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      1,4-Dichlorobutane

      • Product Name: 1,4-Dichlorobutane
      • CAS: 110-56-5
      • Purity:
      • Appearance: Colorless mobile liquid

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      Factory supply good quality 1,4-Dichlorobutane 110-56-5 with stock

      • Molecular Formula:C4H8Cl2
      • Molecular Weight:127.014
      • Appearance/Colour:Colorless mobile liquid 
      • Vapor Pressure:23.7mmHg at 25°C 
      • Melting Point:-38 °C 
      • Refractive Index:n20/D 1.454(lit.)  
      • Boiling Point:153.9 °C at 760 mmHg 
      • Flash Point:40.8 °C 
      • PSA:0.00000 
      • Density:1.16 g/cm3 
      • LogP:2.24420 

      1,4-dichlorobutane(Cas 110-56-5) Usage

      General Description

      1,4-dichlorobutane, also known as 1,4-DCB, is a chemical compound with the formula C4H8Cl2. It is a colorless liquid with a sharp, pungent odor and is insoluble in water but soluble in organic solvents. 1,4-DCB is primarily used as an intermediate in the production of other chemicals, including pharmaceuticals and pesticides. It is also used as a solvent and as a reagent in organic synthesis. The compound is classified as a chlorinated hydrocarbon and is considered to be toxic to the environment, with potential harmful effects on aquatic organisms. It is important to handle and dispose of 1,4-dichlorobutane with care to minimize its impact on human health and the environment.

      InChI:InChI=1/C4H8Cl2/c1-2-3-4(5)6/h4H,2-3H2,1H3

      110-56-5 Relevant articles

      Determination of the hydrogen-bond basicity of weak and multifunctional bases: The case of lindane (γ-hexachlorocyclohexane)

      Ouvrard, Carole,Lucon, Maryvonne,Graton, Jerome,Berthelot, Michel,Laurence, Christian

      , p. 56 - 64 (2004)

      We made use of four methods for determin...

      POLAR RADICALS XVIII. ON THE MECHANISM OF CHLORINATION BY N-CHLOROAMINES: INTERMOLECULAR AND INTRAMOLECULAR ABSTRACTION.

      Tanner, Dennis D.,Arhart, Richard,Meintzer, Christian P.

      , p. 4261 - 4278 (1985)

      The photochlorinations of the n-butyl, n...

      -

      Gunstone,F.D.,Sykes,P.J.

      , p. 3055 - 3058 (1962)

      -

      -

      Dees,Setser

      , p. 2240 (1971)

      -

      Fragmentation of alkoxychlorocarbenes in the gas phase

      Blake, Michael E,Jones Jr., Maitland,Zheng, Fengmei,Moss, Robert A

      , p. 3069 - 3071 (2002)

      In contrast to photolysis or thermal dec...

      -

      Zhulin,Rubinshtein

      , (1976)

      -

      Diels-Alder Reactions of Trichlorophosphaethene

      Teunissen, Herman T.,Hollebeek, Jan,Nieuwenhuizen, Peter J.,Baar, Ben L. M. van,Kanter, Frans J. J. de,Bickelhaupt, Friedrich

      , p. 7439 - 7444 (1995)

      The Diels-Alder reactions of trichloroph...

      -

      Fried,Kleene

      , p. 2691 (1941)

      -

      Solid-phase reactions of alkanedicarboxylic acids with the Pb(OAc) 4-NH4Cl system

      Nikishin, Gennady I.,Sokova, Lyubov L.,Makhaev, Viktor D.,Kapustina, Nadezhda I.

      , p. 264 - 265 (2003)

      The title reactions of HOOC(CH2)nCOOH ac...

      Ethers as Oxygen Donor and Carbon Source in Non-hydrolytic Sol–Gel: One-Pot, Atom-Economic Synthesis of Mesoporous TiO2–Carbon Nanocomposites

      Escamilla-Pérez, Angel Manuel,Louvain, Nicolas,Boury, Bruno,Brun, Nicolas,Mutin, P. Hubert

      , p. 4982 - 4990 (2018)

      Mesoporous TiO2–carbon nanocomposites we...

      Preparation method of dichloroalkane

      -

      Paragraph 0020, (2021/02/10)

      The invention discloses a preparation me...

      Continuous method for preparation of dihalogenated alkane from diol compound

      -

      Paragraph 0051-0054; 0069-0075, (2020/03/16)

      The invention discloses a continuous met...

      Quinoline derivatives and its preparation method and in the application of neural protection in

      -

      Paragraph 0024-0027, (2019/02/19)

      The invention discloses a quinoline deri...

      1,4-dichlorobutane production technology

      -

      Paragraph 0026-0036, (2019/10/23)

      The invention provides a 1,4-dichlorobut...

      110-56-5 Process route

      ethene
      74-85-1

      ethene

      1,2-dichloro-ethane
      107-06-2,52399-93-6

      1,2-dichloro-ethane

      1,2-dichlorobutane
      616-21-7,130232-87-0,130232-88-1

      1,2-dichlorobutane

      1,2-dichlorohexane
      2162-92-7

      1,2-dichlorohexane

      1,2-dichlorooctane
      21948-46-9,72778-28-0

      1,2-dichlorooctane

      1,2-dichlorodecane
      34619-32-4

      1,2-dichlorodecane

      ethylbenzene
      100-41-4,27536-89-6

      ethylbenzene

      1,4-dichlorobutane
      110-56-5

      1,4-dichlorobutane

      Conditions
      Conditions Yield
      With dibenzoyl peroxide; at 100 ℃; Product distribution; Mechanism;
      n-Butyl chloride
      109-69-3

      n-Butyl chloride

      1,1-dichlorobutane
      541-33-3

      1,1-dichlorobutane

      1,3-dichlorobutane
      1190-22-3

      1,3-dichlorobutane

      1,2-dichlorobutane
      616-21-7,130232-87-0,130232-88-1

      1,2-dichlorobutane

      1,4-dichlorobutane
      110-56-5

      1,4-dichlorobutane

      Conditions
      Conditions Yield
      With sulfuryl dichloride; zeolite NaX; for 2h; Heating; Irradiation;
      6 % Chromat.
      23 % Chromat.
      46 % Chromat.
      25 % Chromat.
      With sulfuryl dichloride; zeolite NaX; for 2h; Product distribution; Heating; Irradiation;
      6 % Chromat.
      23 % Chromat.
      46 % Chromat.
      25 % Chromat.
      With norborn-2-ene; N-chlorohexamethyldisilazane; trans-di-O-tert-butyl hyponitrite; at 44.9 ℃; for 1h; Product distribution; Mechanism; further reagent, time;
      With chlorine; In tetrachloromethane; at 20 ℃; Product distribution; other solvents, other temperatures;
      With phenylchloroiodonium chloride; In tetrachloromethane; at 30 ℃; Product distribution; Mechanism; Irradiation; relative rate const., the correlation analysis, subst. phenylchloroiodonium chloride as reagents;
      With N-chloropiperidine; 2,2'-azobis(isobutyronitrile); In trifluoroacetic acid; at 30 ℃; Product distribution; Rate constant; Irradiation; relative rate constants, position selectivity, substrate selectivity;
      With chlorine; In benzene; at -10.1 ℃; Product distribution; dependence of the selectivity of chlorination on the conc. of benzene;
      With N-chloropiperidine; 2,2'-azobis(isobutyronitrile); In trifluoroacetic acid; at 30 ℃; for 3h; Product distribution; Rate constant; Irradiation; other objects - relative reactivities and relative rate constants for the various positions of chlorination;
      With chlorine; In 1,2-dichloro-benzene; at -20 - 50 ℃; Product distribution; Mechanism; Ratio of products and rate constants; different concentrations of o-dichlorobenzene.;
      With chlorine;
      With sulfuryl dichloride; dibenzoyl peroxide;

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        (E)-3-Ureido-but-2-enoic acid ethyl ester

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