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CRH6N2 See also: benzene with freshly precipitated mercuric See also: oxide
.
The solution is filtered and the hydrochloride of the See also: base precipitated by alcoholic hydrochloric acid; the See also: free base is obtained as an oil by adding See also: caustic soda
.
It may be obtained in See also: white silky needles, melting at 24-25° C. and containing a molecule of
See also: ether of See also: crystallization by cooling the oil dissolved in ether
.
The free base melts at 39° C
.
It is a strong base, forming See also: stable salts with See also: mineral acids, and is easily soluble in See also: water and in the ordinary organic solvents
.
It has a taste resembling that of See also: chloral See also: hydrate, and leaves a See also: sharp irritation for some See also: time on the See also: tongue; it is also very poisonous (M
.
Busch and A
.
Rast, Berichte, 1897, 30, p
.
521)
.
See also: Cinnolin derivatives are obtained from oxycinnolin carboxylic acid, which is formed by digesting orthophenyl propiolic acid diazo chloride with water
.
Oxycinnolin carboxylic acid on See also: heating gives oxycinnolin, melting at 2250, which with phosphorus pentachloride gives chlorcinnolin
.
This substance is reduced by iron filings and sulphuric acid to dihydrocinnolin
.
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