1H-Indole-3-carboxaldehyde, 6-methoxy-1-(phenylsulfonyl)-

Base Information

Chemical Name:1H-Indole-3-carboxaldehyde, 6-methoxy-1-(phenylsulfonyl)-
CAS No.:143702-30-1
Molecular Formula:C16H13NO4S
Molecular Weight:315.35
Hs Code.:
DSSTox Substance ID:DTXSID00437296
Nikkaji Number:J1.907.715B
Wikidata:Q82252776
Mol file:143702-30-1.mol

Synonyms:143702-30-1;6-methoxy-1-(phenylsulfonyl)-1H-indole-3-carbaldehyde;1H-Indole-3-carboxaldehyde, 6-methoxy-1-(phenylsulfonyl)-;DTXSID00437296;1-(benzenesulfonyl)-6-methoxy-1H-indole-3-carbaldehyde;1-(Phenylsulfonyl)-6-methoxy-1H-indole-3-carbaldehyde

Suppliers and Price of 1H-Indole-3-carboxaldehyde, 6-methoxy-1-(phenylsulfonyl)-

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

Total 3 raw suppliers

Chemical Property of 1H-Indole-3-carboxaldehyde, 6-methoxy-1-(phenylsulfonyl)-

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:315.05652907
Heavy Atom Count:22
Complexity:495

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(C=C1)C(=CN2S(=O)(=O)C3=CC=CC=C3)C=O

Technology Process of 1H-Indole-3-carboxaldehyde, 6-methoxy-1-(phenylsulfonyl)-

There total 6 articles about 1H-Indole-3-carboxaldehyde, 6-methoxy-1-(phenylsulfonyl)- 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:

: 16732-73-3
6-Methoxyindole-2-carboxylic acid

: 143702-30-1
6-methoxy-1-(phenylsulfonyl)-1H-indole-3-carbaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1: 97.6 percent / Cu / quinoline / 2 h / Heating

2: 1.) POCl₃, 3.) aq. NaOH

3: 1.) NaH / 1.) THF, 40 deg C, 90 min, 2.) THF, RT, 18 h

With sodium hydroxide; copper; sodium hydride; trichlorophosphate; In quinoline;
DOI:10.1080/00397919208021343

Reference yield:

: 98081-83-5
methyl 6-methoxy-1H-indole-2-carboxylate

: 143702-30-1
6-methoxy-1-(phenylsulfonyl)-1H-indole-3-carbaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1: 93.9 percent / 2N aq. NaOH / 0.5 h / Heating

2: 97.6 percent / Cu / quinoline / 2 h / Heating

3: 1.) POCl₃, 3.) aq. NaOH

4: 1.) NaH / 1.) THF, 40 deg C, 90 min, 2.) THF, RT, 18 h

With sodium hydroxide; copper; sodium hydride; trichlorophosphate; In quinoline;
DOI:10.1080/00397919208021343

Reference yield:

: 143702-29-8
2-azido-3-(4'-methoxyphenyl)acrylic acid methyl ester

: 143702-30-1
6-methoxy-1-(phenylsulfonyl)-1H-indole-3-carbaldehyde

Guidance literature:: Multi-step reaction with 5 steps

1: 89 percent / xylene / 9 h / Heating

2: 93.9 percent / 2N aq. NaOH / 0.5 h / Heating

3: 97.6 percent / Cu / quinoline / 2 h / Heating

4: 1.) POCl₃, 3.) aq. NaOH

5: 1.) NaH / 1.) THF, 40 deg C, 90 min, 2.) THF, RT, 18 h

With sodium hydroxide; copper; sodium hydride; trichlorophosphate; In quinoline; xylene;
DOI:10.1080/00397919208021343