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N-(4-benzylsulfonylphenyl)acetamide is a chemical compound with the molecular formula C15H15NO3S. It is a derivative of acetamide, featuring a benzylsulfonyl group attached to a phenyl ring. N-(4-benzylsulfonylphenyl)acetamide is characterized by its white crystalline appearance and is soluble in organic solvents. It is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure, which can be further modified to create a range of different compounds with specific properties. The compound's reactivity and stability make it a valuable intermediate in the development of new drugs and chemical products.

6305-57-3

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6305-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6305-57-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6305-57:
(6*6)+(5*3)+(4*0)+(3*5)+(2*5)+(1*7)=83
83 % 10 = 3
So 6305-57-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H12FN5O/c16-12-3-1-11(2-4-12)10-21-8-5-14(20-21)19-15(22)13-9-17-6-7-18-13/h1-9H,10H2,(H,19,20,22)

6305-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-[(phenylmethyl)sulfonyl]phenyl]-Acetamide

1.2 Other means of identification

Product number -
Other names Essigsaeure-(4-benzylsulfon-anilid)

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:6305-57-3 SDS

6305-57-3Relevant academic research and scientific papers

The effect of nitrogen atoms in the enantioselective oxidation of aryl or heteroaryl benzyl sulfides

Capozzi, Maria Annunziata M.,Fracchiolla, Giuseppe,Cardellicchio, Cosimo

, p. 646 - 650 (2014/01/06)

Some aminophenyl benzyl sulfides or benzyl pyridyl sulfides were asymmetrically oxidized with tert-butyl hydroperoxide in the presence of a complex between titanium i-propoxide and (S, S)-hydrobenzoin, an oxidation system that works particularly well with

Syntheses of Some Alkyl-, Cycloalkyl-, and Aryl-(4-aminophenyl)-sulfones

Courtin, Alfred

, p. 1046 - 1052 (2007/10/02)

Syntheses of (4-aminophenyl)-alkyl, -cycloalkyl and -aryl sulfones 2 were achieved both by alkylation of 4-(acetylamino)-benzenesulfinic acid (7) to the corresponding acetanilides 9 followed by hydrolysis and by oxidation of the appropriate (4-nitrophenyl)-sulfides 11 to (4-nitrophenyl)-sulfones 1 with subsequent Bechamp reduction.

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