2-(4-Methylphenyl)-3-(naphthalene-1-sulfonyl)-1,3-thiazolidine

Base Information

Chemical Name:2-(4-Methylphenyl)-3-(naphthalene-1-sulfonyl)-1,3-thiazolidine
CAS No.:537678-34-5
Molecular Formula:C20H19NO2S2
Molecular Weight:369.50036
Hs Code.:
DSSTox Substance ID:DTXSID90406794
Mol file:537678-34-5.mol

Synonyms:537678-34-5;Oprea1_419317;Oprea1_425870;DTXSID90406794;2-(4-Methylphenyl)-3-(naphthalene-1-sulfonyl)-1,3-thiazolidine

Suppliers and Price of 2-(4-Methylphenyl)-3-(naphthalene-1-sulfonyl)-1,3-thiazolidine

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
2-(4-METHYLPHENYL)-3-(1-NAPHTHALENYLSULFONYL)-THIAZOLIDINE 95.00%
5MG
$ 504.27

Total 1 raw suppliers

Chemical Property of 2-(4-Methylphenyl)-3-(naphthalene-1-sulfonyl)-1,3-thiazolidine

Chemical Property:

PSA：71.06000
LogP:5.60320
XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:369.08572120
Heavy Atom Count:25
Complexity:551

Purity/Quality:: 2-(4-METHYLPHENYL)-3-(1-NAPHTHALENYLSULFONYL)-THIAZOLIDINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C2N(CCS2)S(=O)(=O)C3=CC=CC4=CC=CC=C43

Technology Process of 2-(4-Methylphenyl)-3-(naphthalene-1-sulfonyl)-1,3-thiazolidine

There total 4 articles about 2-(4-Methylphenyl)-3-(naphthalene-1-sulfonyl)-1,3-thiazolidine 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:

: C₂₀H₂₁NO₂S₂

: 537678-34-5
C₂₀H₁₉NO₂S₂

: 537678-34-5
C₂₀H₁₉NO₂S₂

Guidance literature:: With (R)-AdDIP; sodium phosphate; 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate; In toluene; at 0 ℃; for 48h; Overall yield = 52%; enantioselective reaction;
DOI:10.1002/anie.201711277

Reference yield:

: C₂₀H₂₁NO₂S₂

: 537678-34-5
C₂₀H₁₉NO₂S₂

: 537678-34-5
C₂₀H₁₉NO₂S₂

Guidance literature:: With (R)-AdDIP; sodium phosphate; 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate; In toluene; at 0 ℃; for 48h; Overall yield = 52%; enantioselective reaction;
DOI:10.1002/anie.201711277

Reference yield:

: 106670-34-2
2-(p-methylbenzylthio)-ethylamine

: 537678-34-5
C₂₀H₁₉NO₂S₂

: 537678-34-5
C₂₀H₁₉NO₂S₂

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / chloroform; water / 2 h / 20 °C

2: 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate; sodium phosphate; (R)-AdDIP / toluene / 48 h / 0 °C

With (R)-AdDIP; sodium phosphate; sodium hydroxide; 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate; In chloroform; water; toluene;
DOI:10.1002/anie.201711277