2-(Cyclohexylmethyl)-4,6-dimethylbenzaldehyde

Base Information

Chemical Name:2-(Cyclohexylmethyl)-4,6-dimethylbenzaldehyde
CAS No.:119899-40-0
Molecular Formula:C₁₆H₂₂O
Molecular Weight:230.35
Hs Code.:
DSSTox Substance ID:DTXSID201253717

Synonyms:2-(cyclohexylmethyl)-4,6-dimethylbenzaldehyde;119899-40-0;DTXSID201253717

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(Cyclohexylmethyl)-4,6-dimethylbenzaldehyde

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:230.167065321
Heavy Atom Count:17
Complexity:242

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC(=C(C(=C1)CC2CCCCC2)C=O)C

Technology Process of 2-(Cyclohexylmethyl)-4,6-dimethylbenzaldehyde

There total 2 articles about 2-(Cyclohexylmethyl)-4,6-dimethylbenzaldehyde 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:

: 15764-16-6
2,4-dimethylbenzaldehyde

: 119899-40-0
2-(cyclohexylmethyl)-4,6-dimethylbenzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / toluene / 4 h / Heating

2: 1) Pd(OAc)2, 2) PPh₃ / 1) glacial acetic acid, 1.5 h, reflux, 2) toluene, 1 h, 25 deg C

With palladium diacetate; triphenylphosphine; In toluene;

Reference yield:

: 138753-48-7
N-[(2,4-dimethylphenyl)methylene]benzeneamine

: 35166-78-0
cyclohexylmethyl magnesium bromide

: 119899-40-0
2-(cyclohexylmethyl)-4,6-dimethylbenzaldehyde

Guidance literature:: With palladium diacetate; triphenylphosphine; Yield given. Multistep reaction; 1) glacial acetic acid, 1.5 h, reflux, 2) toluene, 1 h, 25 deg C;