2,2-Bis(4-allyloxyphenyl)propane

Base Information

• Chemical Name: 2,2-Bis(4-allyloxyphenyl)propane
• CAS No.: 3739-67-1
• Molecular Formula: C21H24O2
• Molecular Weight: 308.42
• Hs Code.: 2942000000
• European Community (EC) Number: 223-123-3
• NSC Number: 404194
• UNII: P47L73LDF8
• DSSTox Substance ID: DTXSID30863266
• Nikkaji Number: J205.642I
• Wikidata: Q72446718
• Mol file: 3739-67-1.mol

Synonyms:3739-67-1;2,2-Bis(4-allyloxyphenyl)propane;Bisphenol A bisallyl ether;Bisphenol A diallyl ether;1-prop-2-enoxy-4-[2-(4-prop-2-enoxyphenyl)propan-2-yl]benzene;bisphenol-a diallyl ether;4,4'-(Propane-2,2-diyl)bis((allyloxy)benzene);4,4'-Isopropylidenebis[(allyloxy)benzene];Propane, 2,2-bis(p-(allyloxy)phenyl)-;4,4'-Isopropylidenebis((allyloxy)benzene);EINECS 223-123-3;NSC 404194;NSC-404194;Benzene, 1,1'-(1-methylethylidene)bis[4-(2-propenyloxy)-;Benzene, 1,1'-(1-methylethylidene)bis(4-(2-propen-1-yloxy)-;AI3-02489;Benzene, 1,1'-(1-methylethylidene)bis(4-(2-propenyloxy)-;2,2'-Bis(4-(allyloxy)phenyl)propane;2,2'-Bis[4-(allyloxy)phenyl]propane;Benzene, 1,1'-(1-methylethylidene)bis[4-(2-propen-1-yloxy)-;NSC404194;Matrimid 2292;Homide 126A;BPA-AE;O,O-Diallylbisphenol A;Diallyl ether Bisphenol A;diallylether of bisphenol A;diallyl ether of bisphenol A;SCHEMBL824168;P47L73LDF8;DTXSID30863266;GP-206A;MFCD01218874;Propane,2-bis[p-(allyloxy)phenyl]-;AKOS015995415;BS-52191;CS-0197195;FT-0701323;4,4'-(propane-2,2-diyl)bis(allyloxybenzene);F11442;B-303589;W-109928;Benzene,1'-(1-methylethylidene)bis[4-(2-propenyloxy)-;Benzene, 1,1'-(1-methylethylidene)bis*4-(2-propenyloxy)-;Bisphenol-A diallyl ether;1,1'-(1-Methylethylidene)bis[4-(2-propen-1-yloxy)benzene];1-(Allyloxy)-4-(1-[4-(allyloxy)phenyl]-1-methylethyl)benzene #

Chemical Property of 2,2-Bis(4-allyloxyphenyl)propane

Chemical Property:

• Appearance/Colour: off-yellow liquid
• Vapor Pressure: 3.25E-07mmHg at 25°C
• Refractive Index: 1.536
• Boiling Point: 430.5 °C at 760 mmHg
• Flash Point: 155.3 °C
• PSA: 18.46000
• Density: 1.005 g/cm³
• LogP: 5.14210
• XLogP3: 5.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 8
• Exact Mass: 308.177630004
• Heavy Atom Count: 23
• Complexity: 324

Purity/Quality:

99% ^*data from raw suppliers

4,4'-(Propane-2,2-diyl)bis((allyloxy)benzene) 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C1=CC=C(C=C1)OCC=C)C2=CC=C(C=C2)OCC=C
• Use Description: Bisphenol A bisallyl ether is a chemical compound with various applications across different fields. In the field of polymer chemistry and materials science, it serves as a monomer in the production of epoxy resins and thermosetting plastics. These resins find extensive use in the manufacturing of coatings, adhesives, and composite materials, providing durability and heat resistance to a wide range of products, including automotive parts and electronics. In dentistry, it is employed as a dental composite material, contributing to dental restorations and prosthodontics due to its biocompatibility and mechanical properties. Furthermore, in academic research, it serves as a model compound for studying polymerization reactions and chemical synthesis, advancing our understanding of organic chemistry. Its multifaceted applications underscore its significance in enhancing material performance, dental healthcare, and chemical research across these industries.

Technology Process of 2,2-Bis(4-allyloxyphenyl)propane

There total 17 articles about 2,2-Bis(4-allyloxyphenyl)propane 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: 99.4%

→ bisphenol A diallyl ether (3739-67-1)

Guidance literature:

Reference yield: 99.0%

BPA (80-05-7) + allyl bromide (106-95-6) → bisphenol A diallyl ether (3739-67-1)

Guidance literature:

BPA; With potassium carbonate; In acetone; for 1h; Inert atmosphere; Reflux;

allyl bromide; In acetone; Reflux; Inert atmosphere;

DOI:10.3762/bjoc.10.180

Reference yield: 98.0%

BPA (80-05-7) + 3-chloroprop-1-ene (107-05-1) → bisphenol A diallyl ether (3739-67-1)

Guidance literature:

With potassium carbonate; sodium iodide; In ethanol; for 24h; Heating;

DOI:10.1021/jo961815m

upstream raw materials:

BPA

allyl bromide

3-chloroprop-1-ene

allyl methyl carbonate

Downstream raw materials:

2,2-bis(3-allyl-4-hydroxyphenyl)propane

4,4'-isopropylidenediphenol dipropyl ether

C₂₁H₂₄O₄

2,2',6,6'-tetraallyl-4,4'-isopropylidenediphenol

Refernces

• 1、 -. "COMPOUND, CURABLE COMPOSITION INCLUDING THE SAME AND CROSSLINKING AGENT FOR CURABLE COMPOSITION". Paragraph 0049-0050. . Retrieved 2021/07/17.
• 2、 -. "THERMOSETTING ALKOXYSILYL COMPOUND HAVING TWO OR MORE ALKOXYSILYL GROUPS, COMPOSITION AND CURED PRODUCT COMPRISING SAME, USE THEREOF, AND METHOD FOR PREPARING ALKOXYSILYL COMPOUND". Paragraph 0378; 0379; 0382; 0469; 0478. . Retrieved 2018/06/15.