方案
97%
表单
solid
mp
133-137 °C (lit.)
SMILES字符串
NC(=O)C(O)c1ccccc1
InChI
1S/C8H9NO2/c9-8(11)7(10)6-4-2-1-3-5-6/h1-5,7,10H,(H2,9,11)
InChI key
MAGPZHKLEZXLNU-UHFFFAOYSA-N
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
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
dust mask type N95 (US), Eyeshields, Gloves
[Molecular biology aspects of the antimicrobial effect of synthetic chemotherapeutic agents].
N Popov
Zeitschrift fur arztliche Fortbildung, 76(15), 662-666 (1982-08-01)
Clemens Lamberth et al.
Pest management science, 62(5), 446-451 (2006-03-22)
Novel types of anti-oomycetic compounds have been designed and prepared. The synthetic approach to these mandelamides is outlined. Biological data demonstrate their high efficacy against important plant diseases such as tomato and potato late blight (Phytophthora infestans De Bary) and
Gonzalo Blay et al.
Organic letters, 8(7), 1287-1290 (2006-03-28)
[reaction: see text] A strategy based on the control of the electron-donating capabilities of the coordinating groups of the ligand has been applied in the catalytic asymmetric addition of organometallic reagents to ketoesters. Mandelamides having deprotonated alcohol and carboxyamido groups
Biank T Gonçalves et al.
Magnetic resonance in chemistry : MRC, 46(5), 418-426 (2008-03-11)
Interesting anisotropic effects were observed for phenylglyoxamides and their respective mandelamides. Such effects were observed in experimental (1)H and (13)C NMR (in CDCl(3), CD(3)OD, and DMSO-d(6) solvents) and in some cases with good correlation to theoretical (1)H and (13)C NMR
Michael J McLeish et al.
Journal of bacteriology, 185(8), 2451-2456 (2003-04-03)
The enzymes of the mandelate metabolic pathway permit Pseudomonas putida ATCC 12633 to utilize either or both enantiomers of mandelate as the sole carbon source. The genes encoding the mandelate pathway were found to lie on a single 10.5-kb restriction
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