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53136-21-3

BENZYL 4-BROMOPHENYL SULFIDE

Catalog#: AR003EPQ  |   CAS#: 53136-21-3  |   MDL#: MFCD00028019  |   MF: C13H11BrS  |   MW: 279.1954

Packsize Purity Price Availability Quantity
100mg 98% $15.00 Global Stock Buy Now Add To Cart
250mg 98% $23.00 Global Stock Buy Now Add To Cart
1g 98% $47.00 Global Stock Buy Now Add To Cart
5g 98% $160.00 Global Stock Buy Now Add To Cart
10g 98% $319.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003EPQ
Chemical Name BENZYL 4-BROMOPHENYL SULFIDE
CAS Number 53136-21-3
Molecular Formula C13H11BrS
Molecular Weight 279.1954
MDL Number MFCD00028019
SMILES Brc1ccc(cc1)SCc1ccccc1

The benzyl(4-bromophenyl)sulfane compound is a valuable reagent in chemical synthesis due to its ability to participate in a variety of reactions, leading to the formation of new organic compounds with unique properties. This particular compound has found widespread application in organic synthesis as a versatile building block for the construction of more complex molecules.One key application of benzyl(4-bromophenyl)sulfane is its use as a sulfenylating agent in cross-coupling reactions. By serving as a source of the sulfenyl functional group, this compound can react with various nucleophiles to introduce the sulfur-containing moiety into the target molecule. This reaction pathway is particularly useful in the modification of organic molecules to enhance their chemical and physical properties.Furthermore, benzyl(4-bromophenyl)sulfane can also participate in substitution reactions, where the bromine atom serves as a leaving group, enabling the introduction of the benzylsulfanyl group into different chemical environments. This versatility makes it a valuable tool in the synthesis of sulfur-containing compounds, which often exhibit interesting biological activities and industrial applications.Overall, the use of benzyl(4-bromophenyl)sulfane in chemical synthesis opens up a wide range of possibilities for the creation of new organic molecules with diverse structures and functionalities. Its unique reactivity and compatibility with various synthetic protocols make it a valuable reagent for the construction of complex molecular architectures in organic chemistry research and development.
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GHS Pictogram
Signal Word Danger
UN# 3077
Hazard Statements H410
Precautionary Statements P273-P501
Class 9
Packing Group

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