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3-Nitrophenylsulfonylessigsaeure, also known as 3-nitrophenylsulfonyl acetic acid, is an organic compound with the chemical formula C8H7NO6S. It is a derivative of acetic acid, where the hydroxyl group is replaced by a 3-nitrophenylsulfonyl group. 3-Nitrophenylsulfonylessigsaeure is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals and chemical compounds due to its reactive sulfonyl group, which can participate in a range of chemical reactions. The compound's properties, such as its reactivity and stability, make it a valuable building block in organic chemistry and drug development.

3937-95-9

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3937-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3937-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,3 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3937-95:
(6*3)+(5*9)+(4*3)+(3*7)+(2*9)+(1*5)=119
119 % 10 = 9
So 3937-95-9 is a valid CAS Registry Number.

3937-95-9SDS

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 3-Nitrophenylsulfonylessigsaeure

1.2 Other means of identification

Product number -
Other names (3-nitro-benzenesulfonyl)-acetic acid

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

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More Details:3937-95-9 SDS

3937-95-9Relevant academic research and scientific papers

Syntheses of Some Alkyl, Cycloalkyl and Aryl 3-Aminophenyl Sulfones

Courtin, Alfred

, p. 1849 - 1853 (2007/10/02)

Syntheses of alkyl (1a-1i, 1m), cycloalkyl (1j, 1k) and aryl (1l) 3-aminophenyl sulfones were achieved by ethanolic Bechamp-reduction of the appropriate 3-nitrophenyl sulfones (3a-3m).The alkyl (3a-3i) and cycloalkyl (3j, 3k) 3-nitrophenyl sulfones were p

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