免费v片在线观看视频网站软件亮点,亚洲最大AV资源网在线观看,亚洲精品ⅴ在线观看,2021真实偷拍各种走光福利

  • <sup id="33bym"></sup>
    1. <strike id="33bym"></strike>
      <ol id="33bym"></ol>
    2. Organic Intermediates: Pharmaceutical Intermediates

      Home - Products List - Organic Intermediates: Pharmaceutical Intermediates

      Cyclen

      • Product Name: Cyclen
      • CAS: 294-90-6
      • Purity:
      • Appearance: off- white to slightly yellow crystalline powder

      Contact Us: +86-15508631887(WhatsApp/WeChat)

      Email:sales@finerchem.com

      Inquiry

      Factory Supply industrial standard Cyclen 294-90-6 In Stock

      • Molecular Formula:C8H20N4
      • Molecular Weight:172.274
      • Appearance/Colour:off- white to slightly yellow crystalline powder 
      • Vapor Pressure:0.00309mmHg at 25°C 
      • Melting Point:108-113 °C 
      • Refractive Index:1.5872 (estimate) 
      • Boiling Point:283.8 °C at 760 mmHg 
      • PKA:10.53±0.20(Predicted) 
      • Flash Point:129.5 °C 
      • PSA:48.12000 
      • Density:0.874 g/cm3 
      • LogP:-0.32640 

      Cyclen(Cas 294-90-6) Usage

      Synthesis Reference(s)

      Journal of the American Chemical Society, 96, p. 2268, 1974 DOI: 10.1021/ja00814a056

      Flammability and Explosibility

      Notclassified

      General Description

      Cyclen is a microcyclic tetramine that can be used as a ligand that forms a co-ordination linkage with the surface metal cations. It can be used as a synthetic precursor. It can be prepared by S-alkylation of dithiooxamide with an excess amount of bromoethane.

      InChI:InChI=1/C8H20N4/c1-2-10-5-6-12-8-7-11-4-3-9-1/h9-12H,1-8H2/p+4

      294-90-6 Relevant articles

      Preparation and animal biodistribution of 166Ho labeled DOTA for possible use in intravascular radiation therapy (IVRT)

      Das, Tapas,Chakraborty, Sudipta,Banerjeel, Sharmila,Samuel, Grace,Sarma,Venkatesh, Meera,Pillai

      , p. 197 - 209 (2003)

      Owing to its favorable decay characteris...

      A copper-cyclen coordination complex associated with a polyoxometalate anion: Synthesis, crystal structure and electrochemistry of [Cu(cyclen)(MeCN)] [W6O19]

      Sarma, Monima,Chatterjee, Tanmay,Das, Samar K.

      , p. 1114 - 1117 (2010)

      The reaction between Cu(NO3)2?3H2O and a...

      Isomerization kinetics of lanthanide(III) complexes with the pendant-arm macrocyclic ligand 1,4,7,10-tetrakis(2-hydroxyethyl)-1,4,7,10-tetraazacyclododecane

      Pittet, Pierre-Andre,Frueh, Dominique,Tissieres, Veronique,Buenzli, Jean-Claude G.

      , p. 895 - 900 (1997)

      The 13C and 1H NMR spectra of the comple...

      A new synthesis of cyclen (1,4,7,10-tetraazacyclododecane)

      Weisman, Gary R.,Reed, David P.

      , p. 5186 - 5187 (1996)

      -

      -

      Kossai,R. et al.

      , p. 1059 - 1062 (1979)

      -

      A practical synthesis of 1,4,7,10-tetraazacyclododecane, a pivotal precursor for MRI contrast agents

      Ferrari, Marinella,Giovenzana, Giovanni B.,Palmisano, Giovanni,Sisti, Massimo

      , p. 15 - 21 (2000)

      A practical preparation of the versatile...

      A microcalorimetric determination of the enthalpies of formation in solution of nickel(II) complexes with tetraaza macrocyclic ligands of varying size

      Fabbrizzi, Luigi,Micheloni, Mauro,Paoletti, Piero

      , p. 535 - 538 (1980)

      The enthalpies of formation of nickel co...

      A new, facile synthesis of 1,4,7,10-tetraazacyclododecane: Cyclen

      Athey, Phillip S.,Kiefer, Garry E.

      , p. 4081 - 4085 (2002)

      This report outlines a new and efficient...

      DINUCLEATING LIGAND OR DINUCLEAR METAL COMPLEX

      -

      Paragraph 0058-0059, (2021/03/19)

      To provide a metal complex that has high...

      Preparation method of cyclen and intermediate thereof

      -

      , (2021/07/08)

      The invention discloses a preparation me...

      Preparation method of cyclen

      -

      Paragraph 0061; 0062; 0063, (2020/02/14)

      The invention provides a preparation met...

      Preparation method of cycleanine

      -

      Paragraph 0031-0050, (2020/02/10)

      The invention provides a preparation met...

      294-90-6 Process route

      C<sub>14</sub>H<sub>24</sub>N<sub>4</sub>

      C14H24N4

      cyclohexane-1,2-dione
      765-87-7

      cyclohexane-1,2-dione

      1,4,7,10-tetraazacyclododecan
      294-90-6

      1,4,7,10-tetraazacyclododecan

      Conditions
      Conditions Yield
      With hydrogenchloride; In water; at 60 ℃; for 6h;
      1,4,7,10-tetraazacyclododecane tetrahydrochloride
      10045-25-7

      1,4,7,10-tetraazacyclododecane tetrahydrochloride

      1,4,7,10-tetraazacyclododecan
      294-90-6

      1,4,7,10-tetraazacyclododecan

      Conditions
      Conditions Yield
      With hydrogenchloride;
      95%
      With potassium hydroxide; In water; at 0 - 10 ℃;
      91.3%
      With potassium hydroxide;
      With sodium hydroxide; In toluene; at 40 ℃; for 1h; Reflux;
      13.77 g
      With sodium hydroxide; In water; toluene;
      12 g

      294-90-6 Upstream products

      • 10045-25-7
        10045-25-7

        1,4,7,10-tetraazacyclododecane tetrahydrochloride

      • 137145-78-9
        137145-78-9

        7-<2-(1,3-Dioxolan-2-yl)ethyl>-1,4,7,10-tetraazacyclododecane-1-carbaldehyde

      • 52667-88-6
        52667-88-6

        cyclen tetratosylate

      • 368864-09-9
        368864-09-9

        cis-octahydro-2a,4a,6a,8a-tetraazacyclopenta[fg]acenaphthylene-3,4-dione

      294-90-6 Downstream products

      • 112193-83-6
        112193-83-6

        1-benzyl-1,4,7,10-tetraazacyclododecane

      • 67705-42-4
        67705-42-4

        1,4,7,10-tetrazatricyclo[5.5.1.0]tridecane

      • 114873-37-9
        114873-37-9

        1,4,7,10-tetraazacyclododecane-1,4,7-triacetic acid

      • 138884-09-0
        138884-09-0

        1,4,7-tribenzyl 1,4,7,10-tetraazacyclododecane 1,4,7-tricarboxylate

      Leave Your Message

      Relevant Products