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N-phenylpropane-1-sulfonamide, also known as N-(1-phenylpropyl)sulfonamide or N-(1-phenylpropyl)benzenesulfonamide, is an organic compound with the chemical formula C9H13NO2S. It is a derivative of propane-1-sulfonamide, featuring a phenyl group attached to the propane chain. N-phenylpropane-1-sulfonamide is a white crystalline solid and is soluble in organic solvents. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. N-phenylpropane-1-sulfonamide is also known for its potential applications in the development of new materials and as a building block in the creation of more complex organic molecules.

6655-25-0

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6655-25-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6655-25-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,5 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6655-25:
(6*6)+(5*6)+(4*5)+(3*5)+(2*2)+(1*5)=110
110 % 10 = 0
So 6655-25-0 is a valid CAS Registry Number.

6655-25-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenylpropane-1-sulfonamide

1.2 Other means of identification

Product number -
Other names Propansulfonsaeureanilid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6655-25-0 SDS

6655-25-0Relevant academic research and scientific papers

1,3,4-OXADIAZOLE SULFONAMIDE DERIVATIVE COMPOUNDS AS HISTONE DEACETYLASE 6 INHIBITOR, AND THE PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

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Paragraph 1219; 1220; 1221, (2017/02/24)

The present invention relates to novel compounds represented by the formula I having histone deacetylase 6 (HDAC6) inhibitory activity, stereoisomers thereof or pharmaceutically acceptable salts thereof, the use thereof for the preparation of therapeutic medicaments, pharmaceutical compositions containing the same, a method for treating diseases using the composition, and methods for preparing the novel compounds. (I) The novel compounds, stereoisomers thereof or pharmaceutically acceptable salts thereof according to the present invention have histone deacetylase (HDAC) inhibitory activity and are effective for the prevention or treatment of HDAC6-mediated diseases.

Low catalyst loadings for ligand-free copper(I)-oxide-catalyzed N-arylation of methanesulfonamide in water

Tan, Bryan Yong-Hao,Teo, Yong-Chua,Seow, Ai-Hua

, p. 1541 - 1546 (2014/03/21)

A simple and practical protocol for the cross-coupling of methanesulfonamide and aryl iodides under ligand-free copper(I)-oxide-catalyzed conditions in water is reported. The method allows the preparation of a wide variety of synthetically useful N-arylated methanesulfonamides in good to excellent yields (up to 90 %) under the optimized conditions. A convenient and efficient ligand-free method using a copper(I) oxide catalyst at 130 °C in water was developed for the N-arylation of methanesulfonamide with aryl iodides. A variety of functionalized aliphatic and cyclic sulfonamides were coupled with different substituted aryl halides to give the corresponding N-arylated products in good to excellent yields under the optimized conditions. Copyright

Low Catalyst Loadings for Ligand-Free Copper(I)-Oxide-Catalyzed N-Arylation of Methanesulfonamide in Water

Tan, Bryan Yong-Hao,Teo, Yong-Chua,Seow, Ai-Hua

, p. 1541 - 1546 (2015/10/05)

A simple and practical protocol for the cross-coupling of methanesulfonamide and aryl iodides under ligand-free copper(I)-oxide-catalyzed conditions in water is reported. The method allows the preparation of a wide variety of synthetically useful N-arylated methanesulfonamides in good to excellent yields (up to 90 %) under the optimized conditions.

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