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N-(dibenzyl-lambda~4~-sulfanylidene)-4-methylbenzenesulfonamide is a complex organic chemical compound with the molecular formula C21H21NO2S2. It features a benzenesulfonamide core, which is a derivative of benzenesulfonamide, with a 4-methyl substitution. The compound is characterized by a dibenzyl-sulfanylidene group (lambda~4~-sulfanylidene) attached to the nitrogen atom, which introduces a unique sulfur-based structure. This specific arrangement of atoms and functional groups may confer distinct chemical properties and reactivity, potentially useful in various chemical and pharmaceutical applications. The compound's structure and properties make it a subject of interest for researchers in organic synthesis and medicinal chemistry.

3249-66-9

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3249-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3249-66-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,4 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3249-66:
(6*3)+(5*2)+(4*4)+(3*9)+(2*6)+(1*6)=89
89 % 10 = 9
So 3249-66-9 is a valid CAS Registry Number.
InChI:InChI=1/C21H21NO2S2/c1-18-12-14-21(15-13-18)26(23,24)22-25(16-19-8-4-2-5-9-19)17-20-10-6-3-7-11-20/h2-15H,16-17H2,1H3

3249-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name S,S-Dibenzyl-N-(toluol-4-sulfonyl)-sulfimid

1.2 Other means of identification

Product number -
Other names dibenzyl methylmalonate

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:3249-66-9 SDS

3249-66-9Relevant academic research and scientific papers

Sulfonylimino group transfer reaction using imino-λ3-iodanes with I2 as catalyst under metal-free conditions

Yoshimura, Akira,Makitalo, Cody L.,Jarvi, Melissa E.,Shea, Michael T.,Postnikov, Pavel S.,Rohde, Gregory T.,Zhdankin, Viktor V.,Saito, Akio,Yusubov, Mekhman S.

, (2019/03/19)

A new practical procedure of imination for sulfide has been developed. The treatment of (N-tosylimino)-phenyl-λ3-iodane, PhINTs, with various sulfides in the presence of a catalytic amount of I2 under metal-free conditions affords the corresponding N-tosylsulfilimine compounds with moderate to good yields. This facile transfer procedure of the sulfonylimino group can also be applied to triphenylphosphine to produce the respective iminotriphenylphosphoranes in high yields. According to the reaction mechanism studies, the process of imination from (N-tosylimino)-phenyl-λ3-iodane to sulfide under the conditions may involve radical steps within the reaction mechanism.

A simple method for the preparation of N-sulfonylsulfilimines from sulfides

Marzinzik,Sharpless

, p. 594 - 596 (2007/10/03)

While excellent methods exist for the oxidation of sulfides to sulfoxides R1R2S → R1R2SO, the aza-version of this atom transfer redox process, i.e., R1R2S → R1R2S=N-SO

Hypervalent iodine in synthesis XXXII: A novel way for the synthesis of N-sulfonylsulfilimines from sulfides and sulfonamides using iodosobenzene diacetate

Ou, Wei,Chen, Zhen-Chu

, p. 4443 - 4449 (2007/10/03)

A number of N-sulfonylsulfilimines have been prepared through a novel way for the reaction of iodosobenzene diacetate with sulfides and sulfonamides under mild conditions.

PREPARATION OF TETRAALKYLAMMONIUM N-CHLORO-p-TOLUENESULFONAMIDES AND THEIR APPLICATION TO IMINATION OF PHOSPHORUS COMPOUNDS AND SULFIDES.

Yamamoto,Yoshida,Hojyo,Terauchi

, p. 3341 - 3342 (2007/10/02)

Tetraalkylammonium N-chloro-p-toluenesulfonamides were prepared from chloramine T and tetraalkylammonium chlorides as a substance corresponding to anhydrous chloramine T, and found to give rise to the effective tosylimination of phosphorus compounds and d

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