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245232

Sigma-Aldrich

Methyl 2-(aminosulfonyl)benzoate

98%

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About This Item

Linear Formula:
H2NSO2C6H4CO2CH3
CAS Number:
57683-71-3
Molecular Weight:
215.23
EC Number:
260-903-2
MDL number:
MFCD00009808
UNSPSC Code:
12352100
PubChem Substance ID:
24854736
NACRES:
NA.22

Assay

98%

form

solid

mp

126-128 °C (lit.)

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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