H50802
2-(2-Hydroxyphenyl)benzoxazole
98%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C13H9NO2
CAS Number:
Molecular Weight:
211.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-642-0
MDL number:
Product Name
2-(2-Hydroxyphenyl)benzoxazole, 98%
InChI key
GHGZVWOTJDLREY-UHFFFAOYSA-N
InChI
1S/C13H9NO2/c15-11-7-3-1-5-9(11)13-14-10-6-2-4-8-12(10)16-13/h1-8,15H
SMILES string
Oc1ccccc1-c2nc3ccccc3o2
assay
98%
bp
338 °C (lit.)
mp
122-124 °C (lit.)
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Shang Yanfang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 228, 117746-117746 (2019-11-24)
A 2-oxo-2H-chromene-3-carbohydrazide (CHB) was synthesized by the reaction of salicylaldehyde with diethyl malonate and hydrazine hydrate. The recognition behaviors of CHB to Zn2+ were investigated and the results showed that CHB exhibits well selectivity and sensitivity to Zn2+ with fast
Xue-Jiao Sun et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 228, 117786-117786 (2019-11-20)
A dual-function probe NAHH based on naphthalene was synthesized and characterized. Based on the combination effects derived from the inhabitation of photo-induced electron transfer (PET) and CN isomerization, probe NAHH achieved in the recognition of Zn2+ and Al3+ both through
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service