63316-81-4

Basic information

• Product Name: Benzene, 1-bromo-4-[(methylthio)methoxy]-
• CAS NO: 63316-81-4
• Molecular Formula: C8H9BrOS
• Molecular Weight: 233.129
• Mol File: 63316-81-4.mol

Chemical Properties

• CAS DataBase Reference: Benzene, 1-bromo-4-[(methylthio)methoxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-bromo-4-[(methylthio)methoxy]-(63316-81-4)
• EPA Substance Registry System: Benzene, 1-bromo-4-[(methylthio)methoxy]-(63316-81-4)

Safety Data

• Hazardous Substances Data: 63316-81-4(Hazardous Substances Data)

Upstream product

• 106-41-2 4-bromo-phenol 
• 2373-51-5 chloro-methylsulfanyl-methane 

Downstream Products

• 496052-51-8 1-(fluoromethoxy)-4-bromobenzene 
• 121824-58-6 4-bromophenyloxymethyl trifluoroacetate 
• 121824-61-1 <(4-bromophenyloxymethyl)thio>methyl acetate 
• 121824-56-4 4-bromophenyloxymethyl acetate 
• 79950-67-7 4-bromobenzyl bromomethyl ether 
• 121824-53-1 bromomethyl 4-bromophenyl ether 
• 35657-04-6 4-bromophenyl chloromethyl ether 
• 1927-95-3 4-bromophenyl acetate 
• 121824-43-9 1-((methylsulfinyl)methoxy)-4-bromobenzene 

Relevant articles and documents

HETEROCYCLE DERIVATIVE HAVING PGD2 RECEPTOR ANTAGONIST ACTIVITY

The present invention is related to a compound represented by formula (I), wherein X1, X2, X3, X4, X5, R5, R6, R7, R8, n, p, q, ring A and ring B are as described in the specification, or a

Syntheses of Sulfinylmethyl Ethers and Conversion of these into Halomethyl and Acyloxymethyl Ethers

Halomethyl ethers can be prepared from sulfinyl ethers by cleavage of the carbon-sulfur bond with thionyl chloride, acetyl chloride or trimethylsilyl halides.In the presence of alkenyl groups in the substrate, acetyl chloride is the reagent of choice.Trifluoroacetic anhydride reacts in the same manner to form the trifluoroacetoxymethyl ether.With acetic anhydride, catalysis by methanesulfonic acid was required.At elevated temperatures in the presence of sodium acetate the products were formed by the Pummerer rearrangement.