Contents

Benzisoxazole

Not to be confused with 2,1-Benzisoxazole.

Benzisoxazole

Names
Preferred IUPAC name 1,2-Benzoxazole
Other names Benzo[d]isoxazole; Indoxazine
Identifiers
CAS Number	271-95-4 Y
3D model (JSmol)	Interactive image
Beilstein Reference	2154
ChEBI	CHEBI:51554 Y
ChEMBL	ChEMBL314871 N
ChemSpider	64227 Y
ECHA InfoCard	100.005.440
EC Number	205-983-1
PubChem CID	71073
UNII	D879RKM5NQ Y
CompTox Dashboard (EPA)	DTXSID20181567
InChI InChI=1S/C7H5NO/c1-2-4-7-6(3-1)5-8-9-7/h1-5H Y Key: KTZQTRPPVKQPFO-UHFFFAOYSA-N Y InChI=1/C7H5NO/c1-2-4-7-6(3-1)5-8-9-7/h1-5H Key: KTZQTRPPVKQPFO-UHFFFAOYAI
SMILES n2oc1ccccc1c2
Properties
Chemical formula	C7H5NO
Molar mass	119.123 g·mol−1
Appearance	Colorless liquid
Density	1.18 g/cm3
Boiling point	35 to 38 °C (95 to 100 °F; 308 to 311 K) (at 2.67 hPa) 101-102 °C (at 2 kPa)
Hazards
GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
Flash point	58 °C (136 °F; 331 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

1,2-Benzisoxazole is an aromatic organic compound with a molecular formula C₇H₅NO containing a benzene-fused isoxazole ring structure.^[1][2] The compound itself has no common applications; however, functionalized benzisoxazoles and benzisoxazoyls have a variety of uses, including pharmaceutical drugs such as some antipsychotics (including risperidone, paliperidone, ocaperidone, and iloperidone) and the anticonvulsant zonisamide.

Its aromaticity makes it relatively stable;^[3] however, it is only weakly basic.

Synthesis[edit]

Benzisoxazole may be prepared from inexpensive salicylaldehyde, via a base catalyzed room temperature reaction with hydroxylamine-O-sulfonic acid.^[4]

Reactions[edit]

Kemp elimination[edit]

First reported by Daniel S. Kemp,^[5][6][7] the relatively weak N-O bond can be cleaved by a strong base to yield a 2-hydroxybenzonitrile species.

See also[edit]

Structural isomers

• Benzoxazole
• Anthranil

References[edit]