Benzoyl chloride, 4-(nonyloxy)-

Base Information

• Chemical Name: Benzoyl chloride, 4-(nonyloxy)-
• CAS No.: 55768-36-0
• Molecular Formula: C16H23ClO2
• Molecular Weight: 282.81
• DSSTox Substance ID: DTXSID80487153
• Wikidata: Q82329063
• Mol file: 55768-36-0.mol

Synonyms:Benzoyl chloride, 4-(nonyloxy)-;55768-36-0;4-nonyloxybenzoyl chloride;SCHEMBL2399489;DTXSID80487153;YGIQRZYCGUKJRF-UHFFFAOYSA-N;4-(NONYLOXY)BENZOYL CHLORIDE

Chemical Property of Benzoyl chloride, 4-(nonyloxy)-

Chemical Property:

• XLogP3: 6.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 10
• Exact Mass: 282.1386577
• Heavy Atom Count: 19
• Complexity: 235

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCOC1=CC=C(C=C1)C(=O)Cl

Technology Process of Benzoyl chloride, 4-(nonyloxy)-

There total 8 articles about Benzoyl chloride, 4-(nonyloxy)- 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: 100.0%

→ 4-(nonyloxy)benzoyl chloride (55768-36-0)

Guidance literature:

Reference yield:

1-Bromononane (693-58-3) → 4-(nonyloxy)benzoyl chloride (55768-36-0)

Guidance literature:

Multi-step reaction with 2 steps

2: thionyl chloride / 2 h / Heating

With thionyl chloride;

DOI:10.1080/15421408008084015

Reference yield:

methyl 4-hydroxylbenzoate (99-76-3,156291-94-0) → 4-(nonyloxy)benzoyl chloride (55768-36-0)

Guidance literature:

Multi-step reaction with 3 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 20 h / Inert atmosphere; Reflux

2.1: potassium hydroxide / tetrahydrofuran; ethanol; water / Reflux

2.2: 20 °C / Acidic aq. solution

3.1: oxalyl dichloride / dichloromethane / 8 h / 40 °C

With oxalyl dichloride; potassium carbonate; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide;

DOI:10.1080/15421400902841478

upstream raw materials:

1-Bromononane

nonyl alcohol

4-hydroxy-benzoic acid

sel de potassium de l'acide p-hydroxybenzoique

Downstream raw materials:

5-(4-methoxy-phenyl)-2-(4-nonyloxy-phenyl)-thiazole

N-[2-(4-ethoxy-phenyl)-2-oxo-ethyl]-4-nonyloxy-benzamide

3,4-Bis-(4-nonyloxy-benzoyloxy)-benzoic acid

p-thiocyanatophenyl p'-nonyloxybenzoate