4-FORMYLPHENYL BENZOATE

Base Information

• Chemical Name: 4-FORMYLPHENYL BENZOATE
• CAS No.: 5339-06-0
• Molecular Formula: C14H10 O3
• Molecular Weight: 226.232
• Hs Code.: 2916310090
• Mol file: 5339-06-0.mol

Synonyms:Benzaldehyde,p-hydroxy-, benzoate (7CI,8CI); 4-(Benzoyloxy)benzaldehyde; 4-Formylphenylbenzoate; NSC 3463; p-(Benzoyloxy)benzaldehyde

Chemical Property of 4-FORMYLPHENYL BENZOATE

Chemical Property:

• Vapor Pressure: 5.32E-06mmHg at 25°C
• Boiling Point: 380.8°Cat760mmHg
• Flash Point: 170.5°C
• PSA: 43.37000
• Density: 1.226g/cm³
• LogP: 2.71830

Purity/Quality:

98%min ^*data from raw suppliers

4-FormylphenylBenzoate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 4-FORMYLPHENYL BENZOATE

There total 21 articles about 4-FORMYLPHENYL BENZOATE 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%

2-(4'-(benzoyloxy)phenyl)-1,3-dithiane → 4-formylphenyl benzoate (5339-06-0)

Guidance literature:

With dihydrogen peroxide; iodine; sodium dodecyl-sulfate; In water; at 20 ℃; for 1h; Micellar solution;

DOI:10.1055/s-0028-1088023

Reference yield: 98.0%

4-hydroxy-benzaldehyde (123-08-0,65581-83-1) + benzoyl chloride (98-88-4) → 4-formylphenyl benzoate (5339-06-0)

Guidance literature:

With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;

DOI:10.1016/j.bmc.2011.09.019

Reference yield: 98.0%

4-hydroxy-benzaldehyde (123-08-0,65581-83-1) + benzoic acid (65-85-0,8013-63-6) → 4-formylphenyl benzoate (5339-06-0)

Guidance literature:

With iodine; triethylamine; triphenylphosphine; In dichloromethane; at 0 - 20 ℃; for 0.333333h;

DOI:10.1016/j.tetlet.2016.03.105

upstream raw materials:

4-hydroxy-benzaldehyde

benzoyl chloride

p-cresyl benzoate

benzoic acid anhydride

Downstream raw materials:

Benzoic acid 4-{[(E)-4-hexadecyloxy-phenylimino]-methyl}-phenyl ester

4-(N-sec-butyliminomethyl)phenyl benzoate

<4-Benzoyloxy-phenyl>-p-tolyl-acetamid

<4-Benzoyloxy-phenyl>-p-tolyl-acetonitril

Refernces

• 1、 Metwally, Nadia Hanafy,Badawy, Mohamed Ahmed,Okpy, Doha Samir. "Green synthesis of some new thiopyrano[2,3-d][1,3]thiazoles using lemon juice and their antibacterial activity". . p. 2496 - 2509. Retrieved 2018.
• 2、 -. "PEROVSKITES FOR PHOTOCATALYTIC ORGANIC SYNTHESIS". . . Retrieved 2022/01/07.
• 3、 Metwally, Nadia Hanafy,Mohamed, Mona Said. "New imidazolone derivatives comprising a benzoate or sulfonamide moiety as anti-inflammatory and antibacterial inhibitors: Design, synthesis, selective COX-2, DHFR and molecular-modeling study". . . Retrieved 2019/12/12.