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  2. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.

  3. tert-Butanesulfinamide - Wikipedia

    en.wikipedia.org/wiki/Tert-Butanesulfinamide

    tert-Butanesulfinamide (also known as 2-methyl-2-propanesulfinamide or Ellman's sulfinamide) is an organosulfur compound and a member of the class of sulfinamides. Both enantiomeric forms are commercially available and are used in asymmetric synthesis as chiral auxiliaries , often as chiral ammonia equivalents for the synthesis of amines .

  4. 1,3,5-Tris(4-(tert-butyl)-3-hydroxy-2,6-dimethylbenzyl)-1,3,5 ...

    en.wikipedia.org/wiki/1,3,5-Tris(4-(tert-butyl...

    Firstly, 2,4-dimethyl-6-tert-butylphenol is reacted with formaldehyde and HCl (Blanc reaction) to generate a chloromethyl group in the less hindered meta position. This intermediate then reacts with cyanuric acid to give the desired product.

  5. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    The effect of the tert-butyl group on the progress of a chemical reaction is called the Thorpe–Ingold effect illustrated in the Diels-Alder reaction below. Compared to a hydrogen substituent, the tert-butyl substituent accelerates the reaction rate by a factor of 240. [2] tert-Butyl effect. The tert-butyl effect is an example of steric hindrance.

  6. Di-tert-butyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butyl_peroxide

    For this reason di-tert-butyl peroxide is commonly used as a radical initiator in organic synthesis and polymer chemistry. The decomposition reaction proceeds via the generation of methyl radicals. (CH 3) 3 COOC(CH 3) 32 (CH 3) 3 CO • (CH 3) 3 CO • → (CH 3) 2 CO + CH • 3 2 CH • 3 → C 2 H 6

  7. Di-tert-butyl ether - Wikipedia

    en.wikipedia.org/wiki/Di-tert-butyl_ether

    2-tert-Butoxy-2-methylpropane Di-tert-butyl ether. Identifiers CAS Number. ... 0.7658 g/cm 3 [2] Melting point: −61 °C (−78 °F; 212 K) [4] Boiling point:

  8. tert-Butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_alcohol

    tert-Butyl alcohol is the simplest tertiary alcohol, with a formula of (CH 3) 3 COH (sometimes represented as t-BuOH). Its isomers are 1-butanol, isobutanol, and butan-2-ol. tert-Butyl alcohol is a colorless solid, which melts near room temperature and has a camphor-like odor. It is miscible with water, ethanol and diethyl ether.

  9. List of additives used for fracking - Wikipedia

    en.wikipedia.org/wiki/List_of_additives_used_for...

    2-Acrylamido-2-methylpropane sulphonic acid sodium salt polymer: Friction reducer 46830-22-2: 2-acryloyloxyethyl(benzyl)dimethylammonium chloride: No record 52-51-7: 2-Bromo-2-nitro-1,3-propanediol: Deodorant, conditioner 111-76-2: 2-Butoxy ethanol: Engine cleaner, degreaser, solvent 1113-55-9: 2-Dibromo-3-nitriloprionamide (2-monobromo-3 ...