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2,6-bis(m-nitrobenzylidene)cyclohexan-1-one

  • CasNo:18977-36-1

Product Description

Good factory exports good 2,6-bis(m-nitrobenzylidene)cyclohexan-1-one 18977-36-1

  • Molecular Formula:C20H16N2O5
  • Molecular Weight:364.357
  • Vapor Pressure:4.6E-14mmHg at 25°C 
  • Melting Point:185.6 - 185.9 °C (ethanol) 
  • Boiling Point:593.7°Cat760mmHg 
  • Flash Point:284.4°C 
  • PSA：108.71000 
  • Density:1.389g/cm3 
  • LogP:5.76940 

2,6-bis(m-nitrobenzylidene)cyclohexan-1-one(Cas 18977-36-1) Usage

General Description

2,6-bis(m-nitrobenzylidene)cyclohexan-1-one is a chemical compound with a complex molecular structure. It is a derivative of cyclohexanone, with two m-nitrobenzylidene groups attached to the 2 and 6 positions. 2,6-bis(m-nitrobenzylidene)cyclohexan-1-one is commonly used as a building block in the synthesis of organic molecules and has potential applications in the field of materials science. It exhibits photochromic properties, meaning it can change color when exposed to light, making it useful in the development of light-sensitive materials and devices. The m-nitrobenzylidene groups also make this compound a promising candidate for use in photodynamic therapy and other biomedical applications. Overall, 2,6-bis(m-nitrobenzylidene)cyclohexan-1-one is a versatile and potentially valuable chemical for a range of scientific and industrial purposes.

InChI:InChI=1/C20H16N2O5/c23-20-16(10-14-4-1-8-18(12-14)21(24)25)6-3-7-17(20)11-15-5-2-9-19(13-15)22(26)27/h1-2,4-5,8-13H,3,6-7H2

18977-36-1 Relevant articles

Green, rapid, and highly efficient syntheses of α,α′-bis[(aryl or allyl)idene]cycloalkanones and 2-[(aryl or allyl)idene]-1-indanones as potentially biologic compounds via solvent-free microwave-assisted Claisen–Schmidt condensation catalyzed by MoCl5

Bakhshi, Reza,Zeynizadeh, Behzad,Mousavi, Hossein

, p. 623 - 637 (2019/08/26)

A new, green, and highly efficient proto...

Synthesis of diarylidenecyclohexanone derivatives as potential anti-inflammatory leads against COX-2/mPGES1 and 5-LOX

Kar, Swayamsiddha,Ramamoorthy, Gayathri,Sinha, Shweta,Ramanan, Meera,Pola, Jeevan Kumar,Golakoti, Nageswara Rao,Nanubolu, Jagadeesh Babu,Sahoo, Suraj Kumar,Dandamudi, Rajesh Babu,Doble, Mukesh

supporting information, p. 9012 - 9020 (2019/06/18)

Inflammation is a pathophysiological con...

Synthesis, characterization, crystal structure of novel bis-thiomethylcyclohexanone derivatives and their inhibitory properties against some metabolic enzymes

Bi?er, Abdullah,Taslimi, Parham,Yakal?, Gül,Gül?in, Ilhami,Serdar Gültekin, Mehmet,Turgut Cin, Günseli

, p. 393 - 404 (2018/11/23)

In this study, a series of novel bis-thi...

Synthesis, mechanistic and synergy studies of diarylidenecyclohexanone derivatives as new antiplasmodial pharmacophores

Joshi, Bishnu P.,Mohanakrishnan, Dinesh,Mittal, Garima,Kar, Swayamsiddha,Pola, Jeevan Kumar,Golakoti, Nageswara Rao,Nanubolu, Jagadeesh Babu,D, Rajesh Babu,S, Sai Suraj Kumar,Sahal, Dinkar

, p. 2312 - 2324 (2018/09/20)

Diarylidenecyclohexanone (DAC) derivativ...

18977-36-1 Process route

methyl magnesium iodide
917-64-6

methyl magnesium iodide

cyclohexanol
108-93-0

cyclohexanol

2,6-bis-(3-nitrobenzylidene)cyclohexanone
42792-81-4,18977-36-1

2,6-bis-(3-nitrobenzylidene)cyclohexanone

Conditions
Conditions Yield
anschliessendes Behandeln mit 3-Nitro-benzaldehyd;
2,6-bis-(3-nitrobenzylidene)cyclohexanone
42792-81-4,18977-36-1

2,6-bis-(3-nitrobenzylidene)cyclohexanone

Conditions
Conditions Yield
/BRN= 2061262/;
Cyclohexanon, /BRN= 386795/ / NaOH;
Cyclohexanoncyanhydrin, 1.) HCl-Gas, 2.) m-Nitrobenzaldehyd;
m-Nitrobenzaldehyd, 1.) HCl-Gas, 2.) Cyclohexanoncyanhydrin;
3-Nitro-benzaldehyd, Cyclohexanon, warmes A., 10percentig. NaOH-Lsg. (20grad, 14h);

18977-36-1 Upstream products

  • 108-94-1
    108-94-1

    cyclohexanone

  • 99-61-6
    99-61-6

    3-nitro-benzaldehyde

  • 917-64-6
    917-64-6

    methyl magnesium iodide

  • 108-93-0
    108-93-0

    cyclohexanol

18977-36-1 Downstream products

  • 127249-00-7
    127249-00-7

    2,6-Bis-<(3-aminophenyl)-methylen>-cyclohexanon

  • 129116-66-1
    129116-66-1

    4-(m-nitrophenyl)-8-(m-nitrobenzylidene)-2-imino-5,6,7,8-tetrahydro-4H-3,1-benzothiazine hydrochloride

  • 1222559-16-1
    1222559-16-1

    C31H25N3O7

  • 1353683-10-9
    1353683-10-9

    ethyl 8a-hydroxy-2-methyl-8-(3-nitrobenzylidene)-4-(3-nitrophenyl)-4a,5,6,7,8,8a-hexahydrochromene-3-carboxylate

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