159166
1,3-Benzodioxole
99%
Synonym(s):
1,2-(Methylenedioxy)benzene
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About This Item
Empirical Formula (Hill Notation):
C7H6O2
CAS Number:
Molecular Weight:
122.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-992-0
Beilstein/REAXYS Number:
115506
MDL number:
Assay:
99%
Form:
liquid
InChI key
FTNJQNQLEGKTGD-UHFFFAOYSA-N
InChI
1S/C7H6O2/c1-2-4-7-6(3-1)8-5-9-7/h1-4H,5H2
SMILES string
C1Oc2ccccc2O1
vapor pressure
12 mmHg ( 25 °C)
assay
99%
form
liquid
Quality Level
bp
172-173 °C (lit.)
density
1.064 g/mL at 25 °C (lit.)
Related Categories
General description
Supersonic jet fluorescence spectra of 1,3-benzodioxole has been studied. The far-infrared spectrum of the vapour of 1,3-benzodioxole has been reported. The electronic absorption spectra and the laser-induced fluorescence spectra of supersonic-jet-cooled 1,3-benzodioxole molecules has been investigated.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
141.8 °F - closed cup
flash_point_c
61 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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1, 3-benzodioxole: far-infrared spectrum 50-500 cm< sup>- 1</sup>.
Duckett JA, et al.
Chemical Physics Letters, 64(2), 261-265 (1979)
Marie-Josée Haglund Halsør et al.
Scientific reports, 10(1), 11995-11995 (2020-07-21)
Nonulosonic acid (NulO) biosynthesis in bacteria is directed by nab gene clusters that can lead to neuraminic, legionaminic or pseudaminic acids. Analysis of the gene content from a set mainly composed of Aliivibrio salmonicida and Moritella viscosa strains reveals the
Ron Amon et al.
Oncotarget, 8(68), 112236-112244 (2018-01-20)
Humans have circulating antibodies against diverse glycans containing
Supersonic jet fluorescence spectroscopy of 1, 3-benzodioxole: A non-planar (C< sub> 2</sub>) structure in S0.
Hassan KM and Hollas JM.
Chemical Physics Letters, 157(3), 183-188 (1989)
M W Anders et al.
Biochemical pharmacology, 33(4), 577-580 (1984-02-15)
Carbon monoxide is a minor product formed during the cytochrome P-450-catalyzed oxidation of 1,3-benzodioxoles. Studies with [2-13C]methylene 1,3-benzodioxoles established that the methylenic carbon of the 1,3-benzodioxole ring is the source of the carbon atom in the carbon monoxide, and an
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