1067-14-7 Usage
General Description
Light peach-colored powder.
Air & Water Reactions
Slightly water soluble.
Reactivity Profile
Organometallics, such as TRIETHYLLEAD CHLORIDE, are reactive with many other groups. Incompatible with acids and bases. Organometallics are good reducing agents and therefore incompatible with oxidizing agents. Often reactive with water to generate toxic or flammable gases.
Fire Hazard
The flash point of TRIETHYLLEAD CHLORIDE has not been determined, but TRIETHYLLEAD CHLORIDE is probably combustible.
Safety Profile
Poison by
intraperitoneal, subcutaneous, parenteral,
and intravenous routes. An experimental
teratogen. Experimental reproductive
effects. Mutation data reported. When
heated to decomposition it emits very toxic
fumes of Cland Pb. See also LEAD
COMPOUNDS and CHLORIDES.
Check Digit Verification of cas no
The CAS Registry Mumber 1067-14-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1067-14:
(6*1)+(5*0)+(4*6)+(3*7)+(2*1)+(1*4)=57
57 % 10 = 7
So 1067-14-7 is a valid CAS Registry Number.
InChI:InChI=1/3C2H5.ClH.Pb/c3*1-2;;/h3*1H2,2H3;1H;/q;;;;+1/p-1/rC6H15Pb.ClH/c1-4-7(5-2)6-3;/h4-6H2,1-3H3;1H/q+1;/p-1
1067-14-7Relevant articles and documents
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Hurd,Austin
, p. 1543,1546 (1931)
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Gelius
, p. 297,304 (1970)
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REACTIVITY OF ALLYLIC AND VINYLIC SILANES, GERMANES, STANNANES AND PLUMBANES TOWARD SH2' OR SH2 SUBSTITUTION BY CARBON- OR HETEROATOM-CENTERED FREE RADICALS
Light, James P.,Ridenour, Michael,Beard, Lois,Hershberger, James W.
, p. 17 - 24 (2007/10/02)
Compounds of the type CH2=CHCH2MR3 and (E)-PhCH=CHMR3 (M = Si, Ge, Sn, Pb) were allowed to react with a series of heteroatom-centered radicals (PhY*, Y = S, Se, Te, derived from PhYYPh) and carbon-centered radicals ((CH3)2CH* derived from (CH3)2CHHgCl).We report that alkenylplumbanes and, under forcing conditions, alkenylgermanes undergo SH2 or SH2' substitution of the metal by chain mechanism analogous to those previously reported for alkenylstannanes.Alkenylsilanes are unreactive.Based solely upon product yields, the following trends were observed: The reactivity of the alkenylmetals follow the order metal = Pb > Sn > Ge (> Si).The allylmetals were more reactive then the β-metallostyrenes toward the reactants employed in this study.The chalcogen series PhYYPh exhibits the reactivity order Y = S > Se > Te.
