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  2. Chlorotoluene - Wikipedia

    en.wikipedia.org/wiki/Chlorotoluene

    1-chloro-2-methylbenzene 1-chloro-3-methylbenzene 1-chloro-4-methylbenzene Molecular formula: C 7 H 7 Cl (C 6 H 4 ClCH 3) Molar mass: 126.586 g/mol Appearance colorless liquid CAS number [95-49-8] [108-41-8] [106-43-4] Properties Density and phase: 1.073 g/ml, liquid 1.072 g/ml, liquid 1.069 g/ml, liquid Solubility in water: practically ...

  3. Ethyltoluene - Wikipedia

    en.wikipedia.org/wiki/Ethyltoluene

    Ethyltoluene describes organic compounds with the formula CH 3 C 6 H 4 CH 2 CH 3. Three isomers exist: 1,2- 1,3-, and 1,4-. All are colorless liquids, immiscible in water, with similar boiling points. They are classified are aromatic hydrocarbons. The ring bears two substituents: a methyl group and an ethyl group. [1]

  4. 2-Chloro-6-fluorotoluene - Wikipedia

    en.wikipedia.org/wiki/2-Chloro-6-fluorotoluene

    2-Chloro-6-fluorotoluene (CFT) is a halogenated derivative of toluene that is used as an intermediate in numerous organic syntheses. [1] [2] Uses.

  5. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  6. Dichlorotoluene - Wikipedia

    en.wikipedia.org/wiki/Dichlorotoluene

    Purification is challenging because the individual isomers have similar properties. The 2,6 and 3,5 isomers do not form acceptably from toluene or chlorotoluenes, so these isomers are prepared by indirect methods. For example, 2,6-dichlorotoluene can be prepared by chlorination of 4-toluenesulfonyl chloride followed by desulfonation. [1]

  7. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    H 2 C=CH 2 + HCl → CH 3 CH 2 Cl. In oxychlorination, hydrogen chloride instead of the more expensive chlorine is used for the same purpose: CH 2 =CH 2 + 2 HCl + 12 O 2 → ClCH 2 CH 2 Cl + H 2 O. Secondary and tertiary alcohols react with hydrogen chloride to give the corresponding chlorides.

  8. Chloroethyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Chloroethyl_chloroformate

    Chloroethyl chloroformates (chemical formula: C 3 H 4 Cl 2 O 2) are a pair of related chemical compounds. They can be used to form protecting groups and as N-dealkylating agents. [1] They are listed as extremely hazardous substances. [2]

  9. DMTMM - Wikipedia

    en.wikipedia.org/wiki/DMTMM

    DMTMM (4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methyl-morpholinium chloride) is an organic triazine derivative commonly used for activation of carboxylic acids, particularly for amide synthesis. Amide coupling is one of the most common reactions in organic chemistry and DMTMM is one reagent used for that reaction.