2-OXAZOLECARBONITRILE

2-OXAZOLECARBONITRILE Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: CAS:68776-60-3
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
Tel: +8613580539051
Email: joe@yuhengpharm.com
Products Intro: Product Name:2-oxazolecarbonitrile
CAS:68776-60-3
Purity:0.97 Package:1KG;25KG
Company Name: Golden Pharma Co., Limited
Tel: +undefined18958062155
Email: sales@zjgoldpharm.com
Products Intro: Product Name:2-cyanooxazole
CAS:68776-60-3
Purity:98% Package:100G, 5KG, 25KG or as request Remarks:Commercial stage
Company Name: Shanghai Acmec Biochemical Technology Co., Ltd.
Tel: +86-18621343501; +undefined18621343501
Email: product@acmec-e.com
Products Intro: Product Name:oxazole-2-carbonitrile
CAS:68776-60-3
Purity:95% Package:25g, 1g, 5g, 10g
Company Name: Suzhou ARTK Medchem Co., Ltd.
Tel: +8618118463618
Email: sales1@artkmedchem.com
Products Intro: Product Name:2-oxazolecarbonitrile
CAS:68776-60-3
Purity:0.98 Package:100KG;25KG;10KG;1KG
2-OXAZOLECARBONITRILE Basic information
Product Name:2-OXAZOLECARBONITRILE
Synonyms:2-OXAZOLECARBONITRILE;oxazole-2-carbonitrile;2-CYANO-OXAZOLE;1,3-oxazole-2-carbonitrile
CAS:68776-60-3
MF:C4H2N2O
MW:94.07
EINECS:
Product Categories:
Mol File:68776-60-3.mol
2-OXAZOLECARBONITRILE Structure
2-OXAZOLECARBONITRILE Chemical Properties
Boiling point 165.7±23.0 °C(Predicted)
density 1.25±0.1 g/cm3(Predicted)
storage temp. 2-8°C
pka-3.49±0.10(Predicted)
AppearanceColorless to light yellow Liquid
Safety Information
MSDS Information
2-OXAZOLECARBONITRILE Usage And Synthesis
Synthesis
OXAZOLE-2-CARBOXYLIC ACID AMIDE

884539-45-1

2-OXAZOLECARBONITRILE

68776-60-3

Example 112: Synthesis of 1,3-oxazole-2-carbonitrile; 1,3-oxazole-2-carboxamide (0.98 g, 8.8 mmol, 1.0 eq.) was dissolved in pyridine (17 mL), followed by the addition of phosphorus triclosan (1.2 mL, 12.2 mmol, 1.4 eq.). The reaction mixture was stirred at room temperature for 5 h. The solution was observed to change from a beige slurry to a brown color. After completion of the reaction, the mixture was diluted with ice water and extracted with ether. The aqueous layer was adjusted to pH 3 with 6 M hydrochloric acid and extracted again with ether. The combined ether extracts were washed sequentially with water and saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 1,3-oxazole-2-carbonitrile as an amber colored oil (0.61 g, 74% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 8.608 (s, 1H), 7.67 (s, 1H).

References[1] Patent: WO2006/43145, 2006, A1. Location in patent: Page/Page column 131
[2] Patent: WO2010/45009, 2010, A1. Location in patent: Page/Page column 40-41
[3] Patent: WO2010/45015, 2010, A1. Location in patent: Page/Page column 27
[4] Patent: WO2010/45016, 2010, A1. Location in patent: Page/Page column 20
2-OXAZOLECARBONITRILE Preparation Products And Raw materials
Raw materialsOXAZOLE-2-CARBOXYLIC ACID AMIDE
Tag:2-OXAZOLECARBONITRILE(68776-60-3) Related Product Information
Oxazolo[4,5-c]pyridin-2-amine (9CI) 2-OXAZOLEMETHANOL 5-ISOXAZOLEMETHANOL Oxazolo[4,5-b]pyridine OXAZOLO[4,5-B]PYRIDIN-2(3H)THIONE Oxazole-2-carbaldehyde ETHYL 2-OXAZOLECARBOXYLATE Linezolid Mifepristone 2-OXAZOLECARBONITRILE