Pharmaceutial Intermediates
  • Ethyl 2-chloroacetoacetate

    • Product Name   :   

      Ethyl 2-chloroacetoacetate

    • CAS No   :   

      609-15-4

    • Project State   :   

      Commercial

    Application

    General Description

    Buy high quality and low price Ethyl 2-chloroacetoacetate 609-15-4 now

    • Molecular Formula:C6H9ClO3
    • Molecular Weight:164.589
    • Appearance/Colour:clear bright yellow liquid 
    • Vapor Pressure:0.086mmHg at 25°C 
    • Melting Point:-80 °C 
    • Refractive Index:n20/D 1.441(lit.)  
    • Boiling Point:225.5 °C at 760 mmHg 
    • PKA:7.92±0.46(Predicted) 
    • Flash Point:50 °C 
    • PSA:43.37000 
    • Density:1.176 g/cm3 
    • LogP:0.74590 

    Ethyl 2-chloroacetoacetate(Cas 609-15-4) Usage

    Biochem/physiol Actions

    Ethyl 2-chloroacetoacetate reacts with thiosemicarbazones to form heterocyclic substituted thiophene derivatives having non-steroidal anti-inflammatory activity.

    InChI:InChI=1/C6H9ClO3/c1-3-10-6(9)5(7)4(2)8/h5H,3H2,1-2H3/t5-/m1/s1

    609-15-4 Relevant articles

    ELECTROCHEMICAL CHLORINATION OF ETHYL ACETOACETATE AND THE FORMATION OF ETHYL 2,2,4-TRICHLOROACETOACETATE

    Ilyushin, V. A.,Malaev, V. G.

    , p. 756 - 757 (1988)

    -

    Synthesis, X-ray crystallographic analysis, DFT studies and biological evaluation of triazolopyrimidines and 2-anilinopyrimidines

    Alsherbiny, Muhammad A.,Canfield, Peter,Fares, Mohamed,Gale, Philip A.,Guang Li, Chun,Jochmans, Dirk,Keller, Paul A.,Lewis, William,Neyts, Johan,Willis, Anthony C.

    , (2021/12/21)

    Inspired by the reported antiviral activ...

    Development of isatin-thiazolo[3,2-a]benzimidazole hybrids as novel CDK2 inhibitors with potent in vitro apoptotic anti-proliferative activity: Synthesis, biological and molecular dynamics investigations

    Eldehna, Wagdy M.,El Hassab, Mahmoud A.,Abo-Ashour, Mahmoud F.,Al-Warhi, Tarfah,Elaasser, Mahmoud M.,Safwat, Nesreen A.,Suliman, Howayda,Ahmed, Marwa F.,Al-Rashood, Sara T.,Abdel-Aziz, Hatem A.,El-Haggar, Radwan

    supporting information, (2021/03/15)

    In the current medical era, human health...

    Design, synthesis, and insecticidal/acaricidal evaluation of novel pyrimidinamine derivatives containing phenyloxazole moiety

    Zhang, Ning,Huang, Ming-Zhi,Liu, Ai-Ping,Liu, Min-Hua,Li, Li-Zhong,Zhou, Chun-Ge,Ren, Ye-Guo,Ou, Xiao-Ming,Long, Chu-Yun,Sun, Jiong,Dang, Ming-Ming,Lan, Zhi-Li

    , p. 963 - 970 (2019/11/03)

    A series of novel pyrimidinamine derivat...

    Pyrimido-pyrrolopyridazine derivative as well as intermediate, preparation method, pharmaceutical composition and application

    -

    Paragraph 0086; 0094-0095, (2020/02/17)

    The invention discloses a pyrimido-pyrro...

    609-15-4 Process route

    ethyl acetoacetate
    141-97-9

    ethyl acetoacetate

    ethyl 2,4-dichloro-3-oxobutanoate
    88-00-6

    ethyl 2,4-dichloro-3-oxobutanoate

    ethyl 2-chloro-3-oxo-butyrate
    609-15-4

    ethyl 2-chloro-3-oxo-butyrate

    Conditions
    Conditions Yield
    With chlorine; at 35 ℃; for 10h; under 750.075 Torr; Product distribution / selectivity;
    ethyl acetoacetate
    141-97-9

    ethyl acetoacetate

    ethyl 2,2-dichloroacetoacetate
    6134-66-3

    ethyl 2,2-dichloroacetoacetate

    ethyl 2-chloro-3-oxo-butyrate
    609-15-4

    ethyl 2-chloro-3-oxo-butyrate

    Conditions
    Conditions Yield
    With potassium peroxymonosulfate; ammonium chloride; In methanol; at 20 ℃; for 6h;
    66 %Chromat.
    12 %Chromat.
    With chloro-trimethyl-silane; [bis(acetoxy)iodo]benzene; In acetonitrile; at 20 ℃; for 2h;

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