Methyl 3,5-Bis(propargyloxy)benzoate

Base Information

Chemical Name:Methyl 3,5-Bis(propargyloxy)benzoate
CAS No.:768387-51-5
Molecular Formula:C14H12O4
Molecular Weight:244.247
Hs Code.:
DSSTox Substance ID:DTXSID90393716
Nikkaji Number:J2.795.400F
Wikidata:Q82192604
Mol file:768387-51-5.mol

Synonyms:768387-51-5;Methyl 3,5-Bis(propargyloxy)benzoate;Benzoic acid, 3,5-bis(2-propynyloxy)-, methyl ester;methyl 3,5-bis(prop-2-yn-1-yloxy)benzoate;methyl 3,5-bis(prop-2-ynoxy)benzoate;methyl 3,5-bis(2-propynyloxy)benzenecarboxylate;3W-0015;SCHEMBL4279603;DTXSID90393716;LTVUCTGIMYZCJU-UHFFFAOYSA-N;AKOS005090844;methyl3,5-bis(prop-2-yn-1-yloxy)benzoate;3,5-Bis(propargyloxy)benzoic acid methyl ester

Suppliers and Price of Methyl 3,5-Bis(propargyloxy)benzoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
METHYL-3,5-BIS(2-PROPYNYLOXY)BENZENECARBOXYLATE 95.00%
5MG
$ 687.35

American Custom Chemicals Corporation
METHYL-3,5-BIS(2-PROPYNYLOXY)BENZENECARBOXYLATE 95.00%
10MG
$ 679.14

American Custom Chemicals Corporation
METHYL-3,5-BIS(2-PROPYNYLOXY)BENZENECARBOXYLATE 95.00%
1MG
$ 647.61

Total 0 raw suppliers

Chemical Property of Methyl 3,5-Bis(propargyloxy)benzoate

Chemical Property:

PSA：44.76000
LogP:1.49720
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:244.07355886
Heavy Atom Count:18
Complexity:342

Purity/Quality:: METHYL-3,5-BIS(2-PROPYNYLOXY)BENZENECARBOXYLATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)C1=CC(=CC(=C1)OCC#C)OCC#C

Technology Process of Methyl 3,5-Bis(propargyloxy)benzoate

There total 4 articles about Methyl 3,5-Bis(propargyloxy)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: 99.0%

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 106-96-7
propargyl bromide

: 768387-51-5
methyl 3,5-bis(prop-2-ynyloxy)benzoate

Guidance literature:: 1-carbomethoxy-3,5-dihydroxybenzene; With 18-crown-6 ether; potassium carbonate; In tetrahydrofuran; at 20 ℃; for 1h; Inert atmosphere;

propargyl bromide; In tetrahydrofuran; at 65 ℃; for 16h; Inert atmosphere; Enzymatic reaction;
DOI:10.1007/s12039-018-1556-7

Reference yield: 93.0%

: 2150-44-9
1-carbomethoxy-3,5-dihydroxybenzene

: 768387-51-5
methyl 3,5-bis(prop-2-ynyloxy)benzoate

Guidance literature:: 1-carbomethoxy-3,5-dihydroxybenzene; With tetra-(n-butyl)ammonium iodide; potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.0833333h; Inert atmosphere;

propargyl halide, halide = Cl or Br; In N,N-dimethyl-formamide; at 60 ℃; for 18h; Inert atmosphere;
DOI:10.1002/open.201900298