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245232

Sigma-Aldrich

Methyl 2-(aminosulfonyl)benzoate

98%

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About This Item

Linear Formula:
H2NSO2C6H4CO2CH3
CAS Number:
Molecular Weight:
215.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

Application

Methyl 2-(aminosulfonyl)benzoate was used in the preparation of pyrazol-benzenesulfonamides, 2-(1-phenyl-1H-pyrazol-5-yl)benzenesulfonamides.

pictograms

Exclamation mark

signalword

Warning

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)
P Serra-Mora et al.
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
Rajae Chahboune et al.
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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