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N,N,N-trimethyl(phenylsulfanyl)methanaminium, also known as 1-(phenylthiomethyl)-N,N,N-trimethylmethanaminium, is an organic compound with the chemical formula C11H18NS. It is a quaternary ammonium salt derived from the parent compound, N,N,N-trimethylmethanaminium (also known as trimethylamine), with a phenylsulfanyl group (C6H5SH) attached to the carbon atom. N,N,N-trimethyl(phenylsulfanyl)methanaminium is characterized by its strong electrophilic properties due to the presence of the positively charged nitrogen atom, which makes it a potential reagent in various chemical reactions. It is also known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as in the production of certain dyes and pigments. The compound's structure and properties make it a versatile building block in organic synthesis, with potential uses in the development of new materials and compounds.

6631-73-8

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6631-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6631-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6631-73:
(6*6)+(5*6)+(4*3)+(3*1)+(2*7)+(1*3)=98
98 % 10 = 8
So 6631-73-8 is a valid CAS Registry Number.

6631-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(phenylsulfanylmethyl)azanium,iodide

1.2 Other means of identification

Product number -
Other names trimethyl-(phenylsulfanyl-methyl)-ammonium,iodide

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:6631-73-8 SDS

6631-73-8Downstream Products

6631-73-8Relevant academic research and scientific papers

Synthesis and novel reactivity of halomethyldimethylsulfonium salts

Xu, Yuelian,Fletcher, Michelle,Dolbier Jr., William R.

, p. 3460 - 3465 (2007/10/03)

Iodomethyl-, chloromethyl-, and fluoromethyldimethylsulfonium salts, 4b-d, have been synthesized and are observed to be highly reactive molecules that exhibit extraordinary diversity with respect to the nature of their reactivity, undergoing facile direct substitution (SN2) reactions, but also being highly susceptible to electron-transfer reactions. Cyclic voltametry experiments indicated that the iodomethyldimethylsulfonium compound, 4b, is a potent electron acceptor, even surpassing the reactivity of perfluoro-n-alkyl iodides in that capacity. The iodo- and chloromethyldimethylsulfonium salts, 4b,c, as well as the analogous iodomethyltrimethylammonium salt, 3a, are shown to be reactive SET acceptors.

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