Hulisz, Stanislaw’s team published research in Przemysl Chemiczny in 1979 | CAS: 2525-05-5

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities. Product Details of 2525-05-5

Product Details of 2525-05-5On March 31, 1979, Hulisz, Stanislaw; Wawek, Janina published an article in Przemysl Chemiczny. The article was 《Study on the effectiveness of inhibiting furfural autoxidation》. The article mentions the following:

Furfural autoxidation was inhibited by adding 0.01 weight% p-HOC6H4NH2, N(CH2CH2OH)3, 3,4-(HO)2C6H3Bu, HCONH2 or p-(HO)2C6H4. The effectiveness of the additives decreased in the stated order of compounds; the 1st 3 are recommended. The experimental part of the paper was very detailed, including the reaction process of 4-Butylbenzene-1,2-diol(cas: 2525-05-5Product Details of 2525-05-5)

4-Butylbenzene-1,2-diol(cas: 2525-05-5) belongs to organoboron compounds. Organoboron compounds are versatile intermediates and as such are some of the most important classes of reagents in modern organic chemistry. Organoboron compounds are less toxic than organostannane reagents, and unlike alkynylzinc and magnesium, many organoboron compounds possess remarkable oxidative and thermal stabilities. Product Details of 2525-05-5

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