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

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​.wat​son​noke​.com/), and here is the cor­re­spond­ing linkhttp://​www​.wat​son​noke​.com/​2​2​-​1​3​-​p​h​e​n​y​l​e​n​e​b​i​s​-​2​-​o​x​a​z​o​l​i​n​e​-​c​a​s​-​3​4​0​5​2​-​9​0​-9/

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