5,5-Dimethyl-3-oxo-1-cyclohexenyl 4-chlorobenzenecarboxylate

Base Information

• Chemical Name: 5,5-Dimethyl-3-oxo-1-cyclohexenyl 4-chlorobenzenecarboxylate
• CAS No.: 303987-01-1
• Molecular Formula: C15H15ClO3
• Molecular Weight: 278.73100
• DSSTox Substance ID: DTXSID60369706
• Wikidata: Q82156971
• ChEMBL ID: CHEMBL1525194
• Mol file: 303987-01-1.mol

Synonyms:303987-01-1;5,5-dimethyl-3-oxo-1-cyclohexenyl 4-chlorobenzenecarboxylate;(5,5-dimethyl-3-oxocyclohexen-1-yl) 4-chlorobenzoate;5,5-dimethyl-3-oxocyclohex-1-en-1-yl 4-chlorobenzoate;MLS000326693;Benzoic acid, 4-chloro-, 5,5-dimethyl-3-oxo-1-cyclohexen-1-yl ester;SMR000179255;Oprea1_874124;SCHEMBL2027720;CHEMBL1525194;BDBM32847;cid_2732003;DTXSID60369706;HMS2160J03;HMS3309J01;CCG-43224;MFCD00175858;AKOS015991908;CS-0367013;11M-909;SR-01000633160-1;3-(4-chlorobenzoyloxy)-5,5-dimethylcyclo-hexen-1-one;5,5-dimethyl-3-oxocyclohex-1-en-1-yl4-chlorobenzoate;(5,5-dimethyl-3-oxo-cyclohexen-1-yl) 4-chlorobenzoate;(5,5-dimethyl-3-oxidanylidene-cyclohexen-1-yl) 4-chloranylbenzoate;4-chlorobenzoic acid (3-keto-5,5-dimethyl-cyclohexen-1-yl) ester;4-chlorobenzoic acid (5,5-dimethyl-3-oxo-1-cyclohexenyl) ester

Chemical Property of 5,5-Dimethyl-3-oxo-1-cyclohexenyl 4-chlorobenzenecarboxylate

Chemical Property:

• PSA: 43.37000
• LogP: 3.76980
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 278.0709720
• Heavy Atom Count: 19
• Complexity: 404

Purity/Quality:

99% ^*data from raw suppliers

5,5-Dimethyl-3-oxo-1-cyclohexenyl 4-chlorobenzenecarboxylate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(CC(=CC(=O)C1)OC(=O)C2=CC=C(C=C2)Cl)C

Technology Process of 5,5-Dimethyl-3-oxo-1-cyclohexenyl 4-chlorobenzenecarboxylate

There total 1 articles about 5,5-Dimethyl-3-oxo-1-cyclohexenyl 4-chlorobenzenecarboxylate 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: 63.0%

dimedone (126-81-8) + p-chlorobenzoyl isothiocyanate (16794-67-5) → 3-(4-chlorobenzoyloxy)-5,5-dimethyl-2-cyclohexen-1-one (303987-01-1)

Guidance literature:

With potassium hydroxide; In ethanol; for 0.25h;

DOI:10.1023/B:RUJO.0000034955.48174.8f

upstream raw materials:

dimedone

p-chlorobenzoyl isothiocyanate