Propanoic acid, 3-[(4-formylphenyl)thio]-

Base Information

Chemical Name:Propanoic acid, 3-[(4-formylphenyl)thio]-
CAS No.:88357-10-2
Molecular Formula:C10H10O3S
Molecular Weight:210.254
Hs Code.:
DSSTox Substance ID:DTXSID90474473
Nikkaji Number:J2.342.501G
Wikidata:Q82304507

Synonyms:Propanoic acid, 3-[(4-formylphenyl)thio]-;88357-10-2;SCHEMBL11170850;DTXSID90474473

Suppliers and Price of Propanoic acid, 3-[(4-formylphenyl)thio]-

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 0 raw suppliers

Chemical Property of Propanoic acid, 3-[(4-formylphenyl)thio]-

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:210.03506535
Heavy Atom Count:14
Complexity:198

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C=O)SCCC(=O)O

Technology Process of Propanoic acid, 3-[(4-formylphenyl)thio]-

There total 4 articles about Propanoic acid, 3-[(4-formylphenyl)thio]- 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:

: 141-76-4
3-iodopropanoic acid

: trifluoro-acetic acid 4-formyl-phenylsulfanylmethyl ester

: 88357-10-2
3-<4-Formyl-phenylmercapto>-propionsaeure

Guidance literature:: With TEA; In methanol; at 20 ℃; for 4h;
DOI:10.1016/j.tetlet.2006.04.138

Reference yield:

: 37794-15-3
p-methylsulfinylbenzaldehyde

: 88357-10-2
3-<4-Formyl-phenylmercapto>-propionsaeure

Guidance literature:: Multi-step reaction with 2 steps

1: 2,6-lutidine / various solvent(s) / 0.5 h / 20 °C

2: 5.73 g / TEA / methanol / 4 h / 20 °C

With 2,6-dimethylpyridine; TEA; In methanol; 1: Pummerer rearrangement;
DOI:10.1016/j.tetlet.2006.04.138

Reference yield:

: 3446-89-7
4-(Methylthio)benzaldehyde

: 88357-10-2
3-<4-Formyl-phenylmercapto>-propionsaeure

Guidance literature:: Multi-step reaction with 3 steps

1: 5.5 g / H₂O₂ / 2,2,2-trifluoro-ethanol; CH₂Cl₂; H₂O / 4 h / 20 °C

2: 2,6-lutidine / various solvent(s) / 0.5 h / 20 °C

3: 5.73 g / TEA / methanol / 4 h / 20 °C

With 2,6-dimethylpyridine; TEA; dihydrogen peroxide; In methanol; dichloromethane; 2,2,2-trifluoroethanol; water; 2: Pummerer rearrangement;
DOI:10.1016/j.tetlet.2006.04.138