543-63-5

Basic information

• Product Name: N-BUTYLMERCURIC CHLORIDE
• Synonyms: N-BUTYLMERCURIC CHLORIDE;Butylchloromercury(II);n-Butyl mercury chloride
• CAS NO: 543-63-5
• Molecular Formula: C₄H₉ClHg
• Molecular Weight: 293.16
• Mol File: 543-63-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 130°
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /solid
• Density: g/cm³
• CAS DataBase Reference: N-BUTYLMERCURIC CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-BUTYLMERCURIC CHLORIDE(543-63-5)
• EPA Substance Registry System: N-BUTYLMERCURIC CHLORIDE(543-63-5)

Safety Data

• Hazardous Substances Data: 543-63-5(Hazardous Substances Data)

Usage

Purification Methods

Crystallise it from 95% EtOH. [Larock & Brown J Am Chem Soc 92 2467 1970, Marvel et al. J Am Chem Soc 47 3009 1925.]

InChI:InChI=1/C4H9.ClH.Hg/c1-3-4-2;;/h1,3-4H2,2H3;1H;/q;;+1/p-1/rC4H9ClHg/c1-2-3-4-6-5/h2-4H2,1H3

Upstream product

• 56-23-5 tetrachloromethane 
• 629-35-6 dibutylmercury 
• 80937-33-3 oxygen 
• 1072-85-1 o-fluorobromobenzene 
• 64248-56-2 1-bromo-2,6-difluorobenzene 
• 1461-25-2 tetra-n-butyltin(IV) 

Downstream Products

• 1075-75-8 butyl-phenyl-mercury 
• 629-35-6 dibutylmercury 
• 5058-19-5 2-butylpyridine 
• 5335-75-1 4-butylpyridine 
• 39178-69-3 rac-3-butylcyclohexanone 
• 76915-10-1 cis-3-butyl-5-methylcyclohexanone 
• 76915-10-1 trans-5-methyl-3-butylcyclohexanone 
• 1129-65-3 (hex-1-yn-1-yl)benzene 
• 6111-82-6 1-phenylhex-1-ene 
• 39576-10-8 2-methyl-1-phenylheptan-1-one 
• 16823-63-5 phenyl hexyl sulfone 
• 16165-66-5 diethyl hexylphosphonate 
• 1461-22-9 tributyltin chloride 
• 111823-21-3 n-butyl(Z-2-phenylethenyl)mercury 

Relevant articles and documents

Investigations on syntheses and reactions of fluorophenylmercury compounds with the ligands 2-FC6H4, 2,6-F2C6H3, and 2,4,6-F3C6H2

2,6-F2C6H3HgCl and 2,4,6-F3C6H2HgCl are synthesized via the reactions of the corresponding phenylmagnesium compounds and HgCl2. 2-FC6H4HgCl is selectively obtained only in a reaction involving intermediately formed Cd(2-FC6H4)2. The diphenylmercury derivative Hg(2,4,6-F3C6H2)2 is obtained while stirring a dichloromethane solution of 2,4,6-F3C6H2HgCl for several days. The direct mercuration of 1,3,5-trifluorobenzene with Hg(OCOCF3)2 yields, depending on the stoichiometry, 2,4,6-trifluorophenylmercury trifluoroacetate and 1,3-bis(trifluoroacetatomercuri)-2,4,6-trifluorobenzene which is converted into the corresponding chloromercuri derivative by treatment with hydrochloric acid in CH3CN. As a product of the reaction of 1,3,5-trifluorobenzene and HgO in CH3OOH only 2,4,6-trifluorophenylmrcury acetate is isolated although spectroscopic evidence has been found for double and triple mercurated derivatives. All compounds are characterized by elemental analyses, nmr and mass spectra. Th reaction of Hg(2,4,-F3C6H2)Cl and Cd(CF3)2 · 2 CH3CN gives Hg(2,4,6-F3C6H2)CF3 which slowly dismutates in CH2Cl2 solution into Hg(2,4,6-F3C6H2)2 and Hg(CF3)2. The ligand exchange of Hg(2,4,6-F3C6H2)2 and TeCl4 selectively gives Te(2,4,6-F3C6H2)2Cl2 and Hg(2,4,6-F3C6H2)Cl. Transmetalations of Hg(2,4,6-F3C6H2)2 and gallium or tin give NMR spectroscopic evidence for the new derivates Ga(2,4,6-F3C6H2)3 and Sn(2,4,6-F3C6H2)4.

INFLUENCE OF OXYGEN ON THE REACTIONS OF ORGANOMERCURY COMPOUNDS WITH POLYCHLOROMETHANES

-