1-Methylethyl 3,4,5-trimethoxybenzoate

Base Information

Chemical Name:1-Methylethyl 3,4,5-trimethoxybenzoate
CAS No.:6510-89-0
Molecular Formula:C13H18 O5
Molecular Weight:254.283
Hs Code.:2918990090
European Community (EC) Number:229-402-6
UNII:9Y4U6GS3XJ
DSSTox Substance ID:DTXSID50215405
Nikkaji Number:J225.162K
Wikidata:Q83091456
Mol file:6510-89-0.mol

Synonyms:1-Methylethyl 3,4,5-trimethoxybenzoate;6510-89-0;EINECS 229-402-6;propan-2-yl 3,4,5-trimethoxybenzoate;9Y4U6GS3XJ;DTXSID50215405;AKOS008947947;3,4,5-Trimethoxybenzoic acid isopropyl ester;Benzoic acid, 3,4,5-trimethoxy-, 1-methylethyl ester

Suppliers and Price of 1-Methylethyl 3,4,5-trimethoxybenzoate

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

Total 8 raw suppliers

Chemical Property of 1-Methylethyl 3,4,5-trimethoxybenzoate

Chemical Property:

Vapor Pressure:0.000925mmHg at 25°C
Boiling Point:303.5°C at 760 mmHg
Flash Point:128.3°C
PSA：53.99000
Density:1.092g/cm³
LogP:2.27760
XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:254.11542367
Heavy Atom Count:18
Complexity:252

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)OC(=O)C1=CC(=C(C(=C1)OC)OC)OC

Technology Process of 1-Methylethyl 3,4,5-trimethoxybenzoate

There total 3 articles about 1-Methylethyl 3,4,5-trimethoxybenzoate 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: 82.0%

: 86-81-7
3,4,5-trimethoxy-benzaldehyde

: 67-63-0,8013-70-5
isopropyl alcohol

: 6510-89-0
isopropyl 3,4,5-trimethoxybenzoate

Guidance literature:: With 3-mesityl-4-methylthiazol-3-ium bis((trifluoromethyl)sulfonyl)imide; dimethyl sulfoxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; Electrochemical reaction; Inert atmosphere; Flow reactor;
DOI:10.1021/acs.orglett.5b01459