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N-(9-oxo-9H-fluoren-4-yl)methanesulfonamide is a chemical compound with the molecular formula C15H13NO3S. It is a derivative of fluorenone, a tricyclic aromatic ketone, and is characterized by the presence of a methanesulfonamide group attached to the fluorenone core. N-(9-oxo-9H-fluoren-4-yl)methanesulfonamide is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is known for its stability and can participate in a range of chemical reactions, making it a valuable building block in organic synthesis. The compound's properties, such as its solubility and reactivity, can be further explored for potential applications in the development of new drugs or chemical products.

7145-73-5

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7145-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7145-73-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7145-73:
(6*7)+(5*1)+(4*4)+(3*5)+(2*7)+(1*3)=95
95 % 10 = 5
So 7145-73-5 is a valid CAS Registry Number.

7145-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(9-oxo-9H-fluoren-4-yl)methanesulfonamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:7145-73-5 SDS

7145-73-5Downstream Products

7145-73-5Relevant academic research and scientific papers

Synthesis and activity of 2-(sulfonamido)methylcarbapenems: Discovery of a novel, anti-MRSA 1,8-naphthosultam pharmacophore

Wilkening,Ratcliffe,Wildonger,Cama,Dykstra,DiNinno,Blizzard,Hammond,Heck,Dorso,St Rose,Kohler,Hammond

, p. 673 - 678 (2007/10/03)

A series of 1β-methyl carbapenems substituted at the 2-position with lipophilic, acyclic and cyclic (sulfonamido)methyl groups was prepared and evaluated for activity against resistant gram-positive bacteria. From these studies, the 1,8-naphthosultamyl gr

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