[4-(4-methoxyphenyl)-8-methyl-2-oxochromen-7-yl] 3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate

Base Information

Chemical Name:[4-(4-methoxyphenyl)-8-methyl-2-oxochromen-7-yl] 3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
CAS No.:4568-88-1
Molecular Formula:C17H34 O4
Molecular Weight:302.455
Hs Code.:
DSSTox Substance ID:DTXSID70412111

Synonyms:4568-88-1;AC1NR6H5;DTXSID70412111

Suppliers and Price of [4-(4-methoxyphenyl)-8-methyl-2-oxochromen-7-yl] 3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate

Supply Marketing:

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

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of [4-(4-methoxyphenyl)-8-methyl-2-oxochromen-7-yl] 3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate

Chemical Property:

Vapor Pressure:6.77E-25mmHg at 25°C
Boiling Point:789.4°Cat760mmHg
Flash Point:431.2°C
Density:1.286g/cm³
XLogP3:6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:10
Exact Mass:568.22095136
Heavy Atom Count:42
Complexity:1010

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C=CC2=C1OC(=O)C=C2C3=CC=C(C=C3)OC)OC(=O)C(CC4=CNC5=CC=CC=C54)NC(=O)OC(C)(C)C

Technology Process of [4-(4-methoxyphenyl)-8-methyl-2-oxochromen-7-yl] 3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate

There total 11 articles about [4-(4-methoxyphenyl)-8-methyl-2-oxochromen-7-yl] 3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate 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: 94.0%

: 488117-69-7
(S)-14-(2,2-dimethyl-[1,3]dioxolan-4-yl)-tetradecanoic acid methyl ester

: 4568-88-1
(S)-15,16-dihydroxy-hexadecanoic acid methyl ester

Guidance literature:: With acetic acid; In tetrahydrofuran; at 60 ℃; for 5h;
DOI:10.1002/chem.200390021

Reference yield:

: 7735-38-8
13-hydroxytridecanoic acid

: 4568-88-1
(S)-15,16-dihydroxy-hexadecanoic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: HBr; HOAc

2: SOCl₂

3: t-BuOK

4: H₂ / Pd/C / ethanol / 760.05 Torr

5: 94 percent / HOAc / tetrahydrofuran

With thionyl chloride; potassium tert-butylate; hydrogen bromide; hydrogen; acetic acid; palladium on activated charcoal; In tetrahydrofuran; ethanol; 4: Wittig olefination;
DOI:10.1016/j.bmcl.2007.03.084

Reference yield:

: 112-86-7
cis-13-docosenoic acid

: 4568-88-1
(S)-15,16-dihydroxy-hexadecanoic acid methyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: O₃ / ethanol; cyclohexane / 0 - 5 °C

2: KBH₄

3: HBr; HOAc

4: SOCl₂

5: t-BuOK

6: H₂ / Pd/C / ethanol / 760.05 Torr

7: 94 percent / HOAc / tetrahydrofuran

With thionyl chloride; potassium borohydride; potassium tert-butylate; hydrogen bromide; hydrogen; ozone; acetic acid; palladium on activated charcoal; In tetrahydrofuran; ethanol; cyclohexane; 6: Wittig olefination;
DOI:10.1016/j.bmcl.2007.03.084