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质量水平
方案
97%
表单
solid
沸点
140 °C/12 mmHg (lit.)
mp
59-61 °C (lit.)
SMILES字符串
NCCCCCCCCCCN
InChI
1S/C10H24N2/c11-9-7-5-3-1-2-4-6-8-10-12/h1-12H2
InChI key
YQLZOAVZWJBZSY-UHFFFAOYSA-N
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警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Sen-Ichi Aizawa et al.
Chirality, 28(1), 85-91 (2015-10-30)
The optically active mixed-ligand fac(S)-tris(thiolato)rhodium(III) complexes, ΔL -fac(S)-[Rh(aet)2 (L-cys-N,S)](-) (aet = 2-aminoethanethiolate, L-cys = L-cysteinate) () and ΔLL -fac(S)-[Rh(aet)(L-cys-N,S)2 ](2-) were newly prepared by the equatorial preference of the carboxyl group in the coordinated L-cys ligand. The amide formation reaction
Jie Zhang et al.
Journal of biotechnology, 299, 79-85 (2019-05-03)
Glucosinolates can be hydrolyzed by the enzyme commonly known as myrosinase (E.C. 3.2.1.147) to a variety of biological compounds. Myrosinase (MYR) has been immobilized through the flexible spacers of different length on cross-linked chitosan resin (CCR). Ethylene diamine, hexamethylenediamine and
Lei He et al.
Scientific reports, 8(1), 767-767 (2018-01-18)
G-quadruplexes (GQ) folded by the oncogenic G-rich sequences are the promising targets for developing anticancer therapeutic molecules. However, the current drug development mainly focused on non-covalent dynamic binders to stabilize GQ structures, while the covalent targeting from inorganic complexes via
Dmitry V Klinov et al.
Colloids and surfaces. B, Biointerfaces, 196, 111321-111321 (2020-08-26)
High-resolution atomic force microscopy (AFM) of biomacromolecules is a valuable method for structural studies in biology. Traditionally, the surfaces used for AFM imaging of individual molecules are limited to mica, graphite, and glass. Because these substrates have certain shortcomings, new
Gabriela E Davey et al.
Nature communications, 8(1), 1575-1575 (2017-11-18)
The 'acidic patch' is a highly electronegative cleft on the histone H2A-H2B dimer in the nucleosome. It is a fundamental motif for protein binding and chromatin dynamics, but the cellular impact of targeting this potentially therapeutic site with exogenous molecules
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