Detail of "1012-72-2"

Reference

Nuclear versus side-chain bromination of tert-butylbenzene

Nuclear versus side-chain bromination of tert-butylbenzene. Bolton, Roger; Bhanger, M. Iqbal; Williams, Gareth H. (Bourne Lab., R. Hollway Bedford Coll., Survey, UK). Sind Univ. Res. J., Sci. Ser., 16(2), 27-34 (English) 1984. CODEN: SURJAA. ISSN: 0080-9624. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) Free radical bromination of Me3CPh (I), studied at 25° using UV light as the source of Br radicals, gave monobromo derivs. of I. o-, m- And p-(Me3C)2C6H4 formed as side-products. No side-chain substitution product was found.Except for chemicals metioned above, 1012-72-2 is also used. .

Vibrational spectra and ir dichroism of p-di(tert-butyl)benzene

Vibrational spectra and ir dichroism of p-di(tert-butyl)benzene. Dobos, S.; Szabo, A.; Zelei, B. (Res. Lab. Inorg. Chem., Budapest, Hung.).Some commonly used reagents like 1012-72-2 is used in this experiment. Spectrochim. Acta, Part A, 32A(7), 1401-8 (English) 1976. CODEN: SAMCAS. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) The ir spectra of p-(Me3C)2C6H4 in the vapor phase, soln., and in KI pellets, and the polarized ir spectra of oriented cryst. films are reported at 200-4000 cm-1. Raman spectra of the soln. and cryst. states are also reported. The internal vibrations of the benzene ring and the Me3C group in the vapor and soln. states have D2h and C3v symmetry, resp., but a decrease in symmetry is obsd. in the cryst. state. The polarized ir spectra are discussed in terms of the oriented gas model and assignment of the mol. vibrations is given. A weak interaction of the neighboring mols. is obsd. in the ring and Me-group vibrations. .