V900598
磺胺甲基嘧啶
Vetec™, reagent grade, 98%
别名:
4-氨基-N-(4-甲基-2-嘧啶基)苯磺酰胺, N1-(4-甲基嘧啶-2-基)磺胺
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关于此项目
经验公式（希尔记法）:
C11H12N4O2S
化学文摘社编号:
分子量:
264.30
EC Number:
204-866-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
249133
MDL number:
Assay:
98%
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)
InChI key
QPPBRPIAZZHUNT-UHFFFAOYSA-N
SMILES string
Cc1ccnc(NS(=O)(=O)c2ccc(N)cc2)n1
grade
reagent grade
product line
Vetec™
assay
98%
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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
Xian Zhang et al.
Environmental science and pollution research international, 19(5), 1392-1404 (2012-06-30)
Estrogenic compounds and antibiotic residues in environment are receiving significant attention because of their potential adverse effects on ecosystems and human health. The objectives of this study were to determine the occurrence and seasonal variability of eight kinds of estrogenic
Jia Pan et al.
Chemical communications (Cambridge, England), 47(1), 352-354 (2010-08-24)
A phosphine-mediated one-step disulfide formation from S-nitrosothiols has been developed. This reaction can convert unstable S-nitrosothiols to stable disulfides via sulfenamide intermediates under very mild conditions. It has the potential to be used for the detection of S-nitrosothiols.
Kwame W Nti-Addae et al.
Journal of pharmaceutical sciences, 100(3), 1001-1008 (2010-10-20)
Sulfenamide prodrugs of amide and urea functional group containing drugs have recently been proposed as a means of altering the physical and bioproperties of problematic drug molecules containing these two functionalities. Sulfenamides have been shown to revert to the parent
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)
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