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4-(2-Aminoethyl)benzenesulfonamide

4-(2-Aminoethyl)benzenesulfonamide

CAS Number: 35303-76-5

Molecular Formula: C8H12N2O2S

Purity: 4-(2-Aminoethyl)benzene sulfonamide 98% purity

4-(2-Aminoethyl)benzenesulfonamide priceCAS 35303-76-5 supplierbuy 4-(2-aminoethyl)benzenesulfonamide online99% purity HPLC grademicrofluidic chip research chemicalspharmaceutical building block manufacturer

About 4-(2-Aminoethyl)benzenesulfonamide

4-(2-Aminoethyl)benzene sulfonamide (CAS 35303-76-5) serves as a critical structural component within the API intermediates market, primarily as a high-performance precursor for second-generation sulfonylurea antidiabetics like Glipizide and Gliquidone where high purity fine chemicals (Pharma/API purity 99% | General I...

4-(2-Aminoethyl)benzenesulfonamide Specifications

CAS Number
35303-76-5
Molecular Formula
C8H12N2O2S
Molecular Weight
200.26 g/mol
IUPAC Name
4-(2-aminoethyl)benzenesulfonamide
Canonical SMILES
C1=CC(=CC=C1CCN)S(=O)(=O)N
InChI Key
FXNSVEQMUYPYJS-UHFFFAOYSA-N
InChI
1S/C8H12N2O2S/c9-6-5-7-1-3-8(4-2-7)13(10,11)12/h1-4H,5-6,9H2,(H2,10,11,12)
PubChem CID
169682
EINECS Number
252-501-0
MDL Number
MFCD00010301
HSN No
29359090
Molecular Weight
200.26 g/mol
Purity
4-(2-Aminoethyl)benzene sulfonamide 98% purity
Melting Point
150-152 °C
Boiling Point
387.4±44.0 °C (Predicted)
Freezing point
147.0 to 151.0 °C
Flash Point
188.1 °C
Density
1.2581 (rough estimate)
pKa
10.16±0.10
Precise Quality
35303-76-5
PSA
94.6 Ų
logP
-0.2
Average mass
200.26 g/mol
Monoisotopic mass
200.06194880 Da
Molar mass
200.26 g/mol
Vapour pressure
0 Pa at 25 °C
Safety & Hazard
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Pharmaceutical Intermediate

A key building block utilized in the synthesis and production of various sulfonylurea hypoglycemic drugs and antidiabetic agents, including glipizide, glimepiride, gliquidone, and glibenclamide

Carbonic Anhydrase Inhibitor

A highly selective human carbonic anhydrase (CA) IX inhibitor used in oncology research to study the inhibition of cancer cell growth and the induction of apoptosis in human hepatocellular carcinoma cells

Organic Synthesis Reagent

A functionalized sulfonamide scaffold employed as a starting material or reagent in the development of complex molecules, such as Schiff bases with potential antiviral activity against Zika and Chikungunya viruses, and deorphaning pyrrolopyrazines for antimalarial research

Biochemical Research Tool

A chemical probe used to develop model systems for microfluidic chip implementation and Fourier transform measurements of biochemical interactions, as well as for investigating physiologic functions in cardiovascular system models.

4-(2-Aminoethyl)benzenesulfonamide FAQs

Minimum Order Quantity

25 kg (evaluation) · 1 MT (commercial)

Lead Time

3 – 5 weeks estimated

Delivery Terms

FOB*

Packaging

20 L pails, 200 L HDPE drums, 1000 L IBC

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US SDS · COA · TDS · Specification sheet

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