Cyclopropyl 4-ethoxyphenyl ketone

Base Information

• Chemical Name: Cyclopropyl 4-ethoxyphenyl ketone
• CAS No.: 75343-44-1
• Molecular Formula: C12H14 O2
• Molecular Weight: 190.242
• DSSTox Substance ID: DTXSID20392575
• Wikidata: Q82190922
• Mol file: 75343-44-1.mol

Synonyms:Cyclopropyl 4-ethoxyphenyl ketone;75343-44-1;Cyclopropyl-(4-ethoxyphenyl)methanone;SCHEMBL9156027;DTXSID20392575;GLZVGOOXNYUJMW-UHFFFAOYSA-N;cyclopropyl (4-ethoxyphenyl) ketone;AKOS000346069;Cyclopropyl 4-ethoxyphenyl ketone, 98%;CYCLOPROPYL(4-ETHOXYPHENYL)METHANONE

Chemical Property of Cyclopropyl 4-ethoxyphenyl ketone

Chemical Property:

• Melting Point: 67-69 °C(lit.)
• PSA: 26.30000
• LogP: 2.67800
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 190.099379685
• Heavy Atom Count: 14
• Complexity: 200

Purity/Quality:

Cyclopropyl 4-ethoxyphenyl ketone 98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC1=CC=C(C=C1)C(=O)C2CC2

Technology Process of Cyclopropyl 4-ethoxyphenyl ketone

There total 3 articles about Cyclopropyl 4-ethoxyphenyl ketone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 82.0%

4-chloro-1-(4-ethoxyphenyl)butan-1-one (75343-08-7) → cyclopropyl (4-ethoxyphenyl)-methanone (75343-44-1)

Guidance literature:

With potassium hydroxide; In methanol; cooling to 20 deg C;

Reference yield:

cyclopropanecarboxylic acid chloride (4023-34-1) + Phenetole (103-73-1) → cyclopropyl (4-ethoxyphenyl)-methanone (75343-44-1)

Guidance literature:

aluminium trichloride; In carbon disulfide; dichloromethane; water; Petroleum ether;

Reference yield:

Phenetole (103-73-1) + 4-Chlorobutanoyl chloride (4635-59-0) → cyclopropyl (4-ethoxyphenyl)-methanone (75343-44-1)

Guidance literature:

With aluminium trichloride; anschliessend mit methanol.KOH;

DOI:10.1021/ja01563a049

upstream raw materials:

Phenetole

4-Chlorobutanoyl chloride

4-chloro-1-(4-ethoxyphenyl)butan-1-one

cyclopropanecarboxylic acid chloride

Downstream raw materials:

methyl 4-cyclopropyl4-(4-ethoxyphenyl)-2-fluorobut-2-enoate

2,2,4-Tribromo-1-(3-bromo-4-ethoxy-phenyl)-butan-1-one

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