl)-N-(2-hydroxyethyl)-2,3-dihydro-1H-inden-1-aminium chloride;Ozanimod hyd;(S)-5-(3-(1-((2-Hydroxyethyl)amino)-2,3-dihydro-1H-inden-4-yl)-1,2,4-oxadiazol-5-yl)-2-isopropoxybenzonitrile hydrochloride;"Benzonitrile, 5-[3-[(1S)-2,3-dihydro-1- [(2-hydroxyethyl)amino]-1H-inden-4-yl]-1,2,4-oxadiazol-5-yl]-2-(1-methyleth";5-[3-[(1S)-1-(2-hydroxyethylamino)-2,3-dihydro-1H-inden-4-yl]-1,2,4-oxadiazol-5-yl]-2-propan-2-yloxybenzonitrile;Ozanimod hydrochloride,1618636-37-5,Pharmaceutical Chemicals
CAS:1618636-37-5
MF:C23H25ClN4O3
MW:440.93
EINECS:
Product Categories:
Mol File:1618636-37-5.mol
Ozanimod hydrochloride Structure
Ozanimod hydrochloride Chemical Properties
form Solid
color White to off-white
InChIKeyHAOOCAKHSFYDBU-OZYVVJTJNA-N
SMILESN([C@H]1CCC2=C(C3=NOC(C4C=CC(OC(C)C)=C(C#N)C=4)=N3)C=CC=C12)CCO.Cl |&1:1,r|
Safety Information
MSDS Information
Ozanimod hydrochloride Usage And Synthesis
DescriptionOzanimod hydrochloride (RPC-1063 hydrochloride) is an orally available, selective and potent sphingosine 1-phosphate (S1P) receptor modulator that shows high affinity for S1P1 and S1P5. Ozanimod has potential anticancer activity and can be used in studying multiple sclerosis (MS), ulcerative multiple sclerosis (UMS), and other diseases. (MS), ulcerative colitis, coronavirus infections and myelodysplasia.
Chemical Properties Ozanimod hydrochloride is a white to off-white solid with a melting point of ~240°C. It is poorly hygroscopic. The solubility of ozanimod hydrochloride in ethanol and methanol is 1.43 and 2.41 mg/mL; in a pH 5.1, aqueous medium is 3.51 mg/mL. The pKa for this compound is 7.90, and the partition coefficient (logP) is 3.28.
UsesOzanimod hydrochloride is an oral sphingosine 1-phosphate receptor modulator used to treat ulcerative colitis and other autoimmune diseases.
Synthesis The carboxylic acid 187 (Western fragment) was activated using CDI (carbodiimide) and then coupled with the Eastern fragment 186 to form the oxadiazole 189. The crude product was used directly for the subsequent acetal deprotection without further purification. The deprotection reaction gave the ketone 190 in 76% yield from 187. The ketone 190 was condensed with 2-aminoethyl alcohol under Dean-Stark conditions to give the imine 191 in 96% yield. The chiral ruthenium complex 192 catalyzed the reduction of the imine 190 to give ozanimod 193 in high enantiomeric excess. Finally, the salt formation reaction with hydrochloric acid in methanol gave ozanimod hydrochloride in high yield.
Ozanimod hydrochloride synthesis
Ozanimod hydrochloride Preparation Products And Raw materials
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