1501-84-4

  • Product Name:Rimantadine hydrochloride
  • Molecular Formula:C12H22ClN
  • Purity:99%
  • Molecular Weight:215.766
Inquiry

Product Details;

CasNo: 1501-84-4

Molecular Formula: C12H22ClN

Appearance: white crystalline solid

Buy Quality Trustworthy Manufacturer Supply Rimantadine hydrochloride 1501-84-4 with Safe Delivery

  • Molecular Formula:C12H21N*ClH
  • Molecular Weight:215.766
  • Appearance/Colour:white crystalline solid 
  • Vapor Pressure:0.0251mmHg at 25°C 
  • Melting Point:>300 °C 
  • Boiling Point:247.8 °C at 760 mmHg 
  • Flash Point:99.3 °C 
  • PSA:26.02000 
  • LogP:4.05230 

Rimantadine hydrochloride(Cas 1501-84-4) Usage

Description

Rimantadine hydrochloride is an antiviral analogue of amantadine, reportedly useful in the prophylaxis and treatment of influenza A. Compared with amantadine, nmantadine appears to have a lower side-effect profile.

Chemical Properties

White Crystalline Solid

Originator

DuPont (USA)

Uses

Rimantadine Hydrochloride is used as an antiviral agent.

Brand name

Flumadine (Forest);Roflual.

references

[1] koff w c, elm jr j l, halstead s b. suppression of dengue virus replication in vitro by rimantadine hydrochloride[j]. the american journal of tropical medicine and hygiene, 1981, 30(1): 184-189.[2] koff w c, peavy d l, knight v. inhibition of in vitro proliferative responses of human lymphocytes by rimantadine hydrochloride[j]. infection and immunity, 1979, 23(3): 665-669.[3] hayden f g, monto a s. oral rimantadine hydrochloride therapy of influenza a virus h3n2 subtype infection in adults[j]. antimicrobial agents and chemotherapy, 1986, 29(2): 339-341.

InChI:InChI=1/C12H21N.ClH/c1-8(13)12-5-9-2-10(6-12)4-11(3-9)7-12;/h8-11H,2-7,13H2,1H3;1H

1501-84-4 Relevant articles

Preparation method of rimantadine hydrochloride preparation

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Paragraph 0026; 0033; 0042; 0051, (2019/02/04)

The invention discloses a preparation me...

Synthesizing method of rimantadine hydrochloride

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Paragraph 0022; 0025; 0032; 0040; 0048, (2019/02/21)

The invention discloses a synthesizing m...

A kind of anti-influenza virus preparation

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Paragraph 0026; 0033; 0042; 0051, (2019/03/15)

The present invention discloses an anti-...

Process for preparing rimantadine

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, (2008/06/13)

A low temperature and pressure process f...

1501-84-4 Process route

1-((3r,5r,7r)-adamantan-1-yl)ethan-1-one oxime
1707-40-0

1-((3r,5r,7r)-adamantan-1-yl)ethan-1-one oxime

rimantadine hydrochloride
1501-84-4,33122-80-4,33122-81-5,33298-76-9

rimantadine hydrochloride

Conditions
Conditions Yield
1-((3r,5r,7r)-adamantan-1-yl)ethan-1-one oxime; With palladium on activated charcoal; hydrogen; acetic acid; at 20 ℃; for 18h; under 3000.3 Torr; Autoclave;
With hydrogenchloride; In water; Pressure;
95%
1-((3r,5r,7r)-adamantan-1-yl)ethan-1-one oxime; With L-Tartaric acid; palladium on activated charcoal; hydrogen; acetic acid; at 20 ℃; for 18h; under 3000.3 Torr; Autoclave; Green chemistry;
With hydrogenchloride; Pressure; Reagent/catalyst; Green chemistry;
95%
1-((3r,5r,7r)-adamantan-1-yl)ethan-1-one oxime; With metatartaric acid; palladium on activated charcoal; hydrogen; acetic acid; at 20 ℃; for 18h; under 3000.3 Torr; Autoclave;
With hydrogenchloride; Pressure;
95%
1-adamantyl methyl ketoxime
78679-71-7

1-adamantyl methyl ketoxime

rimantadine hydrochloride
1501-84-4,33122-80-4,33122-81-5,33298-76-9

rimantadine hydrochloride

Conditions
Conditions Yield
With hydrogenchloride; hydrogen; Pt/C; In dichloromethane; water; acetic acid; ethyl acetate;
75%
With hydrogenchloride; Pt/C; In ethanol; water;

1501-84-4 Upstream products

  • 78679-71-7
    78679-71-7

    1-adamantyl methyl ketoxime

  • 1707-40-0
    1707-40-0

    1-((3r,5r,7r)-adamantan-1-yl)ethan-1-one oxime

  • 281-23-2
    281-23-2

    adamantane

  • 768-90-1
    768-90-1

    1-Adamantyl bromide

1501-84-4 Downstream products

  • 90812-24-1
    90812-24-1

    3-(1-aminoethyl)adamantan-1-ol hydrochloride

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