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| | 4-CHLOROMERCURIBENZOIC ACID Basic information |
| | 4-CHLOROMERCURIBENZOIC ACID Chemical Properties |
| | 4-CHLOROMERCURIBENZOIC ACID Usage And Synthesis |
| Chemical Properties | 4-CHLOROMERCURIBENZOIC ACID is White Solid | | Uses | 4-CHLOROMERCURIBENZOIC ACID can be used to inhibit some enzymes that require unmodified cysteine residues (e.g., adenylyl cyclase). | | Uses | A useful sulfhydryl reagent that reacts with Histidine 225C, a residue of the NhaA-Na/H Antiporter of Escherichia Coli | | Definition | ChEBI: P-chloromercuribenzoic acid is a mercuribenzoic acid and a chlorine molecular entity. It is functionally related to a benzoic acid. | | Safety Profile | Poison by
intraperitoneal route. See also MERCURY
COMPOUNDS. When heated to
decomposition it emits very toxic fumes of
Cland Hg. | | Purification Methods | Its suspension in water is stirred with enough 1M NaOH to dissolve most of it: a small amount of insoluble matter is removed by centrifugation. The chloromercuribenzoic acid is then precipitated by adding 1M HCl and centrifuged off. The precipitation is repeated twice. Finally, the precipitate is washed three times with distilled water (by centrifugation), then dried in a thin layer under vacuum over P2O5 [Boyer J Am Chem Soc 76 4331 1954]. Chloromethylphosphonic acid dichloride [1983 -26 -2] M 167.4, b 50o/0.5mm, 52 -53(59)o/2mm, 63-65o/3mm, 78 -79o/10mm, 87 -88o/15mm, 102-103o/30mm, d 4 1.638, n D 1.4971. It is fractionally distilled using a short Claisen column and redistilled. The aniline salt has m 199-201o. The 3 1P NMR has a single peak at -38±2 ppm from 85% H3PO4. [Kinnear & Perren J Chem Soc 3437 1952, NMR: van Wazer et al. J Am Chem Soc 78 5715 1956, McConnell et al. J Org Chem 22 462 1957, Beilstein 1 III 2593, 1 IV 3068.] |
| | 4-CHLOROMERCURIBENZOIC ACID Preparation Products And Raw materials |
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