SMILES string
On1nnc2ccccc12
concentration
<5% in H2O
mp
156-159 °C (lit.)
Biochem/physiol Actions
在使用 DCC 作为缩合剂合成肽时可抑制外消旋化。
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Expl. 1.3 - Eye Irrit. 2
存储类别
1 - Explosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Takayuki Hata et al.
Journal of hazardous materials, 181(1-3), 1175-1178 (2010-07-14)
Carbamazepine (CBZP) is used as an antiepileptic drug and is highly persistent. In this study, CBZP was treated with laccase from white rot fungus Trametes versicolor in the presence of a redox mediator 1-hydroxybenzotriazole (HBT). A single treatment with laccase
Liqiang Tian et al.
International journal of biological macromolecules, 50(3), 782-787 (2011-12-14)
This study evaluates the bleaching efficiency of the hydrogen peroxide bleaching process combined with laccase-mediated system pretreatment (LMS-HPBP) in the treatment of scoured cotton fabric. By changing the factors of laccase-mediated system pretreatment and the hydrogen peroxide bleaching process and
Akira Kawamura et al.
Bioorganic & medicinal chemistry, 16(19), 8824-8829 (2008-09-19)
Benzophenone photophores are employed widely for photoaffinity-labeling studies. Photolabeling with benzophenone, however, is hardly a routine experiment. Even when a photoprobe binds to its target, photocrosslinking does not necessarily occur. This is because photolabeling by benzophenone is affected by many
Thitinard Nitheranont et al.
Bioscience, biotechnology, and biochemistry, 75(9), 1845-1847 (2011-09-08)
A major laccase isozyme from Grifola frondosa (Lac 1) was found to be effective for decolorizing of synthetic dyes and degrading of bisphenol A. The oxidative capability of Lac 1 toward synthetic dyes and bisphenol A was enhanced in the
Pierluigi Plastina et al.
Natural product research, 26(19), 1799-1805 (2011-10-13)
Four analogues of ochratoxin A (OTA) differing for the aminoacidic moiety were synthesised using ochratoxin α (OTα) as the starting material. The condensation reaction between protected amino acids and OTα, carried out in the presence of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC • HCl) and
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