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It has the chemical formula (CH 3) 2 CHCH(CH 3) 2. It is a colorless liquid which boils at 57.9 °C. It is a colorless liquid which boils at 57.9 °C. References
Chemical formula Name CAS number N 2 H 4: hydrazine: 302-01-2 HNO 3: nitric acid: 7697-37-2 H 2 O 2: hydrogen peroxide: 7722-84-1 HF: hydrofluoric acid: 7664-39-3 H 2 ...
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
[CoCl(NH 3) 5]Cl 2 pentaamminechloridocobalt(3+) chloride where ammine (NH 3)precedes chloride. The central atom name(s) come after the ligands. Where there is more than one central atom it is preceded by di- tri-, tetra- etc. Os 3 (CO) 12, dodecacarbonyltriosmium; Where there are different central atoms they are sequenced using the ...
The alkyl (R') group is named first. The R−C(=O)O part is then named as a separate word based on the carboxylic acid name, with the ending changed from "-oic acid" to "-oate" or "-carboxylate" For example, CH 3 CH 2 CH 2 CH 2 COOCH 3 is methyl pentanoate, and (CH 3) 2 CHCH 2 CH 2 COOCH 2 CH 3 is ethyl 4-methylpentanoate.
2,3-Dimethyl-1-butene is an organic compound with the formula CH 2 =C(CH 3)CH(CH 3) 2. Like the other isomers of dimethylbutene, it is a colorless liquid. Together with 2,3-dimethyl-2-butene it can be produced by dimerization of propylene. It is a precursor to the commercial fragrance tonalide. [1]
Hydrogen peroxide is a chemical compound with the formula H 2 O 2.In its pure form, it is a very pale blue [5] liquid that is slightly more viscous than water.It is used as an oxidizer, bleaching agent, and antiseptic, usually as a dilute solution (3%–6% by weight) in water for consumer use and in higher concentrations for industrial use.
Dimethylbutadiene, formally referred to as 2,3-dimethyl-1,3-butadiene, is an organic compound with the formula (CH 3) 2 C 4 H 4. It is colorless liquid which served an important role in the early history of synthetic rubber. It is now a specialty reagent.