(3H)-OXAZOLONE)

Base Information Edit

Chemical Name:(3H)-OXAZOLONE)
CAS No.:27584-70-9
Molecular Formula:C3H3NO2
Molecular Weight:85.0623
Hs Code.:2934999090
Mol file:27584-70-9.mol

Synonyms:4-Oxazolin-2-one(6CI,7CI,8CI);2-Oxazolone;3H-1,3-Oxazol-2-one;

Suppliers and Price of (3H)-OXAZOLONE)

Supply Marketing:Edit

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-Oxazolone
1g
$ 1260.00

Medical Isotopes, Inc.
2-Oxazolone
1 g
$ 2200.00

Chemenu
Oxazol-2(3H)-one 95%
1g
$ 1075.00

Ambeed
Oxazol-2(3H)-one 95%
1g
$ 1238.00

Ambeed
Oxazol-2(3H)-one 95%
250mg
$ 491.00

Ambeed
Oxazol-2(3H)-one 95%
100mg
$ 311.00

AK Scientific
2(3H)-Oxazolone
5g
$ 3418.00

Total 18 raw suppliers

Chemical Property of (3H)-OXAZOLONE) Edit

Chemical Property:

Vapor Pressure:0.0819mmHg at 25°C
Melting Point:111-113 °C
Refractive Index:1.476
Boiling Point:219.2 °C at 760 mmHg
PKA:9.01±0.20(Predicted)
Flash Point:86.4 °C
PSA：46.00000
Density:1.296 g/cm³
LogP:-0.03210
Storage Temp.:2-8°C

Purity/Quality:

99% ^*data from raw suppliers

2-Oxazolone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 2-Oxazolone is a very useful and versatile tool for synthetic organic chemist. Its derivatives can be used as activating groups in coupling reactions and as efficient and reliable chiral auxiliaries. 2-Oxazolone is also used as a reagent in the synthesis of (±)-8α-hydroxystreptazolone.

Technology Process of (3H)-OXAZOLONE)

There total 11 articles about (3H)-OXAZOLONE) 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: 98.5%

: 27584-70-9
4-oxazolin-2-one

Guidance literature:

Reference yield: 93.0%

: 1432-43-5
3-acetyl-1,3-oxazolidin-2-one

: N-acetyl-4,5-dichloro-2-oxazolidinone

: 27584-70-9
4-oxazolin-2-one

Guidance literature:: With sulfuryl dichloride; In tetrachloromethane; Irradiation;
DOI:10.1055/s-2007-977415

Reference yield: 69.0%

: 100-47-0
benzonitrile

: 98-86-2
acetophenone

: 49746-32-9
N-benzyl-1-phenylethan-1-aminium chloride

Guidance literature:: benzonitrile; acetophenone; With hydrogen; In 2-methyltetrahydrofuran; at 110 ℃; for 20h; under 11251.1 Torr; High pressure; Autoclave;

With hydrogenchloride; In diethyl ether;
DOI:10.1002/chem.202004755