5-oxazolmethyl cyanide

Base Information

Chemical Name:5-oxazolmethyl cyanide
CAS No.:947771-07-5
Molecular Formula:C₅H₄N₂O
Molecular Weight:108.1
Hs Code.:2934999090
Mol file:947771-07-5.mol

Synonyms:1,3-OXAZOL-5-YLACETONITRILE;

Suppliers and Price of 5-oxazolmethyl cyanide

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

AK Scientific
1,3-Oxazol-5-ylacetonitrile
1g
$ 1207.00

Total 4 raw suppliers

Chemical Property of 5-oxazolmethyl cyanide

Chemical Property:

Boiling Point:231.5±15.0 °C (760 mmHg)
PSA：49.82000
Density:1.179±0.06 g/cm3 (20 °C, 760 mmHg)
LogP:0.74068

Purity/Quality:

97% ^*data from raw suppliers

1,3-Oxazol-5-ylacetonitrile ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 5-oxazolmethyl cyanide

There total 2 articles about 5-oxazolmethyl cyanide 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:

: 773837-37-9
sodium cyanide

: 172649-57-9
5-(chloromethyl)oxazole

: 947771-07-5
2-(oxazol-5-yl)acetonitrile

Guidance literature:: In N,N-dimethyl-formamide; at 20 - 70 ℃; for 4h; Inert atmosphere;

Reference yield:

: 172649-57-9
5-(chloromethyl)oxazole

: 143-33-9,25596-52-5
sodium cyanide

: 947771-07-5
2-(oxazol-5-yl)acetonitrile

Guidance literature:: In N,N-dimethyl-formamide; at 70 ℃; for 2.5h;
DOI:10.1002/chem.200700033

Reference yield:

: 947771-07-5
2-(oxazol-5-yl)acetonitrile

: C₁₆H₁₄F₃NO₆

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / HCl / 13 h / Heating

2: LiHMDS; 5,5-(MeO)2-6,10-N-SO₂-6,N-oxo-bornane / tetrahydrofuran / 0.5 h / -78 °C

3: DMAP / tetrahydrofuran / 2 h / 20 °C

With hydrogenchloride; dmap; lithium hexamethyldisilazane; In tetrahydrofuran;
DOI:10.1002/chem.200700033