Methyl 3,4,5-tris(dodecyloxy)benzoate

Base Information

• Chemical Name: Methyl 3,4,5-tris(dodecyloxy)benzoate
• CAS No.: 123126-39-6
• Molecular Formula: C44H80O5
• Molecular Weight: 689.116
• DSSTox Substance ID: DTXSID80572533
• Nikkaji Number: J833.289D
• Wikidata: Q82460909

Synonyms:123126-39-6;METHYL 3,4,5-TRIS(DODECYLOXY)BENZOATE;Benzoic acid, 3,4,5-tris(dodecyloxy)-, methyl ester;SCHEMBL3797840;DTXSID80572533;AHSLFIRTZGMDDL-UHFFFAOYSA-N;Methyl 3,4,5-Tris(dodecanyloxy)benzoate;methyl 3,4,5-tris(n-dodecyloxy) benzoate

Chemical Property of Methyl 3,4,5-tris(dodecyloxy)benzoate

Chemical Property:

• XLogP3: 18.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 38
• Exact Mass: 688.60057565
• Heavy Atom Count: 49
• Complexity: 648

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCOC1=CC(=CC(=C1OCCCCCCCCCCCC)OCCCCCCCCCCCC)C(=O)OC

Technology Process of Methyl 3,4,5-tris(dodecyloxy)benzoate

There total 5 articles about Methyl 3,4,5-tris(dodecyloxy)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%

methyl galloate (99-24-1) + 1-dodecylbromide (143-15-7) → methyl [3,4,5-tris(n-dodecan-1-yloxy)]benzoate (123126-39-6)

Guidance literature:

methyl galloate; With potassium carbonate; In N,N-dimethyl-formamide; at 60 ℃; for 2h;

1-dodecylbromide; In N,N-dimethyl-formamide; at 80 ℃;

DOI:10.1021/ja501277j

Reference yield: 76.0%

methyl galloate (99-24-1) + 1-chlorododecane (112-52-7) → methyl [3,4,5-tris(n-dodecan-1-yloxy)]benzoate (123126-39-6)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 100 ℃; for 12h; Reflux;

DOI:10.1021/cg501697q

Reference yield: 23.0%

methyl galloate (99-24-1) + 1-dodecylbromide (143-15-7) → methyl [3,4,5-tris(n-dodecan-1-yloxy)]benzoate (123126-39-6) + methyl 4-dodecyloxy-3,5-dihydroxybenzoate (477197-46-9) + methyl 3,4-bis(dodecyloxy)-5-hydroxybenzoate (477197-48-1)

Guidance literature:

With sodium hydride; potassium iodide; In N,N-dimethyl-formamide; at 60 ℃;

DOI:10.1016/S0040-4039(02)01101-2

upstream raw materials:

methyl galloate

1-dodecylbromide

3,4,5-trihydroxybenzoic acid

1-chlorododecane

Downstream raw materials:

3,4,5-tridodecyloxy benzoic acid

3,4,5-tris(dodecyloxy)benzyl alcohol

3,4,5-tris(dodecyloxy)benzoic acid hydrazide

2-(3,4,5-trisdodecyloxyphenyl)propan-2-ol

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
  FOB CIF CFR EXW
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 123126-39-6 Benzoic acid, 3,4,5-tris(dodecyloxy)-, methyl ester

Send

Send

Metric Ton KG G Pound L ML

Send

Send