218820
Phenoxathiin
97%
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About This Item
Empirical Formula (Hill Notation):
C12H8OS
CAS Number:
Molecular Weight:
200.26
EC Number:
205-975-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
143232
MDL number:
InChI key
GJSGGHOYGKMUPT-UHFFFAOYSA-N
InChI
1S/C12H8OS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8H
SMILES string
O1c2ccccc2Sc3ccccc13
assay
97%
bp
150-152 °C/5 mmHg (lit.)
Gene Information
rat ... Maoa(29253), Maob(25750)
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Aurica Varlan et al.
Molecules (Basel, Switzerland), 15(6), 3905-3919 (2010-07-27)
The interactions of 3-carboxyphenoxathiin with Bovine Serum Albumin (BSA) and Human Serum Albumin (HSA) have been studied by fluorescence and circular dichroism spectroscopy. The binding of 3-carboxyphenoxathiin quenches the BSA and HSA fluorescence, revealing a 1:1 interaction with a binding
A selective, reversible, competitive inhibitor of monoamine oxidase A containing no nitrogen, with negligible potentiation of tyramine-induced blood pressure rise.
M Harfenist et al.
Journal of medicinal chemistry, 34(9), 2931-2933 (1991-09-01)
L J Fitzgerald et al.
Acta crystallographica. Section C, Crystal structure communications, 47 ( Pt 2), 381-385 (1991-02-15)
Mr = 200.25, orthorhombic, P2(1)2(1)2(1), a = 7.758(2), b = 20.506(3), c = 5.896(2) A, V = 938.0(4) A3, Z = 4, Dx = 1.42 g cm-3, lambda(Mo K alpha) = 0.71069 A, mu = 2.88 cm-1, F(000) = 416
H Nojiri et al.
Journal of bacteriology, 181(10), 3105-3113 (1999-05-13)
Carbazole 1,9a-dioxygenase (CARDO) from Pseudomonas sp. strain CA10 is a multicomponent enzyme that catalyzes the angular dioxygenation of carbazole, dibenzofuran, and dibenzo-p-dioxin. It was revealed by gas chromatography-mass spectrometry and 1H and 13C nuclear magnetic resonance analyses that xanthene and
K Stolze et al.
Chemico-biological interactions, 77(3), 283-289 (1991-01-01)
Several derivatives of the phenothiazine cation radicals intercalated into DNA have been investigated using a new flow orientation technique. The anisotropic hyperfine coupling constants of both the parallel and the perpendicular orientation relative to the magnetic field were measured and
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