质量水平
方案
98%
表单
solid
旋光性
[α]20/D +19°, c = 1 in ethanol
mp
122-124 °C (lit.)
官能团
carboxylic acid
hydroxyl
phenyl
SMILES字符串
O[C@H](Cc1ccccc1)C(O)=O
InChI
1S/C9H10O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8,10H,6H2,(H,11,12)/t8-/m1/s1
InChI key
VOXXWSYKYCBWHO-MRVPVSSYSA-N
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应用
用于制备抑胃酶氨酸的手性结构单元。用于制备降血糖药恩格列酮以及 15N-标记的苯丙氨酸的原料。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Journal of Heterocyclic Chemistry, 29, 431-431 (1992)
Urban, F.J. et al.
Journal of Heterocyclic Chemistry, 29, 431-431 (1991)
Degerbeck, F. et al.
Journal of the Chemical Society. Perkin Transactions 1, 11-11 (1993)
Danilo Christen et al.
Journal of agricultural and food chemistry, 53(18), 7043-7051 (2005-09-01)
Eutypine, 4-hydroxybenzaldehyde, and 3-phenyllactic acid are some of the phytotoxins produced by the pathogens causing Eutypa dieback and esca disease, two trunk diseases of grapevine (Vitis vinifera). Known biocontrol agents such as Fusarium lateritium and Trichoderma sp. were screened for
Mariana-Carmen Chifiriuc et al.
Roumanian archives of microbiology and immunology, 68(1), 27-33 (2009-06-11)
The discovery of intra- and intercellular communication systems (quorum sensing systems) regulating bacterial virulence has afforded a novel opportunity to control infectious bacteria, without interfering with their growth. In this study, we investigated the ability of subinhibitory concentrations (sIC) of
Chromatograms
application for HPLC
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