2,2`-(1,3-Phenylene)bis-2-oxazoline CAS 34052-90-9

2,2`-(1,3-Phenylene)bis-2-oxazoline CAS 34052-90-9

Identification
Properties
Safety Data
Specifications & Other Information
Links

Identification

CAS Number

34052-90-9

Name

2,2`-(1,3-Phenylene)bis-2-oxazoline

Synonyms

m-Phenylene bisoxazoline
2,2′-(1,3-Phenylen)bis(4,5-dihydro-1,3-oxazol) [German] [ACD/IUPAC Name]
2,2′-(1,3-Phenylene)bis(4,5-dihydro-1,3-oxazole) [ACD/IUPAC Name]
2,2′-(1,3-Phénylène)bis(4,5-dihydro-1,3-oxazole) [French] [ACD/IUPAC Name]
2,2′-(m-Phenylene)bis(2-oxazoline)
2-[3-(4,5-Dihydro-1,3-oxazol-2-yl)phenyl]-4,5-dihydro-1,3-oxazole
Oxazole, 2,2′-(1,3-phenylene)bis[4,5-dihydro- [ACD/Index Name]
[34052-90-9]
1,3-bis(2-oxazolin-2-yl)benzene
1,3-bis-(4,5-Dihydro-2-oxazolyl)benzene
1,3-Bis(4,5-dihydro-2-oxazolyl)benzene
1,3-Bis(4,5-dihydrooxazol-2-yl)benzene
1,3-Di-(2-Oxazolin-2-Yl)Benzene
2-(1,3-Phenylene)bis-2-oxazoline
2,2′-(1,3-Phenylene)bis-2-oxazoline
2,2′-(1,3-phenylene)bis-4,5-dihydro-1,3-oxazole
2-[3-(4,5-dihydrooxazol-2-yl)phenyl]-4,5-dihydrooxazole
34052-90-9 [RN]
MFCD00191606

Molecular Structure

Structure of 2,2`-(1,3-Phenylene)bis-2-oxazoline CAS 34052-90-9

Structure of 2,2`-(1,3-Phenylene)bis-2-oxazoline CAS 34052-90-9

SMILES

c1cc(cc(c1)C2=NCCO2)C3=NCCO3

StdInChI

InChI=1S/C12H12N2O2/c1-2-9(11-13-4-6-15-11)8-10(3-1)12-14-5-7-16-12/h1-3,8H,4-7H2

StdInChIKey

HMOZDINWBHMBSQ-UHFFFAOYSA-N

Molecular Formula

C12H12N2O2

Molecular Weight

216.24

Properties

Appearance

White powder

Melting Point

143-146℃

Safety Data

WGK Germany

3

Specifications and Other Information of Our 2,2`-(1,3-Phenylene)bis-2-oxazoline CAS 34052-90-9

Standard

Enterprise standard

Identification Methods

HPLC

Assay

≥98.5%

Residual

≤0.1%m/m

Volatiles

≤0.5%m/m

Package

According to customer requirements to packaging

Manufacturing Capacity

3-4MT/year

Storage

Under the room temperature and away from light

Application

Dioxazoline is an important organic reaction intermediate. Compounds containing two carbon, nitrogen, oxygen, and carbon-nitrogen double-bonded five-membered heterocycles, because of their chemically active nature, can interact with carboxyl, anhydride, amino, epoxy, sulfhydryl, phenolic hydroxyl, iso Cyanate, etc. undergo ring-opening reactions, so dioxazoline can often be used as a chain extender or cross-linker for polymers.

Links

This product is developed by our R&D company Watsonnoke Scientific Ltd(http://www.watsonnoke.com/), and here is the corresponding linkhttp://www.watsonnoke.com/22-13-phenylenebis-2-oxazoline-cas-34052-90-9/

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