{[(5-Phenyl-1,3,4-oxadiazol-2-yl)carbamothioyl]sulfanyl}acetic acid

Base Information

Chemical Name:{[(5-Phenyl-1,3,4-oxadiazol-2-yl)carbamothioyl]sulfanyl}acetic acid
CAS No.:62329-40-2
Molecular Formula:C₁₁H₉N₃O₃S₂
Molecular Weight:295.343
Hs Code.:
DSSTox Substance ID:DTXSID60493636
Wikidata:Q82340444

Synonyms:62329-40-2;DTXSID60493636;{[(5-Phenyl-1,3,4-oxadiazol-2-yl)carbamothioyl]sulfanyl}acetic acid

Suppliers and Price of {[(5-Phenyl-1,3,4-oxadiazol-2-yl)carbamothioyl]sulfanyl}acetic acid

Supply Marketing:

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

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Chemical Property of {[(5-Phenyl-1,3,4-oxadiazol-2-yl)carbamothioyl]sulfanyl}acetic acid

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:5
Exact Mass:295.00853350
Heavy Atom Count:19
Complexity:337

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NN=C(O2)NC(=S)SCC(=O)O

Technology Process of {[(5-Phenyl-1,3,4-oxadiazol-2-yl)carbamothioyl]sulfanyl}acetic acid

There total 1 articles about {[(5-Phenyl-1,3,4-oxadiazol-2-yl)carbamothioyl]sulfanyl}acetic acid 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:

: 75-15-0,12122-00-8
carbon disulfide

: 3926-62-3
sodium monochloroacetic acid

: 1574-10-3
benzaldehyde semicarbazone

: 62329-40-2
[(5-phenyl-[1,3,4]oxadiazol-2-yl)-thiocarbamoylsulfanyl]-acetic acid

Guidance literature:: Multistep reaction; (i) Br₂, NaOAc, (ii) /BRN= 1098293/, aq. NH₃, (iii) /BRN= 3597157/, Na₂CO₃;

Reference yield:

: 62329-40-2
[(5-phenyl-[1,3,4]oxadiazol-2-yl)-thiocarbamoylsulfanyl]-acetic acid

: 62329-52-6
5-(4-chloro-benzylidene)-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-2-thioxo-thiazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: Ac₂O

2: piperidine / ethanol

With piperidine; acetic anhydride; In ethanol;

Reference yield:

: 62329-40-2
[(5-phenyl-[1,3,4]oxadiazol-2-yl)-thiocarbamoylsulfanyl]-acetic acid

: 62329-62-8
5-(4-dimethylamino-benzylidene)-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-2-thioxo-thiazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: Ac₂O

2: piperidine / ethanol

With piperidine; acetic anhydride; In ethanol;