6-Methoxy-1-[(2-phenylethoxy)carbonyl]-1H-indole-3-carboxylate

Base Information

Chemical Name:6-Methoxy-1-[(2-phenylethoxy)carbonyl]-1H-indole-3-carboxylate
CAS No.:131424-26-5
Molecular Formula:C₁₉H₁₇NO₅
Molecular Weight:339.348
Hs Code.:2933990090
DSSTox Substance ID:DTXSID60698068
Wikidata:Q82628142
Mol file:131424-26-5.mol

Synonyms:DTXSID60698068;6-Methoxy-1-[(2-phenylethoxy)carbonyl]-1H-indole-3-carboxylate

Suppliers and Price of 6-Methoxy-1-[(2-phenylethoxy)carbonyl]-1H-indole-3-carboxylate

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

American Custom Chemicals Corporation
1-BENZYL-3-METHYL 6-METHOXYINDOLE-1,3-DICARBOXYLATE 95.00%
5MG
$ 500.52

Total 7 raw suppliers

Chemical Property of 6-Methoxy-1-[(2-phenylethoxy)carbonyl]-1H-indole-3-carboxylate

Chemical Property:

Vapor Pressure:1.84E-10mmHg at 25°C
Boiling Point:508.6°C at 760 mmHg
Flash Point:261.4°C
PSA：66.76000
Density:1.22g/cm³
LogP:3.62140
XLogP3:4.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:338.10284761
Heavy Atom Count:25
Complexity:471

Purity/Quality:

98% ^*data from raw suppliers

1-BENZYL-3-METHYL 6-METHOXYINDOLE-1,3-DICARBOXYLATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(C=C1)C(=CN2C(=O)OCCC3=CC=CC=C3)C(=O)[O-]

Technology Process of 6-Methoxy-1-[(2-phenylethoxy)carbonyl]-1H-indole-3-carboxylate

There total 3 articles about 6-Methoxy-1-[(2-phenylethoxy)carbonyl]-1H-indole-3-carboxylate 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: 66.0%

: 131424-25-4
benzyl N-hydroxy-n-(3-methoxyphenyl)carbamate

: 922-67-8
propynoic acid methyl ester

: 131424-26-5
1-benzyl 3-methyl 6-methoxyindole-1,3-dicarboxylate

Guidance literature:: With 4-methyl-morpholine; In dichloromethane; 1) r.t to 40 deg C 2) 1 h;

Reference yield:

: 555-03-3
3-nitroanisole

: 131424-26-5
1-benzyl 3-methyl 6-methoxyindole-1,3-dicarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: Zn, NH₄Cl / ethanol; H₂O

2: K₂CO₃ / diethyl ether; H₂O / 1 h / 0 °C

3: 66 percent / N-methylmorpholine / CH₂Cl₂ / 1) r.t to 40 deg C 2) 1 h

With 4-methyl-morpholine; potassium carbonate; ammonium chloride; zinc; In diethyl ether; ethanol; dichloromethane; water;

Reference yield:

: 24171-80-0
N-(3-methoxyphenyl)hydroxylamine

: 131424-26-5
1-benzyl 3-methyl 6-methoxyindole-1,3-dicarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / diethyl ether; H₂O / 1 h / 0 °C

2: 66 percent / N-methylmorpholine / CH₂Cl₂ / 1) r.t to 40 deg C 2) 1 h

With 4-methyl-morpholine; potassium carbonate; In diethyl ether; dichloromethane; water;