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2-Benzoxazolinone

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2-Benzoxazolinone Basic information

Product Name:
2-Benzoxazolinone
Synonyms:
  • USAF ek-5429
  • usafek-5429
  • 2,3-Dihydro-2-oxo-1,3-benzoxazole
  • Benzoxazolin-2-one, 1,3-Benzoxazol-2(3H)-one
  • 2-Benzooazolinone
  • 2-Benzoxazolinone,98%
  • BENZOXAZOLONE (2-BENZOXAZOLINONE)
  • Benzoxazol-2(3H)-one
CAS:
59-49-4
MF:
C7H5NO2
MW:
135.12
EINECS:
200-430-0
Product Categories:
  • Oxazole&Isoxazole
Mol File:
59-49-4.mol
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2-Benzoxazolinone Chemical Properties

Melting point:
137-139 °C(lit.)
Boiling point:
248.79°C (rough estimate)
Density 
1.3124 (rough estimate)
refractive index 
1.5800 (estimate)
Flash point:
160 °C
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
pka
9.50±0.70(Predicted)
form 
Powder
color 
Light beige to brown-gray
Water Solubility 
soluble in hot water
BRN 
119481
InChIKey
ASSKVPFEZFQQNQ-UHFFFAOYSA-N
LogP
1.160
CAS DataBase Reference
59-49-4(CAS DataBase Reference)
NIST Chemistry Reference
Benzoxazolone(59-49-4)
EPA Substance Registry System
2-Benzoxazolinone (59-49-4)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-22-24/25-36/37/38
Safety Statements 
36-24/25-26
RIDADR 
2811
WGK Germany 
3
RTECS 
DM4905000
Hazard Note 
Harmful
TSCA 
Yes
HS Code 
29349990
Toxicity
LD50 orl-rat: 700 mg/kg MDCHAG 4(1),308,64

MSDS

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2-Benzoxazolinone Usage And Synthesis

Chemical Properties

light beige to brown-grey powder. insoluble in water, soluble in benzene, chlorobenzene and other solvents.

Uses

2-Benzoxazolinone is used in the study of the antioxidant activity of heterocyclic chalcones, screening of hydrazines as inhibitors of immune suppressive enzyme indoleamine dioxygenase 1, design and the development of the inhibitors of nitric oxide synthases.

Preparation

2-benzoxazolinone synthesis method: add o-aminophenol, urea and solvent chlorobenzene into the reaction kettle, protect with nitrogen, the reaction temperature is 50~132 ℃, the reaction time is 6h, after the reaction is completed, it is cooled with ice brine, crystallized, Filter the finished product. It is also possible to use o-aminophenol to react with phosgene in the solvent chlorobenzene, quickly pass phosgene within 20 ~ 40 ° C, then heat up to 100 ~ 130 ° C, and then pass phosgene at a lower speed, after the reaction is completed, pass nitrogen to catch up. Phosgene, after work-up, can also obtain 2-benzoxazolinone.

Definition

ChEBI: 2-benzoxazolinone is a member of the class of benzoxazoles that is 2,3-dihydro-1,3-benzoxazole carrying an oxo group at position 2. It has a role as an allelochemical and a phytoalexin.

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 6, p. 123, 1969 DOI: 10.1002/jhet.5570060124
Synthetic Communications, 34, p. 735, 2004 DOI: 10.1081/SCC-120027722
Synthesis, p. 1032, 1983 DOI: 10.1055/s-1983-30616

General Description

2-Benzoxazolinone is a phytoanticipin and its biotransformation by endophytic fungi isolated from Aphelandra tetragona was studied. 2-Benzoxazolinone is a natural chemical produced by rye (Secale cereale) and has strong phytotoxic properties.

Chemical Reactivity

2-benzazolinone is chemically active. in its molecular structure, the hydrogen atom at the 3-position can undergo a methylolation reaction with formaldehyde, and the hydrogen at the 6-position of the benzene ring is easily replaced by chlorine. it is easy to open ring to generate 2-hydroxyphenylamino acid in strong alkaline medium.

Safety Profile

Poison by intraperitoneal route.Moderately toxic by ingestion. When heated todecomposition it emits toxic fumes of NOx.

2-Benzoxazolinone Preparation Products And Raw materials

Raw materials

Preparation Products

2-BenzoxazolinoneSupplier

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