Benzoyl chloride, 4-(tetradecyloxy)-

Base Information

• Chemical Name: Benzoyl chloride, 4-(tetradecyloxy)-
• CAS No.: 52244-84-5
• Molecular Formula: C21H33ClO2
• Molecular Weight: 352.945
• DSSTox Substance ID: DTXSID00433955
• Wikidata: Q82248239
• Mol file: 52244-84-5.mol

Synonyms:Benzoyl chloride, 4-(tetradecyloxy)-;52244-84-5;p-tetradecyloxybenzoyl chloride;4-tetradecyloxybenzoyl chloride;SCHEMBL9161795;4(Tetradecyloxy)benzoyl chloride;DTXSID00433955;4-(Tetradecyloxy)benzoyl chloride;QWBDKWSSXVNJKE-UHFFFAOYSA-N

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

Chemical Property:

• XLogP3: 9.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 15
• Exact Mass: 352.2169080
• Heavy Atom Count: 24
• Complexity: 298

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCOC1=CC=C(C=C1)C(=O)Cl

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

There total 11 articles about Benzoyl chloride, 4-(tetradecyloxy)- 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-Bromotetradecane (112-71-0) → 4-tetradecyloxybenzoyl chloride (52244-84-5)

Guidance literature:

Multi-step reaction with 2 steps

1: KOH / ethanol / Heating

2: SOCl₂

With potassium hydroxide; thionyl chloride; In ethanol;

DOI:10.1080/10587250108025027

Reference yield:

oxalyl dichloride (79-37-8) + 4-(tetradecyloxy)benzoic acid (15872-46-5) → 4-tetradecyloxybenzoyl chloride (52244-84-5)

Guidance literature:

In N-methyl-acetamide; diethyl ether; dichloromethane;

Reference yield:

4-hydroxy-benzoic acid (99-96-7) → 4-tetradecyloxybenzoyl chloride (52244-84-5)

Guidance literature:

Multi-step reaction with 2 steps

1: KOH / ethanol / Heating

2: SOCl₂

With potassium hydroxide; thionyl chloride; In ethanol;

DOI:10.1080/10587250108025027

upstream raw materials:

1-Bromotetradecane

4-hydroxy-benzoic acid

1-Tetradecanol

methyl 4-tetradecyloxybenzoate

Downstream raw materials:

N-[2-(2-Pyridinyl)ethyl]-4-(tetradecyloxy)benzamide

[4-(4'-n-tetradecyloxybenzoyloxy)]benzoic acid

4-Tetradecyloxy-benzoic acid 4-formyl-3-hydroxy-phenyl ester

C₆₀H₈₄NO₇