Sodium 2-phenyl-1H-indole-5-sulfonate

Name: Sodium 2-phenyl-1H-indole-5-sulfonate
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CAS No. 119205-39-9
Cat. No. CS-0156403
Purity≥95%
MDL No.MFCD04972100

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Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
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Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
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Sodium 2-phenyl-1H-indole-5-sulfonate|CS-0156403

Structure of 119205-39-9

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Description

Dithiooxamide acts as a chelating agent and used in the determination of copper(II), nickel(II) and cobalt(II). It is used as a building block in the synthesis of cyclen. It is involved in the preparation of thiazolothiazole-linked porous organic polymers and N,N'-disubstituted dithiooxamides. It is also employed as a modifier to prepare the modified glassy carbon electrode which is used to investigate the electrochemical properties of quercetin, an important flavonoid derivative. Further, it is involved in the preparation of chelating resin with formaldehyde, which finds application in separation and concentration of silver ions.

General Information

CAS No. 119205-39-9
Cat. No. CS-0156403
Purity ≥95%
MDL No. MFCD04972100
Storage Sealed in dry,2-8℃
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₄H₁₀NNaO₃S
Molecular Weight 295.29
Synonym(s) 2-Phenylindol-5-sulfonic acid,sodium salt
SMILES C1=CC=C(C=C1)C2=CC3=CC(=CC=C3N2)S(=O)(=O)[O-].[Na+]

Computational Chemistry Data

TPSA 72.99
LogP -0.257
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 2

Safety Information

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GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

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Other Classifications

Building Blocks Skeleton Aromatic heterocycle compounds Indole compounds

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Key Words

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Sodium 2-phenyl-1H-indole-5-sulfonate

CAS No. 119205-39-9

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