1,3-Benzenedicarboxylic acid, 4-(phenylmethoxy)-

Base Information

Chemical Name:1,3-Benzenedicarboxylic acid, 4-(phenylmethoxy)-
CAS No.:63296-13-9
Molecular Formula:C15H12O5
Molecular Weight:272.257
Hs Code.:
DSSTox Substance ID:DTXSID80429210
Nikkaji Number:J2.274.053I
Wikidata:Q82242183

Synonyms:63296-13-9;1,3-Benzenedicarboxylic acid, 4-(phenylmethoxy)-;4-(Benzyloxy)isophthalic acid;4-[(Phenylmethyl)oxy]-1,3-benzenedicarboxylic acid;SCHEMBL1649243;DTXSID80429210;JFILHZCMCBWTRC-UHFFFAOYSA-N

Suppliers and Price of 1,3-Benzenedicarboxylic acid, 4-(phenylmethoxy)-

Supply Marketing:

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

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Chemical Property of 1,3-Benzenedicarboxylic acid, 4-(phenylmethoxy)-

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:272.06847348
Heavy Atom Count:20
Complexity:348

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=C(C=C(C=C2)C(=O)O)C(=O)O

Technology Process of 1,3-Benzenedicarboxylic acid, 4-(phenylmethoxy)-

There total 3 articles about 1,3-Benzenedicarboxylic acid, 4-(phenylmethoxy)- 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:

: 1285516-43-9
bis(phenylmethyl) 4-[(phenylmethyl)oxy]-1,3-benzenedicarboxylate

: 63296-13-9
4-benzyloxy-isophthalic acid

Guidance literature:: bis(phenylmethyl) 4-[(phenylmethyl)oxy]-1,3-benzenedicarboxylate; With water; lithium hydroxide; In tetrahydrofuran; at 20 ℃;

With hydrogenchloride; In tetrahydrofuran; water;

Reference yield:

: 636-46-4
4-hydroxyisophthalic acid

: 63296-13-9
4-benzyloxy-isophthalic acid

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetone / 50 °C

2: water; lithium hydroxide / tetrahydrofuran / 20 °C

With water; potassium carbonate; lithium hydroxide; In tetrahydrofuran; acetone;