推荐产品
质量水平
检测方案
98%
形式
solid
bp
151 °C/16 mmHg (lit.)
mp
45-48 °C (lit.)
SMILES字符串
[H]C(=O)c1cc(OC)cc(OC)c1
InChI
1S/C9H10O3/c1-11-8-3-7(6-10)4-9(5-8)12-2/h3-6H,1-2H3
InChI key
VFZRZRDOXPRTSC-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
应用
常用作合成砌块。
WGK
WGK 3
闪点(°F)
>233.6 °F
闪点(°C)
> 112 °C
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Organic letters, 9(11), 2151-2153 (2007-05-08)
A new poly(ethylene glycol)-modified DAT2-Cu(OAc)2 complex smoothly catalyzes a base-free nitroaldol condensation in a highly enantioselective manner (ee up to 93%) also in reagent-grade solvent and in the presence of air. Effective recovery and recycling (up to five runs) of
Oncology letters, 16(1), 654-659 (2018-06-22)
Despite partial advances in therapy for patients suffering from head and neck squamous cell carcinomas (HNSCC), prognosis still remains poor with minimal improvement in survival for over the last several decades. Some agents found are known to cause cancer cell
Bioprocess and biosystems engineering, 41(7), 973-989 (2018-03-28)
Four bacterial EPSs extracted from Rhizobium leguminosarum bv. trifolii Rt24.2, Sinorhizobium meliloti Rm1021, Bradyrhizobium japonicum USDA110, and Bradyrhizobium elkanii USDA76 were determined towards their metal ion adsorption properties and possible modification of Cerrena unicolor laccase properties. The highest magnesium and
Organic letters, 9(14), 2717-2719 (2007-06-15)
A strategy for ketone synthesis with cyclopropanols as intermediates and its application to (+)-spirolaxine methyl ether is described. The synthesis also features an application of Fu's alkyl-alkyl Suzuki coupling.
Biotechnology progress, 35(6), e2868-e2868 (2019-06-18)
The kinetic description of enzyme-catalyzed reactions is a core task in biotechnology and biochemical engineering. In particular, mechanistic kinetic models help from the discovery of the biocatalyst throughout its application. Chemo- or enantioselective enzyme reactions often undergo two alternative pathways
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门