5-(Benzyloxy)-8-chloro-1,4-dimethoxy-2-methylnaphthalene

Base Information

Chemical Name:5-(Benzyloxy)-8-chloro-1,4-dimethoxy-2-methylnaphthalene
CAS No.:89475-09-2
Molecular Formula:C₂₀H₁₉ClO₃
Molecular Weight:342.822
Hs Code.:
DSSTox Substance ID:DTXSID10541611
Wikidata:Q82417998

Synonyms:89475-09-2;5-(Benzyloxy)-8-chloro-1,4-dimethoxy-2-methylnaphthalene;DTXSID10541611

Suppliers and Price of 5-(Benzyloxy)-8-chloro-1,4-dimethoxy-2-methylnaphthalene

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 5-(Benzyloxy)-8-chloro-1,4-dimethoxy-2-methylnaphthalene

Chemical Property:

XLogP3:5.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:342.1022722
Heavy Atom Count:24
Complexity:385

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C2=C(C=CC(=C2C(=C1)OC)OCC3=CC=CC=C3)Cl)OC

Technology Process of 5-(Benzyloxy)-8-chloro-1,4-dimethoxy-2-methylnaphthalene

There total 1 articles about 5-(Benzyloxy)-8-chloro-1,4-dimethoxy-2-methylnaphthalene 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:

: 616-02-4
citraconic acid anhydride

: 106-48-9,82344-39-6
4-chloro-phenol

: 620-05-3
iodomethylbenzene

: 77-78-1
dimethyl sulfate

: 89475-10-5
8-Benzyloxy-5-chlor-4-methoxy-3-methyl-1-naphthol

: 89475-11-6
8-Benzyloxy-5-chlor-1,4-dimethoxy-2-methylnaphthalin

: 89475-09-2
5-Benzyloxy-8-chlor-1,4-dimethoxy-2-methylnaphthalin

Guidance literature:: Yield given. Multistep reaction. Yields of byproduct given;

Reference yield:

: 89475-09-2
5-Benzyloxy-8-chlor-1,4-dimethoxy-2-methylnaphthalin

: 99316-39-9
6-Benzyloxy-5-hydroxy-2-methyl-1,4-naphthochinon

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / sodium acetate, H₂ / Pd/C (10percent Pd) / benzene; methanol / 40 °C / 760 Torr

2: 93 percent / KH₂PO₄, Fremy-salt, 1 N NaOH / H₂O; acetone; ethanol / 0.25 h

3: 69 percent Turnov_. / AlCl₃ / CHCl₃ / ultrasound

4: Ag₂O

With sodium hydroxide; potassium dihydrogenphosphate; aluminium trichloride; potassium nitrososulfonate; hydrogen; sodium acetate; silver(l) oxide; 10% palladium on active carbon; In methanol; ethanol; chloroform; water; acetone; benzene;

Reference yield:

: 89475-09-2
5-Benzyloxy-8-chlor-1,4-dimethoxy-2-methylnaphthalin

: 99316-40-2
6-Benzyloxy-5-methoxy-2-methyl-1,4-naphthochinon

Guidance literature:: Multi-step reaction with 5 steps

1: 99 percent / sodium acetate, H₂ / Pd/C (10percent Pd) / benzene; methanol / 40 °C / 760 Torr

2: 93 percent / KH₂PO₄, Fremy-salt, 1 N NaOH / H₂O; acetone; ethanol / 0.25 h

3: 69 percent Turnov_. / AlCl₃ / CHCl₃ / ultrasound

4: Ag₂O

5: 88 percent / AgO / CHCl₃

With silver(II) oxide; sodium hydroxide; potassium dihydrogenphosphate; aluminium trichloride; potassium nitrososulfonate; hydrogen; sodium acetate; silver(l) oxide; 10% palladium on active carbon; In methanol; ethanol; chloroform; water; acetone; benzene;