2-(2-Chloroethyl)-N-methyl-pyrrolidine hydrochloride

  • CAS:56824-22-7
  • MF:C7H14ClN.HCl
  • Purity:99%
  • Molecular Weight:184.109
Get the best price

Product Details

  • CAS: 56824-22-7
  • MF: C7H14ClN.HCl
  • Appearance: light liquids
  • Factory Sells Best Quality 2-(2-Chloroethyl)-N-methyl-pyrrolidine hydrochloride 56824-22-7 with ISO standards

    • Molecular Formula:C7H14ClN*ClH
    • Molecular Weight:184.109
    • Appearance/Colour:light liquids 
    • Melting Point:98-102 °C 
    • Boiling Point:181.5 °C at 760 mmHg 
    • Flash Point:63.6 °C 
    • PSA:3.24000 
    • LogP:2.44940 

    2-(2-Chloroethyl)-N-methyl-pyrrolidine hydrochloride(Cas 56824-22-7) Usage

    InChI:InChI=1/C7H14ClN.ClH/c1-9-6-2-3-7(9)4-5-8;/h7H,2-6H2,1H3;1H

    56824-22-7 Relevant articles

    Design, synthesis, and biological evaluation of 3,4-dihydroquinolin-2(1 H)-one and 1,2,3,4-tetrahydroquinoline-based selective human neuronal nitric oxide synthase (nNOS) inhibitors

    Ramnauth, Jailall,Speed, Joanne,Maddaford, Shawn P.,Dove, Peter,Annedi, Subhash C.,Renton, Paul,Rakhit, Suman,Andrews, John,Silverman, Sarah,Mladenova, Gabriela,Zinghini, Salvatore,Nair, Sheela,Catalano, Concettina,Lee, David K.H.,De Felice, Milena,Porreca, Frank

    , p. 5562 - 5575 (2011)

    Neuronal nitric oxide synthase (nNOS) in...

    Preparation method of clomastine fumarate with high chiral purity

    -

    Paragraph 0016; 0021, (2020/07/15)

    The invention discloses a preparation me...

    Asymmetric synthesis of H1 receptor antagonist (R,R)-clemastine

    Lee, Sun Young,Jung, Jung Wha,Kim, Tae-Hyun,Kim, Hee-Doo

    , p. 2131 - 2136 (2015/12/08)

    The first asymmetric synthesis of (R,R)-...

    Synthesis of (-)-(S, S)-clemastine by invertive N → C aryl migration in a lithiated carbamate

    Fournier, Anne M.,Brown, Robert A.,Farnaby, William,Miyatake-Ondozabal, Hideki,Clayden, Jonathan

    supporting information; experimental part, p. 2222 - 2225 (2010/08/04)

    The first enantioselective synthesis of ...

    56824-22-7 Process route

    R(+)-1-methyl-2-(2-hydroxyethyl)pyrrolidine
    60307-26-8

    R(+)-1-methyl-2-(2-hydroxyethyl)pyrrolidine

    (+)-(R)-2-(2-chloroethyl)-1-methylpyrrolidine hydrochloride
    67499-71-2,56824-22-7

    (+)-(R)-2-(2-chloroethyl)-1-methylpyrrolidine hydrochloride

    Conditions
    Conditions Yield
    With thionyl chloride; In chloroform; at 0 ℃; for 1h; Reflux;
    100%
    R(+)-1-methyl-2-(2-hydroxyethyl)pyrrolidine; With hydrogenchloride; In chloroform; for 0.5h;
    With thionyl chloride; In chloroform; for 2h; Reflux;
    77%
    With thionyl chloride; In chloroform; at 0 ℃; Reflux;
    With thionyl chloride; In dichloromethane; at 0 - 25 ℃; for 2h;
    (-)-2-((S)-1-methylpyrrolidin-2-yl)ethanol
    61810-78-4

    (-)-2-((S)-1-methylpyrrolidin-2-yl)ethanol

    (-)-(S)-2-(2-chloroethyl)-1-methylpyrrolidine hydrochloride
    67529-18-4,56824-22-7

    (-)-(S)-2-(2-chloroethyl)-1-methylpyrrolidine hydrochloride

    Conditions
    Conditions Yield
    With thionyl chloride; In chloroform; at 0 ℃; Reflux;
    92%

    56824-22-7 Upstream products

    • 60307-26-8
      60307-26-8

      R(+)-1-methyl-2-(2-hydroxyethyl)pyrrolidine

    • 1352748-96-9
      1352748-96-9

      (S)-ethyl 2-(2-hydroxyethyl)-2,5-dihydro-1H-pyrrole-1-carboxylate

    • 67004-64-2
      67004-64-2

      2-(1-methyl-2-pyrrolidine)ethanol

    • 61810-78-4
      61810-78-4

      (-)-2-((S)-1-methylpyrrolidin-2-yl)ethanol

    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

    Contact Now

    We will contact you as soon as possible


    提交