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Merck
CN

218820

吩噁噻

97%

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关于此项目

经验公式(希尔记法):
C12H8OS
化学文摘社编号:
分子量:
200.26
EC Number:
205-975-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
143232
MDL number:
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assay

97%

bp

150-152 °C/5 mmHg (lit.)

mp

52-56 °C (lit.)

SMILES string

O1c2ccccc2Sc3ccccc13

InChI

1S/C12H8OS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8H

InChI key

GJSGGHOYGKMUPT-UHFFFAOYSA-N

Gene Information



存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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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
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)
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



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货号GTIN
I3159-10MG04061832924441
I3159-5MG04061833848890
401482-5MG04055977211979