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Jmol is computer software for molecular modelling chemical structures in 3-dimensions. [2] It is an open-source Java viewer for chemical structures in 3D [3]. The name originated from ava (the programming language) + [mol]ecules, and also the mol file format. JSmol is an implementation in JavaScript of the functionality of Jmol. [4]
Neopentane, also called 2,2-dimethylpropane, is a double-branched-chain alkane with five carbon atoms. Neopentane is a flammable gas at room temperature and pressure which can condense into a highly volatile liquid on a cold day, in an ice bath, or when compressed to a higher pressure.
Neopentyl alcohol can be prepared from the hydroperoxide of diisobutylene. [3] It can also be prepared by the reduction of trimethylacetic acid with lithium aluminium hydride . Neopentyl alcohol was the first described in 1891 by L. Tissier, who prepared it by reduction of a mixture of trimethyl acetic acid and trimethylacetyl chloride with ...
Neopentylamine is an organic compound with the molecular formula (CH 3) 3 CCH 2 NH 2. It is a colorless liquid. The molecule is the primary amine derivative of neopentane, (CH 3) 4 C. Like most alkyl amines, it degrades slowly in air. [1]
n-Butylbenzene is the organic compound with the formula C 6 H 5 C 4 H 9.Of two isomers of butylbenzene, n-butylbenzene consists of a phenyl group attached to the 1 position of a butyl group.
3,5-Dichloroaniline is an organic compound with the formula C 6 H 3 Cl 2 (NH 2). It is one of several isomers of dichloroaniline. It is a colorless solid although commercial samples often appear colored. It is produced by hydrogenation of 3,5-dichloronitrobenzene. [2] It is a precursor to the fungicide vinclozolin.
Karstedt's catalyst is an organoplatinum compound derived from divinyl-containing disiloxane.This coordination complex is widely used in hydrosilylation catalysis. It is a colorless solid that is generally assumed to be a mixture of related Pt(0) alkene complexes.
Samples are typically handled with air-free techniques. Most chemical reactions of nickelocene are characterized by its tendency to yield 18-electron products with loss or modification of one Cp ring. Ni(C 5 H 5) 2 + 4 PF 3 → Ni(PF 3) 4 + organic products. The reaction with secondary phosphines follows a similar pattern: