| Weight | 142.286 g/mol |
|---|---|
| Formula | C10H22 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
2,2-Dimethyloctane (15869-87-1)
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- Synthesis of the four stereoisomers of 2,6-dimethyloctane-1,8-dioic acid, a component of the copulation release pheromone of the cowpea weevil, Callosobruchus maculatus. (Bioscience, Biotechnology, and Biochemistry, 2005)
- Highly Selective Route to Unsymmetrically Substituted 1{2[(Butylsulfanyl)methyl]5(chloromethyl)4methoxyphenoxy}3,7dimethyloctane and Isomers toward Synthesis of Conjugated Polymer OC1C10 Used in LEDs: Synthesis and Optimization (Helvetica Chimica Acta, 2000)
- Reactions of aliphatic halides with solutions of alkali metals in liquid ammonia: III. The reduction of optically active 6-chloro-2,6-dimethyloctane to the corresponding hydrocarbon (Recueil des Travaux Chimiques des Pays-Bas, 2010)
- Stereochemical Studies of the Electrolytic Reactions of Organic Compounds. II. Electrolytic Reduction of Optically Active 6-Chloro-2,6-dimethyloctane to the Corresponding Alkane (Bulletin of the Chemical Society of Japan, 1977)
- Shock tube and modeling study of 2,7-dimethyloctane pyrolysis and oxidation (Combustion and Flame, 2015)
- 4 Acyclic Monoterpene Alcohols with a 2,6-Dimethyloctane Skeleton (1982)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCCCC(C)(C)C
-
InChIKeyGPBUTTSWJNPYJL-UHFFFAOYSA-N
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