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assay
98%
form
solid
mp
126-128 °C (lit.)
functional group
ester
SMILES string
COC(=O)c1ccccc1S(N)(=O)=O
InChI
1S/C8H9NO4S/c1-13-8(10)6-4-2-3-5-7(6)14(9,11)12/h2-5H,1H3,(H2,9,11,12)
InChI key
VSOOBQALJVLTBH-UHFFFAOYSA-N
Gene Information
human ... CA1(759) , CA2(760) , CA9(768) , GABRA1(2554)
Application
Methyl 2-(aminosulfonyl)benzoate was used in the preparation of pyrazol-benzenesulfonamides, 2-(1-phenyl-1H-pyrazol-5-yl)benzenesulfonamides.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Preparation of 2-(1-Phenyl-1H-pyrazol-5-yl) benzenesulfonamides from Polylithiated C (alpha), N-Phenylhydrazones and Methyl 2-(Aminosulfonyl) benzoate.
Journal of Heterocyclic Chemistry, 42(6), 1095-1095 (2005)
The Science of the total environment, 721, 137732-137732 (2020-03-17)
The degradation kinetics and residual levels of the sulfonylurea herbicide tribenuron-methyl (TBM) in different environmental waters were studied using in tube-solid phase microextraction (IT-SPME) coupled on-line to nano-liquid chromatography (nanoLC) and UV diode array detection (DAD). This approach combines the
Rapid communications in mass spectrometry : RCM, 29(15), 1370-1380 (2015-07-07)
Sulfonylureas are among the most important class of antidiabetic and herbicides. Solar light excitation and Advanced Oxidation Processes may result in the formation of a wide array of products owing to the relative complex structure. These products, that should be
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