2,5-Dimethylbenzyl acetate

Base Information

Chemical Name:2,5-Dimethylbenzyl acetate
CAS No.:22184-23-2
Molecular Formula:C11H14O2
Molecular Weight:178.231
Hs Code.:
DSSTox Substance ID:DTXSID701037140
Nikkaji Number:J2.450.531F
Mol file:22184-23-2.mol

Synonyms:2,5-dimethylbenzyl acetate;(2,5-dimethylphenyl)methyl acetate;22184-23-2;SCHEMBL1466758;XDXDSWJZARSVAO-UHFFFAOYSA-N;DTXSID701037140

Suppliers and Price of 2,5-Dimethylbenzyl acetate

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2,5-Dimethylbenzyl acetate

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:178.099379685
Heavy Atom Count:13
Complexity:177

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C=C1)C)COC(=O)C

Technology Process of 2,5-Dimethylbenzyl acetate

There total 7 articles about 2,5-Dimethylbenzyl acetate 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: 93.0%

: 824-45-3
2,5-dimethylbenzyl chloride

: 127-08-2
potassium acetate

: 22184-23-2
2,5-dimethylbenzyl acetate

Guidance literature:: With tetramethylammonium bromide; In acetonitrile; for 18h; Reflux;

Reference yield: 30.0%

: 106-42-3
para-xylene

: 64-19-7,77671-22-8
acetic acid

: 22184-23-2
2,5-dimethylbenzyl acetate

Guidance literature:: With tellurium oxide; lithium bromide; at 118 ℃; for 72h; Product distribution; Mechanism; various alkyl aromatic compounds, various carbonyl compounds, other oxidant;
DOI:10.1021/jo00147a031