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法的情報
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
保管分類コード
11 - Combustible Solids
WGK
WGK 1
引火点(°F)
257.0 °F - closed cup
引火点(℃)
125 °C - closed cup
個人用保護具 (PPE)
dust mask type N95 (US), Eyeshields, Gloves
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
D131350-BULK:
D131350-10KG:
D131350-1KG:
D131350-VAR:
D131350-5G:
D131350-100G:
D131350-500G:
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D W Kim et al.
Organic letters, 3(3), 445-447 (2001-06-29)
[figure: see text] Fused 1,4-dimethoxybenzenes could be oxidized to benzoquinones by either direct oxidation or demethylation-oxidation. The oxidative demethylation of 5,8-dimethoxy-2-methylquinoline using 1.1 equiv of NBS in aqueous THF and a catalytic amount of H2SO4 at 20 degrees C for
M Masuda et al.
Bioscience, biotechnology, and biochemistry, 60(5), 806-810 (1996-05-01)
Bovine serum albumin (BSA) added to the reaction medium for the oxidative demethylation of 4-methoxyanisole and its "di-CD3" isotopomer ([d6]methoxyanisole), when catalyzed by liver microsomes from untreated rats, decreased the Km values and increased the V(max)/Km (= V/K) values. The
H J Altmann et al.
Archives of toxicology. Supplement. = Archiv fur Toxikologie. Supplement, 8, 114-116 (1985-01-01)
Butylated hydroxyanisole (BHA) is widely used as an antioxidant in foodstuffs, in materials which come into contact with food and also in cosmetic products. The safety of BHA was questioned, however, when it was reported that in a recent Japanese
Tiantian Li et al.
The journal of physical chemistry. A, 115(19), 4988-4994 (2011-04-27)
The effect of substituents on the oxidation potential for the one-electron reaction of 1,4-dimethoxybenzene was understood with a theoretical calculation based on density functional theory (DFT) at the level of B3LYP/6-311+G(d). It is found that the oxidation potential for the
Koji Midorikawa et al.
Chemical communications (Cambridge, England), (36)(36), 3794-3796 (2006-09-14)
Selective monoiodination of aromatic compounds such as dimethoxybenzene has been successfully achieved with I+, which is generated by anodic oxidation of I2 in acetonitrile, using micromixing.
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