4-HYDROXY-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER

Base Information

Chemical Name:4-HYDROXY-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER
CAS No.:13041-63-9
Molecular Formula:C₁₂H₁₀O₃
Molecular Weight:202.21
Hs Code.:2918290000
Mol file:13041-63-9.mol

Synonyms:1-Naphthoicacid, 4-hydroxy-, methyl ester (6CI,7CI,8CI); Methyl 4-hydroxy-1-naphthoate

Suppliers and Price of 4-HYDROXY-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER

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

Alichem
Methyl4-naphthol-1-carboxylate
1g
$ 1769.25

Alichem
Methyl4-naphthol-1-carboxylate
500mg
$ 970.20

Alichem
Methyl4-naphthol-1-carboxylate
250mg
$ 727.60

AK Scientific
Methyl4-hydroxy-1-naphthoate
1g
$ 622.40

Total 7 raw suppliers

Chemical Property of 4-HYDROXY-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER

Chemical Property:

PSA：46.53000
LogP:2.33200

Purity/Quality:

99% ^*data from raw suppliers

Methyl4-naphthol-1-carboxylate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4-HYDROXY-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER

There total 2 articles about 4-HYDROXY-NAPHTHALENE-1-CARBOXYLIC ACID METHYL ESTER 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: 68.0%

: C₁₂H₁₀O₃

: 947-65-9
methyl 2-hydroxy-1-naphthoate

: 13041-63-9
1-(4-hydroxynaphthyl)methanoate

Guidance literature:: With dichlorotricarbonylruthenium(II) dimer; In 1,2-dichloro-ethane; at 80 ℃; for 72h; regioselective reaction; Inert atmosphere;
DOI:10.1021/jo901504n

Reference yield:

: 83164-95-8
1-carbomethoxy-11-oxatricyclo[6.2.1.0^2,7]undeca-2,4,6,9-tetraene

: 947-65-9
methyl 2-hydroxy-1-naphthoate

: 13041-63-9
1-(4-hydroxynaphthyl)methanoate

Guidance literature:: With chloro(1,5-cyclooctadiene)(pentamethylcyclopentadiene)ruthenium(II); In tetrahydrofuran; Darkness; Inert atmosphere;
DOI:10.1002/ejoc.200800424