2-(Methylthio)oxazolo[5,4-c]pyridine

Base Information

Chemical Name:2-(Methylthio)oxazolo[5,4-c]pyridine
CAS No.:169205-96-3
Molecular Formula:C7H6N2OS
Molecular Weight:166.20000
Hs Code.:2934999090
DSSTox Substance ID:DTXSID90437129
Nikkaji Number:J683.683F
Wikidata:Q82252507
Mol file:169205-96-3.mol

Synonyms:2-(Methylthio)oxazolo[5,4-c]pyridine;169205-96-3;2-methylsulfanyl-[1,3]oxazolo[5,4-c]pyridine;2-methylsulfanyl-oxazolo[5,4-c]pyridine;SCHEMBL1018623;DTXSID90437129;DEGNWJBCNBPOPI-UHFFFAOYSA-N;MFCD08447111;AKOS006343926;AS-40626;CS-0328557;FT-0719218;2-(methylsulfanyl)[1,3]oxazolo[5,4-c]pyridine;A882111

Suppliers and Price of 2-(Methylthio)oxazolo[5,4-c]pyridine

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

TRC
2-(Methylthio)oxazolo[5,4-c]pyridine
50mg
$ 45.00

American Custom Chemicals Corporation
2-METHYL SULFANYL-OXAZOLO[5,4-C]PYRIDINE 95.00%
5MG
$ 497.90

Alfa Aesar
2-(Methylthio)oxazolo[5,4-c]pyridine
1g
$ 172.00

Alfa Aesar
2-(Methylthio)oxazolo[5,4-c]pyridine
250mg
$ 44.90

Total 9 raw suppliers

Chemical Property of 2-(Methylthio)oxazolo[5,4-c]pyridine

Chemical Property:

Melting Point:79-81oC
PSA：64.22000
LogP:1.94470
Storage Temp.:2-8°C
XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:166.02008399
Heavy Atom Count:11
Complexity:144

Purity/Quality:

97% ^*data from raw suppliers

2-(Methylthio)oxazolo[5,4-c]pyridine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CSC1=NC2=C(O1)C=NC=C2

Technology Process of 2-(Methylthio)oxazolo[5,4-c]pyridine

There total 5 articles about 2-(Methylthio)oxazolo[5,4-c]pyridine 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: 83.0%

: 169205-98-5
2-Mercaptooxazolo<5,4-c>pyridine

: 74-88-4
methyl iodide

: 169205-96-3
2-(Methylthio)oxazolo<5,4-c>pyridine

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; for 1h;
DOI:10.1021/jo00122a073

Reference yield:

: 52334-53-9
4-amino-3-hydroxy pyridine

: 169205-96-3
2-(Methylthio)oxazolo<5,4-c>pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / ethanol / 18 h / Heating

2: 73 percent / potassium carbonate / dimethylformamide / 1 h

With potassium carbonate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2004.09.010

Reference yield:

: 70298-89-4
4-N-pivaloylaminopyridine

: 169205-96-3
2-(Methylthio)oxazolo<5,4-c>pyridine

Guidance literature:: Multi-step reaction with 4 steps

1: n-BuLi; trimethylborate; H₂O₂

2: HCl; NaOH / H₂O

3: 79 percent / ethanol / 18 h / Heating

4: 73 percent / potassium carbonate / dimethylformamide / 1 h

With hydrogenchloride; sodium hydroxide; n-butyllithium; Trimethyl borate; dihydrogen peroxide; potassium carbonate; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2004.09.010