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  2. Neopentane - Wikipedia

    en.wikipedia.org/wiki/Neopentane

    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.

  3. Neopentylamine - Wikipedia

    en.wikipedia.org/wiki/Neopentylamine

    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]

  4. Jmol - Wikipedia

    en.wikipedia.org/wiki/Jmol

    JSmol is an implementation in JavaScript of the functionality of Jmol. [4] It can hence be embedded in web pages to display interactive 3D models of molecules and other structures without the need for any software apart from the web browser (it does not use Java).

  5. Neopentyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_alcohol

    Neopentyl alcohol is a compound with formula (CH 3) 3 CCH 2 OH. It is a colorless solid. It is a colorless solid. The compound is one of the eight isomers of pentyl alcohol .

  6. Isopentane - Wikipedia

    en.wikipedia.org/wiki/Isopentane

    2 (C 2 H 5). Isopentane is a volatile and flammable liquid. It is one of three structural isomers with the molecular formula C 5 H 12, the others being pentane (n-pentane) and neopentane (2,2-dimethylpropane). Isopentane is commonly used in conjunction with liquid nitrogen to achieve a liquid bath temperature of −160 °C.

  7. Neopentyl glycol diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_glycol...

    It is aliphatic and a colorless liquid. It has the formula C 11 H 20 O 4 and the CAS registry number of 17557-23-2. [2] It has two oxirane groups per molecule. [3] Its principle use is in modifying epoxy resins. [4] It is REACH registered. [5] The IUPAC name is 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane. [6]

  8. Neophyl chloride - Wikipedia

    en.wikipedia.org/wiki/Neophyl_chloride

    c 6 h 5 c(ch 3) 2 ch 2 oh + socl 2 → c 6 h 5 c(ch 3) 2 ch 2 cl + hcl + so 2 It is easily prepared on a large scale from benzene and methallyl chloride by an electrophilic aromatic substitution reaction, using sulfuric acid as the catalyst : [ 4 ] The reaction is an example of an electrophilic aromatic substitution reaction.

  9. n-Butylbenzene - Wikipedia

    en.wikipedia.org/wiki/N-Butylbenzene

    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.