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About This Item
Empirical Formula (Hill Notation):
C11H12N4O2S
CAS Number:
Molecular Weight:
264.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-866-2
Beilstein/REAXYS Number:
249133
MDL number:
Product Name
Sulfamerazine, ReagentPlus®, ≥99.0%
InChI key
QPPBRPIAZZHUNT-UHFFFAOYSA-N
InChI
1S/C11H12N4O2S/c1-8-6-7-13-11(14-8)15-18(16,17)10-4-2-9(12)3-5-10/h2-7H,12H2,1H3,(H,13,14,15)
SMILES string
Cc1ccnc(NS(=O)(=O)c2ccc(N)cc2)n1
product line
ReagentPlus®
assay
≥99.0%
Quality Level
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Related Categories
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Florian M Koch et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(13), 3679-3692 (2011-03-03)
The first catalytic asymmetric synthesis of β-sultones is reported. This development has enabled a rapid access to a number of highly enantioenriched biologically interesting sulfonyl and sulfinyl compound classes, which makes use of the inherent ring strain of the four-membered
Lionel Billiet et al.
Free radical biology & medicine, 52(8), 1473-1485 (2012-02-14)
Protein sulfenic acids are essential cysteine oxidations in cellular signaling pathways. The thermodynamics that drive protein sulfenylation are not entirely clear. Experimentally, sulfenic acid reduction potentials are hard to measure, because of their highly reactive nature. We designed a calculation
Mehdi D Esrafili et al.
Journal of molecular graphics & modelling, 27(3), 326-331 (2008-07-08)
A density functional theory investigation was carried out to characterize (14)N electric field gradient tensors, EFG, in crystalline sulfamerazine and sulfathiazole. To include hydrogen-bonding effects in the calculations, the most probable interacting molecules with the target were considered as tetrameric
Regioselective hydroxysulfenylation of alpha,beta-unsaturated imines: enhanced stability of an intermediate radical.
Masafumi Ueda et al.
Angewandte Chemie (International ed. in English), 47(30), 5600-5604 (2008-06-17)
M S P De Lima et al.
Carbohydrate research, 344(13), 1709-1715 (2009-06-27)
In this work chitosan membranes modified by contact with poly(acrylic acid) (PAA) aqueous solution at two different temperatures (25 degrees C and 60 degrees C) were obtained. The pure chitosan (CS) membranes, as well as those treated with PAA (CSPAA_25
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