3-(Tert-butyl)-4-ethoxybenzaldehyde

Base Information

• Chemical Name: 3-(Tert-butyl)-4-ethoxybenzaldehyde
• CAS No.: 681443-02-7
• Molecular Formula: C13H18O2
• Molecular Weight: 206.28082
• Hs Code.: 2912499000
• DSSTox Substance ID: DTXSID80408747
• Wikidata: Q82214336
• Mol file: 681443-02-7.mol

Synonyms:3-(TERT-BUTYL)-4-ETHOXYBENZALDEHYDE;681443-02-7;3-tert-butyl-4-ethoxybenzaldehyde;BENZALDEHYDE, 3-(1,1-DIMETHYLETHYL)-4-ETHOXY-;DTXSID80408747;AKOS005291340

Chemical Property of 3-(Tert-butyl)-4-ethoxybenzaldehyde

Chemical Property:

• PSA: 26.30000
• LogP: 3.19530
• XLogP3: 3.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 206.130679813
• Heavy Atom Count: 15
• Complexity: 205

Purity/Quality:

98%min ^*data from raw suppliers

3-(tert-Butyl)-4-ethoxybenzaldehyde ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 3-(Tert-butyl)-4-ethoxybenzaldehyde

There total 2 articles about 3-(Tert-butyl)-4-ethoxybenzaldehyde 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:

1-ethoxy-4-methylbenzene (622-60-6) → 4-ethoxy-3-tert-butyl-benzaldehyde (681443-02-7)

Guidance literature:

Multi-step reaction with 2 steps

1: sulfuric acid / 22 - 28 °C

With sulfuric acid;

Reference yield:

2-tert-butyl-4-methyl-phenetole → 4-ethoxy-3-tert-butyl-benzaldehyde (681443-02-7)

Guidance literature:

Reference yield:

4-ethoxy-3-tert-butyl-benzaldehyde (681443-02-7) → 4-ethoxy-3-tert-butyl-benzoic acid

Guidance literature:

DOI:10.1021/jo01144a011

upstream raw materials:

1-ethoxy-4-methylbenzene